- Preparation of unsaturated cyclic alcohols from aldehydes, Japan, , ,
Cas no 95-12-5 (Bicyclo2.2.1hept-5-en-2-ylmethanol)
95-12-5 structure
Product Name:Bicyclo2.2.1hept-5-en-2-ylmethanol
CAS No:95-12-5
MF:C8H12O
MW:124.180282592773
MDL:MFCD00167571
CID:34777
PubChem ID:78946
Update Time:2024-10-25
Bicyclo2.2.1hept-5-en-2-ylmethanol Chemical and Physical Properties
Names and Identifiers
-
- Bicyclo[2.2.1]hept-5-en-2-ylmethanol
- 5-Norbornene-2-methanol,mixture of endo and exo
- 2-Hydroxymethyl-5-norbornene
- 5-Norborene-2-methanol
- 5-norbornene-2-methanol(NMO)mixture of endo and exo
- 5-Norbornen-2-methanol (mixture of isomers)
- 5-Norbornene-2-methanol
- 5-bicyclo[2.2.1]hept-2-enylmethanol
- Bicyclo[2.2.1]hept-5-ene-2-methanol (mixture of isomers)
- Bicyclo[2.2.1]hept-5-ene-2-methanol
- Cyclol
- 5-Hydroxymethyl-2-norbornene
- 5-Norbornene 2-methanol
- Bicyclo(2.2.1)hept-5-ene-2-methanol
- 5-Hydroxymethylbicyclo(2.2.1)hept-2-ene
- 2-(Hydroxymethyl)bicyclo(2.2.1)hept-5-ene
- LUMNWCHHXDUKFI-UHFFFAOYSA-N
- 5-Hydroxymethylbicyclo[2.2.1]hept-2-ene
- 2-(Hydroxymethyl)bicyclo[2.2.1]hept-5-ene
- norbornen-5-methanol
- 5-norbornen-
- 5-Norbornene-2-methanol (6CI, 7CI, 8CI)
- 2-Norbornen-5-methanol
- 5-(Hydroxymethyl)bicyclo[2.2.1]hept-2-ene
- [Bicyclo[2.2.1]hept-5-en-2-yl]methanol
- Norbornene-5-methyl alcohol
- NSC 403110
- DTXSID3038698
- N43L8J2KTL
- DB-003096
- NS00040437
- DS-18405
- UNII-N43L8J2KTL
- NSC-403110
- AKOS009156947
- J-802157
- SY015570
- 30421-42-2
- STL563998
- F1995-0286
- AI3-08981
- bicyclo-[2,2,1]-hept-5-en-2-yl-methyl alcohol
- EN300-246230
- Bicyclo[2.2.1]5-heptene-2-methanol
- EINECS 202-392-0
- (4s)-bicyclo[2.2.1]hept-5-en-2-ylmethanol
- FD14041
- 2-bicyclo[2.2.1]hept-5-enylmethanol
- NSC403110
- MFCD00167571
- F16263
- Exo-5-norbornene-2-methanol(exo)
- SCHEMBL33077
- N0979
- 5-norbornen-2-methanol
- 95-12-5
- 5-Norbornene-2-yl methanol
- {bicyclo[2.2.1]hept-5-en-2-yl}methanol
- CS-0114684
- 5-norbornen -2-methanol
- 5-Norbornene-2-methanol, mixture of isomers
- 5-hydroxy methyl-2-norbornene
- Bicyclo2.2.1hept-5-en-2-ylmethanol
-
- MDL: MFCD00167571
- Inchi: 1S/C8H12O/c9-5-8-4-6-1-2-7(8)3-6/h1-2,6-9H,3-5H2
- InChI Key: LUMNWCHHXDUKFI-UHFFFAOYSA-N
- SMILES: OCC1C2CC(C=C2)C1
Computed Properties
- Exact Mass: 124.08900
- Monoisotopic Mass: 124.089
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 9
- Rotatable Bond Count: 1
- Complexity: 140
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 3
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 20.2
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: 1.2
Experimental Properties
- Color/Form: Not determined
- Density: 1.027?g/mL?at 25?°C(lit.)
- Boiling Point: 97?°C/20?mmHg(lit.)
- Flash Point: Fahrenheit: 188.6 ° f < br / > Celsius: 87 ° C < br / >
- Refractive Index: n20/D 1.500(lit.)
- PSA: 20.23000
- LogP: 1.19090
- Solubility: Not determined
- Vapor Pressure: 0.2±0.8 mmHg at 25°C
Bicyclo2.2.1hept-5-en-2-ylmethanol Security Information
-
Symbol:
- Prompt:warning
- Signal Word:Warning
- Hazard Statement: H302 + H312 + H332
- Warning Statement: P280
- WGK Germany:3
- Hazard Category Code: 20/21/22
- Safety Instruction: S36/37/39-S45
-
Hazardous Material Identification:
- Storage Condition:Sealed in dry,2-8°C
- Risk Phrases:R20/21/22
Bicyclo2.2.1hept-5-en-2-ylmethanol Customs Data
- HS CODE:2906199090
- Customs Data:
China Customs Code:
2906199090Overview:
2906199090. Other naphthenic alcohols,Cycloenol and cycloterpenol. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:5.5%. general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Summary:
2906199090. cyclanic, cyclenic or cyclotherpenic alcohols. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%
Bicyclo2.2.1hept-5-en-2-ylmethanol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| XI GE MA AO DE LI QI ( SHANG HAI ) MAO YI Co., Ltd. | 248533-5G |
Bicyclo2.2.1hept-5-en-2-ylmethanol |
95-12-5 | 5g |
¥518.46 | 2023-12-09 | ||
| TRC | B789408-50mg |
Bicyclo[2.2.1]hept-5-en-2-ylmethanol |
95-12-5 | 50mg |
$ 50.00 | 2022-06-06 | ||
| TRC | B789408-100mg |
Bicyclo[2.2.1]hept-5-en-2-ylmethanol |
95-12-5 | 100mg |
$ 65.00 | 2022-06-06 | ||
| TRC | B789408-500mg |
Bicyclo[2.2.1]hept-5-en-2-ylmethanol |
95-12-5 | 500mg |
$ 80.00 | 2022-06-06 | ||
| Apollo Scientific | OR315262-5g |
5-Norbornene-2-methanol |
95-12-5 | 99% | 5g |
£15.00 | 2025-02-19 | |
| Apollo Scientific | OR315262-25g |
5-Norbornene-2-methanol |
95-12-5 | 99% | 25g |
£17.00 | 2025-02-19 | |
| Apollo Scientific | OR315262-100g |
5-Norbornene-2-methanol |
95-12-5 | 99% | 100g |
£58.00 | 2025-02-19 | |
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | N0979-5G |
5-Norbornen-2-methanol (mixture of isomers) |
95-12-5 | >98.0%(GC) | 5g |
¥200.00 | 2024-04-15 | |
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | N0979-25G |
5-Norbornen-2-methanol (mixture of isomers) |
95-12-5 | >98.0%(GC) | 25g |
¥675.00 | 2024-04-15 | |
| SHANG HAI BI DE YI YAO KE JI GU FEN Co., Ltd. | BD22265-5g |
Bicyclo[2.2.1]hept-5-en-2-ylmethanol |
95-12-5 | 98% | 5g |
¥22.0 | 2024-04-17 |
Bicyclo2.2.1hept-5-en-2-ylmethanol Production Method
Production Method 1
Production Method 2
Production Method 3
Reaction Conditions
1.1 Reagents: Lithium aluminum hydride Solvents: Tetrahydrofuran ; reflux
Reference
- Mechanochemical ring-opening metathesis polymerization: development, scope, and mechano-exclusive polymer synthesisLee, Gue Seon; Lee, Hyo Won; Lee, Hyun Sub; Do, Taeyang; Do, Jean-Louis; et al, Chemical Science, 2022, 13(39), 11496-11505
Production Method 4
Reaction Conditions
1.1 Reagents: Lithium aluminum hydride
Reference
- Bicontinuous Alkaline Fuel Cell Membranes from Strongly Self-Segregating Block CopolymersPrice, Samuel C.; Ren, Xiaoming; Jackson, Aaron C.; Ye, Yuesheng; Elabd, Yossef A.; et al, Macromolecules (Washington, 2013, 46(18), 7332-7340
Production Method 5
Reaction Conditions
1.1 Reagents: Lithium aluminum hydride Solvents: Dichloromethane , Tetrahydrofuran ; 2 min, 0 °C; 2 h, rt
Reference
- LiAlH4-induced reductive dephosphonylation of α,α-dialkyl triethyl β-phosphonyl esters: mechanistic study and synthetic applicationZhu, Jia-Liang; Bau, Sheng Jr.; Shih, You-Cheng, Synlett, 2012, 23(6), 863-866
Production Method 6
Reaction Conditions
1.1 99 h, pH 4 - 5, 170 - 180 °C
Reference
- Norbornene-containing mannich bases on the basis of aliphatic aminesHajiyeva, G. E.; Mammadbayli, E. H.; Ibrahimli, S. I.; Jafarov, I. A., Azerbaidzhanskii Khimicheskii Zhurnal, 2018, (3), 50-56
Production Method 7
Reaction Conditions
1.1 2 h, 100 - 200 psi, 210 °C
Reference
- High Tg sulfonated insertion polynorbornene ionomers prepared by catalytic insertion polymerizationPierre, Florian; Commarieu, Basile; Tavares, Ana C.; Claverie, Jerome, Polymer, 2016, 86, 91-97
Production Method 8
Reaction Conditions
1.1 Reagents: Lithium aluminum hydride Solvents: Tetrahydrofuran ; 0 °C; 10 h, rt
1.2 Reagents: Hydrochloric acid Solvents: Water ; pH 6, 0 °C
1.2 Reagents: Hydrochloric acid Solvents: Water ; pH 6, 0 °C
Reference
- Ligand Design for Luminescent Lanthanide-Containing Metallopolymersde Bettencourt-Dias, Ana; Rossini, Jeffrey S. K., Inorganic Chemistry, 2016, 55(20), 9954-9963
Production Method 9
Reaction Conditions
1.1 Reagents: Potassium carbonate , Carbon monoxide Catalysts: Tricarbonyl[(1,3,3a,7a-η)-4,5,6,7-tetrahydro-1,3-bis(trimethylsilyl)-2H-inden-2-… Solvents: Dimethyl sulfoxide , Water ; 20 h, 10 bar, 100 °C; 100 °C → rt
1.2 Reagents: Hydrochloric acid Solvents: Water ; 1 h, rt
1.2 Reagents: Hydrochloric acid Solvents: Water ; 1 h, rt
Reference
- Discrete iron complexes for the selective catalytic reduction of aromatic, aliphatic, and α,β-unsaturated aldehydes under water-gas shift conditionsTlili, Anis; Schranck, Johannes; Neumann, Helfried; Beller, Matthias, Chemistry - A European Journal, 2012, 18(50), 15935-15939
Production Method 10
Reaction Conditions
1.1 Reagents: Sodium borohydride ; 20 min, 25 °C
1.2 Reagents: Water ; rt
1.2 Reagents: Water ; rt
Reference
- Sodium Tetraalkoxyborates: Intermediates for the Quantitative Reduction of Aldehydes and Ketones to Alcohols through Ball Milling with NaBH4Naimi-Jamal, M. Reza; Mokhtari, Javad; Dekamin, Mohammad G.; Kaupp, Gerd, European Journal of Organic Chemistry, 2009, (21), 3567-3572
Production Method 11
Reaction Conditions
1.1 Catalysts: Iridium, aqua[[2,2′-bipyridine]-6,6′(1H,1′H)-dionato(2-)-κN1,κN1′][(1,2,3,4,5-η)… Solvents: Isopropanol ; 12 h, 120 °C; 120 °C → rt
Reference
- Transfer Hydrogenation of Aldehydes and Ketones with Isopropanol under Neutral Conditions Catalyzed by a Metal-Ligand Bifunctional Catalyst [Cp*Ir(2,2'-bpyO)(H2O)]Wang, Rongzhou; Tang, Yawen; Xu, Meng; Meng, Chong; Li, Feng, Journal of Organic Chemistry, 2018, 83(4), 2274-2281
Production Method 12
Reaction Conditions
1.1 Reagents: Lithium aluminum hydride Solvents: Tetrahydrofuran ; overnight, rt
1.2 Solvents: Water ; rt
1.2 Solvents: Water ; rt
Reference
- Utilizing thiol-ene chemistry for crosslinked nickel cation-based anion exchange membranesKwasny, Michael T.; Zhu, Liang; Hickner, Michael A.; Tew, Gregory N., Journal of Polymer Science, 2018, 56(3), 328-339
Production Method 13
Reaction Conditions
1.1 Reagents: Sodium carbonate , Chlorosulfonyl isocyanate Solvents: Dichloromethane ; rt; 20 h, reflux; reflux → 0 °C
1.2 Reagents: Sodium hydroxide Solvents: Methanol ; 1 h
1.3 Reagents: Hydrochloric acid Solvents: Water ; neutralized
1.2 Reagents: Sodium hydroxide Solvents: Methanol ; 1 h
1.3 Reagents: Hydrochloric acid Solvents: Water ; neutralized
Reference
- Deprotection of benzyl and p-methoxybenzyl ethers by chlorosulfonyl isocyanate-sodium hydroxideKim, Ji Duck; Han, Gyoonhee; Zee, Ok Pyo; Jung, Young Hoon, Tetrahedron Letters, 2003, 44(4), 733-735
Production Method 14
Reaction Conditions
1.1 Reagents: Hydroquinone ; 19 h, rt → 190 °C
Reference
- Influence of Hydroxyl Group Concentration on Mechanical Properties and Impact Resistance of ROMP CopolymersDennis, Joseph M.; Long, Tyler R.; Krishnamurthy, Ajay ; Tran, Ngon T.; Patterson, Brendan A.; et al, ACS Applied Polymer Materials, 2020, 2(6), 2414-2425
Production Method 15
Reaction Conditions
1.1 9 h, 4 - 5 atm, 170 - 180 °C
Reference
- Synthesis and properties of mannich bases on the basis of norbornenylmethanol, aliphatic amines and benzaldehydeHajiyeva, Gulsum E.; Mammadbayli, Eldar H.; Ibrahimli, Sahil I.; Abiyev, Huseyn A., Neft Kimyasi va Neft E'mali Proseslari, 2020, 21(1), 36-44
Production Method 16
Reaction Conditions
1.1 9 h, 4 - 5 atm, 170 - 180 °C
Reference
- Synthesis of Mannich bases based on norbornenylmethanol, cyclic amines and benzaldehyde and their antimicrobial activityHajiyeva, G. E., Azerbaidzhanskii Khimicheskii Zhurnal, 2019, (3), 68-74
Production Method 17
Reaction Conditions
1.1 9 h, 4 - 5 atm, 170 - 180 °C
Reference
- Norbornene containing Mannich bases on the basis of cyclic aminesHajiyeva, Gulsum E.; Mammadbayli, Eldar H.; Ibrahimly, Sahil I.; Talybov, Gulahmad M., Neft Kimyasi va Neft E'mali Proseslari, 2017, 18(4), 331-340
Production Method 18
Reaction Conditions
1.1 9 h, 4 - 5 atm, 170 - 180 °C
Reference
- Mannich Bases from Bicyclo[2.2.1]hept-5-en-2-ylmethanol, Secondary Amines and FormaldehydeMammadbayli, E. H.; Hajiyeva, G. E.; Ibrahimli, S. I.; Jafarova, N. A., Russian Journal of General Chemistry, 2018, 88(10), 2204-2208
Production Method 19
Reaction Conditions
1.1 Reagents: 1,4-Naphthalenedicarbonitrile Solvents: Acetonitrile , Water
Reference
- Photoinduced single-electron-transfer (set)-initiated oxidative cleavage of benzylic ether protecting group: a mild and efficient procedurePandey, G.; Krishna, A., Synthetic Communications, 1988, 18(18), 2309-14
Production Method 20
Reaction Conditions
1.1 -78 °C; 2 h, -78 °C → rt; rt → 45 °C; 8 h, 45 °C
1.2 Reagents: Sodium hydroxide , Sodium borohydride Solvents: Methanol , Water ; 1 h, rt
1.2 Reagents: Sodium hydroxide , Sodium borohydride Solvents: Methanol , Water ; 1 h, rt
Reference
- Synthesis and Characterization of Lithium-Ion Conductive Membranes with Low Water PermeationStone, David A.; Welna, Daniel T.; Allcock, Harry R., Chemistry of Materials, 2007, 19(10), 2473-2482
Bicyclo2.2.1hept-5-en-2-ylmethanol Raw materials
- 5-Norbornene-2-carboxaldehyde
- Ethyl 2-(diethoxyphosphinyl)bicyclo[2.2.1]hept-5-ene-2-carboxylate
- Bicyclo[2.2.1]hept-2-ene, 5-[(phenylmethoxy)methyl]-
- 5-Norbornen-2-carboxylic acid
- exo-5-Norbornenecarboxylic acid
Bicyclo2.2.1hept-5-en-2-ylmethanol Preparation Products
Bicyclo2.2.1hept-5-en-2-ylmethanol Suppliers
Amadis Chemical Company Limited
Gold Member
(CAS:95-12-5)Bicyclo2.2.1hept-5-en-2-ylmethanol
Order Number:A845189
Stock Status:in Stock
Quantity:500g/1kg
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 07:05
Price ($):151.0/302.0
Email:[email protected]
Suzhou Senfeida Chemical Co., Ltd
Gold Member
(CAS:95-12-5)5-Norbornene-2-methanol
Order Number:sfd10414
Stock Status:in Stock
Quantity:200KG
Purity:99%
Pricing Information Last Updated:Friday, 19 July 2024 14:35
Price ($):discuss personally
Email:[email protected]
Tiancheng Chemical (Jiangsu) Co., Ltd
Gold Member
(CAS:95-12-5)5-降冰片烯-2-甲醇
Order Number:LE20755364
Stock Status:in Stock
Quantity:25KG,200KG,1000KG
Purity:99%
Pricing Information Last Updated:Friday, 20 June 2025 12:48
Price ($):discuss personally
Email:[email protected]
Bicyclo2.2.1hept-5-en-2-ylmethanol Related Literature
-
Albertus D. Handoko,Khoong Hong Khoo,Teck Leong Tan,Hongmei Jin,Zhi Wei Seh J. Mater. Chem. A, 2018,6, 21885-21890
-
Dongjia Han,Bing Xue,Juan Du,Tomohiro Miyatake,Hitoshi Tamiaki,Xin Xing,Wei Yuan,Yanyan Li Phys. Chem. Chem. Phys., 2016,18, 24252-24260
-
Liao Xiaoqing,Li Ruiyi,Li Zaijun,Sun Xiulan,Wang Zhouping,Liu Junkang New J. Chem., 2015,39, 5240-5248
-
Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693
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