- Cp*Rh(III)/boron hybrid catalysis for directed C-H addition to β-substituted α,β-unsaturated carboxylic acidsBy Tanaka, Ryo et al, Chemical Communications (Cambridge, 2022, 58(1), 76-79
Cas no 98061-20-2 (Benzoic acid, 3-(2-pyridinyl)-, methyl ester)
98061-20-2 structure
Product Name:Benzoic acid, 3-(2-pyridinyl)-, methyl ester
CAS No:98061-20-2
MF:C13H11NO2
MW:213.231943368912
MDL:MFCD06801883
CID:1083076
Update Time:2025-04-20
Benzoic acid, 3-(2-pyridinyl)-, methyl ester Chemical and Physical Properties
Names and Identifiers
-
- Methyl 3-(pyridin-2-yl)benzoate
- Methyl 3-(2-pyridinyl)benzoate
- 3-(Pyridin-2-yl)benzoic acid methyl ester
- Benzoic acid, 3-(2-pyridinyl)-, methyl ester
-
- MDL： MFCD06801883
- Inchi： 1S/C13H11NO2/c1-16-13(15)11-6-4-5-10(9-11)12-7-2-3-8-14-12/h2-9H,1H3
- InChI Key： WSFNTSUFRZCBNQ-UHFFFAOYSA-N
- SMILES： O(C)C(C1=CC=CC(C2C=CC=CN=2)=C1)=O
Benzoic acid, 3-(2-pyridinyl)-, methyl ester Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A029195171-5g |
Methyl 3-(pyridin-2-yl)benzoate |
98061-20-2 | 95% | 5g |
$515.90 | 2023-08-31 | |
| Alichem | A029195171-10g |
Methyl 3-(pyridin-2-yl)benzoate |
98061-20-2 | 95% | 10g |
$670.00 | 2023-08-31 | |
| Alichem | A029195171-25g |
Methyl 3-(pyridin-2-yl)benzoate |
98061-20-2 | 95% | 25g |
$1323.92 | 2023-08-31 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | X56885-100mg |
Methyl 3-(pyridin-2-yl)benzoate |
98061-20-2 | 95% | 100mg |
￥191.0 | 2024-07-18 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | X56885-5g |
Methyl 3-(pyridin-2-yl)benzoate |
98061-20-2 | 95% | 5g |
￥3241.0 | 2024-07-18 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | X56885-250mg |
Methyl 3-(pyridin-2-yl)benzoate |
98061-20-2 | 95% | 250mg |
￥333.0 | 2024-07-18 | |
| SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd. | X56885-1g |
Methyl 3-(pyridin-2-yl)benzoate |
98061-20-2 | 95% | 1g |
￥832.0 | 2024-07-18 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-OQ936-200mg |
Benzoic acid, 3-(2-pyridinyl)-, methyl ester |
98061-20-2 | 95+% | 200mg |
312.0CNY | 2021-07-10 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-OQ936-50mg |
Benzoic acid, 3-(2-pyridinyl)-, methyl ester |
98061-20-2 | 95+% | 50mg |
124.0CNY | 2021-07-10 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | B-OQ936-1g |
Benzoic acid, 3-(2-pyridinyl)-, methyl ester |
98061-20-2 | 95+% | 1g |
1092.0CNY | 2021-07-10 |
Benzoic acid, 3-(2-pyridinyl)-, methyl ester Production Method
Production Method 1
Reaction Conditions
1.1R:K3PO4, C:Pd(OAc)2, C:657408-07-6, S:PhMe, 100°C
Reference
Production Method 2
Reaction Conditions
1.1R:Disodium carbonate, C:Pd(PPh3)4, S:H2O, 18 h, reflux
Reference
- Three-Component Couplings among Heteroarenes, Difluorocyclopropenes, and Water via C-H ActivationBy Liu, Xuexin et al, Organic Letters, 2021, 23(17), 6831-6835
Production Method 3
Reaction Conditions
1.1R:Disodium carbonate, C:Pd(PPh3)4, S:H2O, S:MeOH, S:PhMe, 24 h, 80°C
Reference
- N-heterocyclic carbene enabled rhodium-catalyzed ortho C(sp2)-H borylation at room temperatureBy Zhong, Lei et al, Tetrahedron, 2019, 75(17), 2547-2552
Production Method 4
Reaction Conditions
1.1C:72287-26-4, S:H2O, S:Dioxane, 30 min, 120°C
Reference
- Sterol 14α-Demethylase Structure-Based Design of VNI ((R)-N-(1-(2,4-Dichlorophenyl)-2-(1H-imidazol-1-yl)ethyl)-4-(5-phenyl-1,3,4-oxadiazol-2-yl)benzamide)) Derivatives To Target Fungal Infections: Synthesis, Biological Evaluation, and Crystallographic AnalysisBy Friggeri, Laura et al, Journal of Medicinal Chemistry, 2018, 61(13), 5679-5691
Production Method 5
Reaction Conditions
1.1R:K2CO3, C:72287-26-4, S:H2O, S:Dioxane, 30 min, 120°C
Reference
- Structure and Property Guided Design in the Identification of PRMT5 Tool Compound EPZ015666By Duncan, Kenneth W. et al, ACS Medicinal Chemistry Letters, 2016, 7(2), 162-166
Production Method 6
Reaction Conditions
1.1R:i-PrMgCl, S:THF, 0°C; 0°C → rt; 4 h, rt
1.2R:ZnCl2, S:THF, 0°C; 0°C → rt; 2 h, rt
1.3R:Dioxane, rt
1.4C:1445085-55-1, S:THF, 16 h, rt
1.2R:ZnCl2, S:THF, 0°C; 0°C → rt; 2 h, rt
1.3R:Dioxane, rt
1.4C:1445085-55-1, S:THF, 16 h, rt
Reference
- Synthesis of Solid 2-Pyridylzinc Reagents and Their Application in Negishi ReactionsBy Colombe, James R. et al, Organic Letters, 2013, 15(22), 5754-5757
Production Method 7
Reaction Conditions
1.1
Reference
- Ruthenium-Catalyzed Monoselective C-H Methylation and d3-Methylation of ArenesBy Hogg, Ashley et al, JACS Au, 2022, 2(11), 2529-2538
Production Method 8
Reaction Conditions
1.1
2.1
3.1R:K2CO3, C:1188-21-2, S:MeCN, 24 h, 120°C
4.1R:NaOH, R:I2, R:t-BuOOH, S:H2O, 70°C
4.2
2.1
3.1R:K2CO3, C:1188-21-2, S:MeCN, 24 h, 120°C
4.1R:NaOH, R:I2, R:t-BuOOH, S:H2O, 70°C
4.2
Reference
- Ruthenium-Catalyzed meta-Selective CAr-H Bond Formylation of ArenesBy Jia, Chunqi et al, Journal of Organic Chemistry, 2020, 85(6), 4536-4542
Production Method 9
Reaction Conditions
1.1R:K3PO4, C:Pd(OAc)2, S:H2O, S:Me2CHOH, overnight, 80°C
Reference
- Pentamethylcyclopentadienyl rhodium(III)-chiral disulfonate hybrid catalysis for enantioselective C-H bond functionalizationBy Satake, Shun et al, Nature Catalysis, 2018, 1(8), 585-591
Production Method 10
Reaction Conditions
1.1R:Disodium carbonate, C:Pd(PPh3)4, S:H2O, S:EtOH, 12 h, reflux
Reference
- Enabling Catalytic Arene C-H Amidomethylation via Bis(tosylamido)methane as a Sustainable Formaldimine ReleaserBy Li, Zhong-Yuan et al, Organic Letters, 2019, 21(10), 3735-3740
Production Method 11
Reaction Conditions
1.1R:t-BuOCl, R:K2CO3, R:O2, 20 h, 60°C
Reference
- Transition-Metal-Free Decarboxylative Arylation of 2-Picolinic Acids with Arenes under Air ConditionsBy Zhang, Xitao et al, Organic Letters, 2018, 20(22), 7095-7099
Production Method 12
Reaction Conditions
1.1C:RuCl3 ?xH2O, S:Dioxane, S:MeOH, 16 h, 85°C
Reference
- Ruthenium-Catalyzed meta-CarboxylationBy Barlow, Helen L. et al, Organic Letters, 2017, 19(24), 6662-6665
Production Method 13
Reaction Conditions
1.1
Reference
- Highly ortho-selective trifluoromethylthiolation reactions using a ligand exchange strategyBy Yin, Weiyu et al, Advanced Synthesis & Catalysis, 2014, 356(14-15), 2998-3006
Benzoic acid, 3-(2-pyridinyl)-, methyl ester Raw materials
- Picolinic acid
- 2-Phenylpyridine
- 2-Bromopyridine
- Methyl 3-chlorobenzoate
- [3-(methoxycarbonyl)phenyl]boronic acid
- Methyl benzoate
- Dichloro(p-cymene)ruthenium(II) dimer
- Potassium Acetate
Benzoic acid, 3-(2-pyridinyl)-, methyl ester Preparation Products
Benzoic acid, 3-(2-pyridinyl)-, methyl ester Related Literature
-
M. Sheykhan,S. Khani,S. Shaabanzadeh,M. Joafshan Green Chem., 2017,19, 5940-5948
-
Shivani Sharma,Chia-Ming Wu,Ranjit T. Koodali,N. Rajesh RSC Adv., 2016,6, 26668-26678
-
Cheng Fang,Jinjian Wu,Zahra Sobhani,Md. Al Amin,Youhong Tang Anal. Methods, 2019,11, 163-170
98061-20-2 (Benzoic acid, 3-(2-pyridinyl)-, methyl ester) Related Products
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- 92199-59-2(4-Pyridinecarboxylic acid, 2-phenyl-, ethyl ester)
- 4634-14-4(4-Pyridinecarboxylicacid, 2-phenyl-, methyl ester)
- 4634-13-3(3-Pyridinecarboxylicacid, 6-phenyl-, methyl ester)
- 834884-66-1(Methyl 4-(5-formylpyridin-2-yl)benzoate)
- 579476-62-3([2,4'-Bipyridine]-4-carboxylic acid, 2'-methyl-, methyl ester)
- 834884-81-0(METHYL 4-(6-FORMYLPYRIDIN-2-YL)BENZOATE&)
- 834884-82-1(Methyl 3-(6-formylpyridin-2-yl)benzoate)
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