- 2,5,7-Trisubstituted benzo[b]furans through a copper- and/or palladium-catalyzed assembly and functionalization processArcadi, Antonio; Blesi, Federico; Cacchi, Sandro; Fabrizi, Giancarlo; Goggiamani, Antonella, Tetrahedron Letters, 2011, 52(40), 5149-5152
Cas no 92-04-6 (3-chloro-1,1'-biphenyl-4-ol)
3-chloro-1,1'-biphenyl-4-ol structure
Product Name:3-chloro-1,1'-biphenyl-4-ol
CAS No:92-04-6
MF:C12H9ClO
MW:204.652262449265
MDL:MFCD00045745
CID:805687
PubChem ID:7074
Update Time:2024-10-26
3-chloro-1,1'-biphenyl-4-ol Chemical and Physical Properties
Names and Identifiers
-
- [1,1'-Biphenyl]-4-ol,3-chloro-
- 4-Biphenylol,3-chloro- (8CI)
- Phenol, 2-chloro-4-phenyl- (6CI,7CI)
- 2-Chloro-p-phenylphenol
- 3-Chloro-4-biphenylol
- 3-Chloro-4-hydroxybiphenyl
- 4-Phenyl-2-chlorophenol
- Dowicide 4
- NSC 3858
- Sanidril
- o-Chloro-p-phenylphenol
- 2-Chloro-4-phenylphenol
- 4-Hydroxy-3-chlorobiphenyl
- 3-Chlorobiphenyl-4-ol
- 3-Chloro-4-hydroxydiphenyl
- Phenol, 2-chloro-4-phenyl-
- 3-Chlor-4-hydroxybifenyl
- 4-Biphenylol, 3-chloro-
- Caswell No. 209
- 3-Chlor-4-hydroxybifenyl [Czech]
- 3-Chloro-(1,1-biphenyl)-4-ol
- 3-Chloro-[1,1'-biphenyl]-4-ol
- EPA Pesticide Chemical Code 062206
- [1,1'-Biphenyl]-4
- 3-Chloro[1,1′-biphenyl]-4-ol (ACI)
- 4-Biphenylol, 3-chloro- (8CI)
- Phenol, 2-chloro-4-phenyl- (6CI, 7CI)
- 3-chloro-1,1'-biphenyl-4-ol
- 3-chloro-4-biphenylo
- dowicide4
- 1,1-Biphenyl-4-ol, 3-chloro-
- 4-BIPHENYLOL,3-CHLORO-
- CHEMBL406630
- NSC-3858
- 3-06-00-03330 (Beilstein Handbook Reference)
- AI3-03935
- InChI=1/C12H9ClO/c13-11-8-10(6-7-12(11)14)9-4-2-1-3-5-9/h1-8,14H
- 3-Chloro[1,1'-biphenyl]-4-ol #
- BRN 1868370
- NS00120596
- D89225
- BIDD:ER0224
- BDBM50376216
- 3-Chloro[1,1a(2)-biphenyl]-4-ol
- Dowcide 4
- [1,1'-Biphenyl]-4-ol, 3-chloro-
- 92-04-6
- (1,1'-Biphenyl)-4-ol, 3-chloro-
- NSC3858
- AS-60605
- WLN: QR BG DR
- AKOS000121184
- 3-chloro-biphenyl-4-ol
- UNII-229K1W6JFY
- CS-0190750
- BZWMYDJJDBFAPE-UHFFFAOYSA-
- EN300-21187
- SCHEMBL1513545
- 229K1W6JFY
- EINECS 202-120-0
- Z104493626
- MFCD00045745
- Q27253643
- 4-PHENYL-2-CHLOROPHENOL [MI]
-
- MDL: MFCD00045745
- Inchi: 1S/C12H9ClO/c13-11-8-10(6-7-12(11)14)9-4-2-1-3-5-9/h1-8,14H
- InChI Key: BZWMYDJJDBFAPE-UHFFFAOYSA-N
- SMILES: ClC1C(O)=CC=C(C2C=CC=CC=2)C=1
Computed Properties
- Exact Mass: 204.03400
- Monoisotopic Mass: 204.0341926g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 14
- Rotatable Bond Count: 1
- Complexity: 177
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 4.3
- Topological Polar Surface Area: 20.2
- Surface Charge: 0
- Tautomer Count: 3
Experimental Properties
- Density: 1.1409 (rough estimate)
- Melting Point: 77.0 to 80.0 deg-C
- Boiling Point: 293.89°C (rough estimate)
- Refractive Index: 1.5990 (estimate)
- PSA: 20.23000
- LogP: 3.71260
3-chloro-1,1'-biphenyl-4-ol Security Information
-
Symbol:
- Prompt:dangerous
- Hazard Statement: H303-H316-H318
- Warning Statement: P280-P305+P351+P338+P310-P312-P332+P313
- Hazard Category Code: 22-36/38
- Safety Instruction: S26; S37/39
- RTECS:DV6650000
- Risk Phrases:R22; R36/38
3-chloro-1,1'-biphenyl-4-ol Customs Data
- HS CODE:2907199090
- Customs Data:
China Customs Code:
2907199090Overview:
2907199090 Other monophenols. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:5.5% general tariff:30.0%
Declaration elements:
Product Name, component content, use to
Summary:
2907199090 other monophenols VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%
3-chloro-1,1'-biphenyl-4-ol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | C869208-5g |
2-Chloro-4-phenylphenol |
92-04-6 | 96% | 5g |
154.00 | 2021-05-17 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | C0263-25g |
3-chloro-1,1'-biphenyl-4-ol |
92-04-6 | 96.0%(GC) | 25g |
¥430.0 | 2022-05-30 | |
| abcr | AB139952-25 g |
2-Chloro-4-phenylphenol, 96%; . |
92-04-6 | 96% | 25g |
€65.60 | 2022-09-01 | |
| TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd. | C0263-25G |
2-Chloro-4-phenylphenol |
92-04-6 | >96.0%(GC) | 25g |
¥295.00 | 2024-04-15 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | PS123-1g |
3-chloro-1,1'-biphenyl-4-ol |
92-04-6 | 96.0%(GC) | 1g |
¥102.0 | 2022-05-30 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | PS123-5g |
3-chloro-1,1'-biphenyl-4-ol |
92-04-6 | 96.0%(GC) | 5g |
¥216.0 | 2022-05-30 | |
| Enamine | EN300-21187-1g |
3-chloro-[1,1'-biphenyl]-4-ol |
92-04-6 | 95% | 1g |
$26.0 | 2023-09-16 | |
| Enamine | EN300-21187-5g |
3-chloro-[1,1'-biphenyl]-4-ol |
92-04-6 | 95% | 5g |
$29.0 | 2023-09-16 | |
| Enamine | EN300-21187-10g |
3-chloro-[1,1'-biphenyl]-4-ol |
92-04-6 | 95% | 10g |
$32.0 | 2023-09-16 | |
| abcr | AB139952-25g |
2-Chloro-4-phenylphenol, 96%; . |
92-04-6 | 96% | 25g |
€69.40 | 2024-04-15 |
3-chloro-1,1'-biphenyl-4-ol Production Method
Production Method 1
Reaction Conditions
1.1 Reagents: Chlorosuccinimide Catalysts: Aluminum chloride Solvents: Dichloromethane ; rt
Reference
Production Method 2
Reaction Conditions
1.1 Reagents: Dimethylhydrazine dihydrochloride Solvents: Acetonitrile ; 120 min, 120 °C
Reference
- Synthesis of o-chlorophenols via an unexpected nucleophilic chlorination of quinone monoketals mediated by N,N'-dimethylhydrazine dihydrochlorideYin, Zhiwei; Zhang, Jinzhu; Wu, Jing; Green, Riana; Li, Sihan; et al, Organic & Biomolecular Chemistry, 2014, 12(18), 2854-2858
Production Method 3
Reaction Conditions
1.1 Reagents: Sodium hydroxide Catalysts: Palladium chloride Solvents: Water
1.2 Reagents: Hydrochloric acid Solvents: Water
1.2 Reagents: Hydrochloric acid Solvents: Water
Reference
- Ligandless palladium catalyzed reactions of arylboronic acids and sodium tetraphenylborate with aryl halides in aqueous mediaBumagin, Nikolai A.; Bykov, Victor V., Tetrahedron, 1997, 53(42), 14437-14450
Production Method 4
Reaction Conditions
1.1 Reagents: N-Chloro-N-(phenylsulfonyl)benzenesulfonamide Solvents: Acetonitrile ; 5 min, 20 - 25 °C
1.2 Reagents: Water Solvents: Dichloromethane ; 10 - 15 min, 20 - 25 °C
1.2 Reagents: Water Solvents: Dichloromethane ; 10 - 15 min, 20 - 25 °C
Reference
- Activator free, expeditious and eco-friendly chlorination of activated arenes by N-chloro-N-(phenylsulfonyl)benzene sulfonamide (NCBSI)Misal, Balu; Palav, Amey; Ganwir, Prerna; Chaturbhuj, Ganesh, Tetrahedron Letters, 2021, 63,
Production Method 5
Reaction Conditions
1.1 Reagents: Sodium carbonate Catalysts: Tetrakis(triphenylphosphine)palladium Solvents: 1,2-Dimethoxyethane , Water ; overnight, 95 °C
Reference
- ERβ Ligands. Part 1: The discovery of ERβ selective ligands which embrace the 4-hydroxy-biphenyl templateEdsall, Richard J.; Harris, Heather A.; Manas, Eric S.; Mewshaw, Richard E., Bioorganic & Medicinal Chemistry, 2003, 11(16), 3457-3474
Production Method 6
Reaction Conditions
1.1 Reagents: 1,3-Dichloro-5,5-dimethylhydantoin Catalysts: 2-Propanamine, N-(1-methylethyl)-, hydrochloride (1:1) Solvents: Toluene ; 4 h, 0 °C
1.2 Reagents: Sodium sulfite Solvents: Water
1.2 Reagents: Sodium sulfite Solvents: Water
Reference
- Ammonium Salt-Catalyzed Highly Practical Ortho-Selective Monohalogenation and Phenylselenation of Phenols: Scope and ApplicationsXiong, Xiaodong ; Yeung, Ying-Yeung, ACS Catalysis, 2018, 8(5), 4033-4043
Production Method 7
Reaction Conditions
1.1 Reagents: Chlorosuccinimide , Aluminum chloride Solvents: Dichloromethane ; rt
Reference
- Multisubstituted benzo[b]furans through a copper- and/or palladium-catalyzed assembly and functionalization processArcadi, Antonio; Blesi, Federico; Cacchi, Sandro; Fabrizi, Giancarlo; Goggiamani, Antonella; et al, Tetrahedron, 2013, 69(7), 1857-1871
Production Method 8
Reaction Conditions
1.1 Reagents: Chlorosuccinimide Catalysts: Zirconium chloride (ZrCl4) Solvents: Dichloromethane ; -78 °C; 6 h, rt
1.2 Reagents: Sodium bicarbonate Solvents: Water
1.2 Reagents: Sodium bicarbonate Solvents: Water
Reference
- Modular Synthesis of Indoles from Imines and o-Dihaloarenes or o-Chlorosulfonates by a Pd-Catalyzed Cascade ProcessBarluenga, Jose; Jimenez-Aquino, Agustin; Aznar, Fernando; Valdes, Carlos, Journal of the American Chemical Society, 2009, 131(11), 4031-4041
Production Method 9
Reaction Conditions
1.1 Reagents: Methyl triflate Solvents: Toluene ; 2 h, 100 °C
1.2 Reagents: Sodium Solvents: Methanol ; 30 min, rt → 80 °C
1.2 Reagents: Sodium Solvents: Methanol ; 30 min, rt → 80 °C
Reference
- Regioselective C-H chlorination: towards the sequential difunctionalization of phenol derivatives and late-stage chlorination of bioactive compoundsGao, Chao; Li, Hongchen; Liu, Miaochang; Ding, Jinchang; Huang, Xiaobo; et al, RSC Advances, 2017, 7(74), 46636-46643
Production Method 10
Reaction Conditions
1.1 Reagents: Potassium carbonate Catalysts: Tetrakis(triphenylphosphine)palladium Solvents: Toluene , Water ; rt
Reference
- Carbazole derivative organic light-emitting compound, ink composition for organic light-emitting diode, World Intellectual Property Organization, , ,
Production Method 11
Production Method 12
Reaction Conditions
Reference
- Direct Spectroscopic Observation of Closed-Shell Singlet, Open-Shell Singlet, and Triplet p-Biphenylyloxenium IonLi, Ming-De; Hanway, Patrick J.; Albright, Toshia R.; Winter, Arthur H.; Phillips, David Lee, Journal of the American Chemical Society, 2014, 136(35), 12364-12370
Production Method 13
Reaction Conditions
Reference
- Palladium-catalyzed phenylation of chloroarenes by sodium tetraphenylborate in aqueous mediaBykov, V. V.; Bumagin, N. A.; Beletskaya, I. P., Doklady Akademii Nauk, 1995, 340(6), 775-8
3-chloro-1,1'-biphenyl-4-ol Raw materials
- Phenylboronic acid
- 4-Bromo-2-chlorophenol
- 2,5-Cyclohexadien-1-one, 4-methoxy-4-phenyl-
- Sodium Tetraphenylboroate
- 4-Hydroxybiphenyl
3-chloro-1,1'-biphenyl-4-ol Preparation Products
3-chloro-1,1'-biphenyl-4-ol Related Literature
-
Yi Cao,Yujiao Xiahou,Lixiang Xing,Xiang Zhang,Hong Li,ChenShou Wu,Haibing Xia Nanoscale, 2020,12, 20456-20466
-
Yukiya Kitayama Polym. Chem., 2014,5, 2784-2792
-
Ziyang Deng,Changwei Chen,Sunliang Cui RSC Adv., 2016,6, 93753-93755
-
Andreas Nenning,Manuel Holzmann,Jürgen Fleig,Alexander K. Opitz Mater. Adv., 2021,2, 5422-5431
-
Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
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