351422-73-6 3-Aminocarbonylphenylboronic Acid

351422-73-6 3-Aminocarbonylphenylboronic Acid

3-Aminocarbonylphenylboronic acid Basic information 3-Aminocarbonylphenylboronic acid Chemical Properties Safety Information 3-Aminocarbonylphenylboronic acid Usage And Synthesis
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Product Details

3-Aminocarbonylphenylboronic acid Basic information


Product Name:

3-Aminocarbonylphenylboronic acid

Synonyms:

BENZAMIDE-3-BORONIC ACID;3-CARBAMOYLPHENYLBORONIC ACID;3-CARBAMOYLPHENYLBORONIC ACID,    3-BORONOBENZAMIDE;3-CARBOXAMIDEPHENYLBORONIC ACID;3-(AMINOCARBONYL)BENZENEBORONIC    ACID;3-AMINOCARBONYLPHENYLBORONIC ACID;3-AMINOCARBONYLPENYLBORONIC ACID;3-Aminocarbonyiphenylboronic acid

CAS:

351422-73-6

MF:

C7H8BNO3

MW:

164.95

EINECS:


Product Categories:

blocks;BoronicAcids;Carboxes;Boronic acids;Heterocyclic Compounds;Amide;Aryl;Organoborons;Boronic acid;Aryl Boronic Acids;Boronic Acids and Derivatives;Chemical Synthesis;Monosubstituted Aryl Boronic Acids;Organometallic Reagents;Boronate Ester;Potassium Trifluoroborate

Mol File:

351422-73-6.mol

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3-Aminocarbonylphenylboronic acid Chemical Properties


Melting point 

232-235°C

storage temp. 

Keep Cold

form 

Solid

color 

White to off-white

Density:

1.32 g/cm3

Melting    Point:

232-235ºC

Boiling    Point:

408.1ºC at 760 mmHg

Flash    Point:

200.6ºC

Refractive Index:

1.585

StorageCondition:

Keep Cold

CAS DataBaseReference

351422-73-6(CAS DataBase Reference)



Safety Information


Hazard Codes 

Xi,Xn

Risk Statements 

22-36/37/38-20/21/22

Safety Statements 

26-36-24/25

Hazard Note 

Corrosive

HazardClass 

IRRITANT

HS Code 

29310095



3-Aminocarbonylphenylboronic acid Usage And Synthesis

Chemical Properties

White to brown solid

Uses

Reactant involved in the synthesis of a variety of inhibitors including:• ;Orally active phosphodiesterase 10A inhibitors1• ;Pyrimidine derivatives as TpI2 kinase inhibitors2• ;Peptidomimetic inhibitors of STAT3 protein3Reactant involved in:• ;Oxidative    cross-coupling with mercaptoacetylenes4• ;Trifluoromethylation via a Collidine trifluoromethylating agent5• ;Suzuki cross-coupling reactions6

Uses

suzuki reaction

Intermediate as

778270-11-4 GNF-2
     

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Synthesis route

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