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2-Methoxycarbonylphenylboronic acid

CAS No.
374538-03-1
Chemical Name:
2-Methoxycarbonylphenylboronic acid
Synonyms
1-Methyl 2-boronobenzoate;Bm199;METHYL 2-BORONOBENZOATE;Chemical Formula: C18H19BO6;2-(Methoxycarbonyl)Phenylboron;2-Carbomethoxybenzeneboronicacid;2-Methoxycarbonylphenylboronicaci;2-(methoxylated)benzylboronic acid;2-METHOXYCARBONYLPHENYLBORONIC ACID;Benzoicacid,2-borono-,1-methylester
CBNumber:
CB7349102
Molecular Formula:
C8H9BO4
Molecular Weight:
179.97
MDL Number:
MFCD02179452
MOL File:
374538-03-1.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 05:27:32
Product description Number Pack Size Price
2-Methoxycarbonylphenylboronic acid ≥95.0% 683809 5g $115
2-Methoxycarbonylphenylboronic acid ≥95.0% 683809 1g $32
2-(Methoxycarbonyl)phenylboronic Acid (contains varying amounts of Anhydride) M1905 1g $31
2-(Methoxycarbonyl)phenylboronic Acid (contains varying amounts of Anhydride) M1905 5g $77
2-(METHOXYCARBONYL)PHENYLBORONIC ACID 95% 64160 1G $12
More product size

2-Methoxycarbonylphenylboronic acid Properties

Melting point 90-96°C
Boiling point 359.0±44.0 °C(Predicted)
Density 1.25±0.1 g/cm3(Predicted)
storage temp. Inert atmosphere,Store in freezer, under -20°C
solubility soluble in Methanol
pka 8.19±0.58(Predicted)
form Crystalline Powder
color White
BRN 8313459
InChI 1S/C8H9BO4/c1-13-8(10)6-4-2-3-5-7(6)9(11)12/h2-5,11-12H,1H3
InChIKey ODAXNYMENLFYMY-UHFFFAOYSA-N
SMILES COC(=O)c1ccccc1B(O)O
CAS DataBase Reference 374538-03-1(CAS DataBase Reference)
UNSPSC Code 12352103
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a
PPE Eyeshields, Gloves, type N95 (US)
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36/37/39
WGK Germany  3
TSCA  No
HazardClass  IRRITANT
HS Code  29163990
Storage Class 11 - Combustible Solids
NFPA 704
1
2 0

2-Methoxycarbonylphenylboronic acid price More Price(62)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 683809 2-Methoxycarbonylphenylboronic acid ≥95.0% 374538-03-1 5g $115 2026-04-30 Buy
Sigma-Aldrich 683809 2-Methoxycarbonylphenylboronic acid ≥95.0% 374538-03-1 1g $32 2023-06-20 Buy
TCI Chemical M1905 2-(Methoxycarbonyl)phenylboronic Acid (contains varying amounts of Anhydride) 374538-03-1 1g $31 2026-04-30 Buy
TCI Chemical M1905 2-(Methoxycarbonyl)phenylboronic Acid (contains varying amounts of Anhydride) 374538-03-1 5g $77 2026-04-30 Buy
AstaTech 64160 2-(METHOXYCARBONYL)PHENYLBORONIC ACID 95% 374538-03-1 1G $12 2026-04-30 Buy
Product number Packaging Price Buy
683809 5g $115 Buy
683809 1g $32 Buy
M1905 1g $31 Buy
M1905 5g $77 Buy
64160 1G $12 Buy

2-Methoxycarbonylphenylboronic acid Chemical Properties,Uses,Production

Chemical Properties

White to brown powder

Uses

2-Methoxycarbonylphenylboronic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

General Description

May contain varying amounts of anhydride

Synthesis

Methanol

67-56-1

2-Carboxyphenylboronic acid

149105-19-1

2-Methoxycarbonylphenylboronic acid

374538-03-1

In a 20 L autoclave, 7.5 g of anhydrous methanol and 1.66 Kg (10 mol) of 2-carboxyphenylboronic acid were added and stirring was initiated to mix the reactants. The temperature of the reaction kettle was slowly raised to 40 °C and maintained in the range of 40 to 55 °C. Subsequently, thionyl chloride (1.31 Kg, 11 mol) was slowly added dropwise to the reaction kettle, and after the dropwise addition was completed, the temperature was raised to reflux condition and the reaction was continued for 2-3 hours. The completion of the reaction was confirmed by thin layer chromatography (TLC, unfolding agent ratio of n-heptane: ethyl acetate = 2:1). Upon completion of the reaction, the reaction solution was cooled and subsequently subjected to reduced pressure distillation to remove the solvent. The residue was cooled to -10°C to 10°C and stirred at this temperature for 1 hour. Next, the drying process was stopped by filtration under reduced pressure at 80 °C until no impurities were confirmed to be present by hydrogen nuclear magnetic resonance (HNMR, observing the peak at 3.21 ppm with DMSO-d6 as solvent). Finally, the mixture was stirred at room temperature, filtered and dried at room temperature to give 1.74 Kg of the white solid product 2-(methoxycarbonyl)phenylboronic acid in 96.7% yield with 19.8% water and 140.5% Karl Fischer moisture.

References

[1] Patent: CN106188117, 2016, A. Location in patent: Paragraph 0014

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View Lastest Price from 2-Methoxycarbonylphenylboronic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2-Methoxycarbonylphenylboronic acid pictures 2026-06-01 2-Methoxycarbonylphenylboronic acid
374538-03-1
1kg 99%min 20tons HANGZHOU HAILAN CHEMICAL CO.,LTD.
2-Methoxycarbonylphenylboronic acid pictures 2025-05-23 2-Methoxycarbonylphenylboronic acid
374538-03-1
$10.00 1kg 99% 20 ton Hebei Zhuanglai Chemical Trading Co Ltd
2-Methoxycarbonylphenylboronic acid pictures 2021-07-13 2-Methoxycarbonylphenylboronic acid
374538-03-1
$10.00-15.00 1KG 99%+ HPLC Zhuozhou Wenxi import and Export Co., Ltd
METHYL 2-BORONOBENZOATE 2-(METHOXYCARBONYL)BENZENEBORONIC ACID 2-METHOXYCARBONYLPHENYLBORONIC ACID O-(METHOXYCARBONYL)PHENYLBORONIC ACID Benzoic acid, 2-borono-, 1-methyl ester (9CI) 2-Carbomethoxybenzeneboronicacid 2-(Methoxycarbonyl)Phenylboron 2-(Methoxycarbonyl)phenylboronic Acid (contains varying amounts of Anhydride) 2-Methoxycarbonylphenylboronic acid ,97% Bm199 2-Methoxycarbonylphenylboronic acid (2-Methoxycarbonylphenyl)boronic acid Chemical Formula: C18H19BO6 Benzoic acid, 2-borono-, methyl ester Benzoicacid,2-borono-,1-methylester 2-Methoxycarbonylphenylboronicaci (2-(methoxycarbamoyl)phenyl)boronic acid 2-(methoxylated)benzylboronic acid 1-Methyl 2-boronobenzoate 374538-03-1 CH3O2CC6H4BOH2 C8H9O4B BORONIC ACID Aryl Boronic Acids Boronic Acids and Derivatives Chemical Synthesis Monosubstituted Aryl Boronic Acids Organometallic Reagents Boronate Ester Boronic Acid Potassium Trifluoroborate blocks BoronicAcids Carboxes Boronic acids BORONICACID B (Classes of Boron Compounds) Aryl Boronic Acids Boronic Acids and Derivatives