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1-Benzothiophen-2-ylboronic acid

Names

[ CAS No. ]:
98437-23-1

[ Name ]:
1-Benzothiophen-2-ylboronic acid

[Synonym ]:
1-Benzothiophen-2-ylboronic acid
MFCD01075674
benzo(b)thiophene-2-ylboronic acid
benzo(b)thiophene-2-boronic acid
Boronic acid, B-benzo[b]thien-2-yl-

Chemical & Physical Properties

[ Density]:
1.4±0.1 g/cm3

[ Boiling Point ]:
390.2±34.0 °C at 760 mmHg

[ Melting Point ]:
254-256 °C

[ Molecular Formula ]:
C8H7BO2S

[ Molecular Weight ]:
178.016

[ Flash Point ]:
189.8±25.7 °C

[ Exact Mass ]:
178.025986

[ PSA ]:
68.70000

[ LogP ]:
3.75

[ Vapour Pressure ]:
0.0±0.9 mmHg at 25°C

[ Index of Refraction ]:
1.669

[ Storage condition ]:
0-6°C

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S37/39-S26

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2934999090

Synthetic Route

Customs

[ HS Code ]: 2934999090

[ Summary ]:
2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Discovery of boronic acids as novel and potent inhibitors of fatty acid amide hydrolase.

J. Med. Chem. 51 , 7057-7060, (2008)

A series of commercial phenyl-, heteroaryl-, alkyl-, and alkenylboronic acids were evaluated for their FAAH and MGL inhibitory activities. The compounds were generally selective for FAAH, with IC50 in...

Synthesis and evaluation of 3-(dihydroxyboryl)benzoic acids as D,D-carboxypeptidase R39 inhibitors.

J. Med. Chem. 52 , 6097-106, (2009)

Penicillin binding proteins (PBPs) catalyze steps in the biosynthesis of bacterial cell walls and are the targets for the beta-lactam antibiotics. Non-beta-lactam based antibiotics that target PBPs ar...

Optimizing cell permeation of an antibiotic resistance inhibitor for improved efficacy.

J. Med. Chem. 50 , 5644, (2007)

Benzo[b]thiophene-2-ylboronic acid, 1, is a 27 nM inhibitor of the class C beta-lactamase AmpC and potentiates the activity of beta-lactam antibiotics in bacteria that express this and related enzymes...


More Articles


Related Compounds

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