191162-40-0

191162-40-0 - Names and Identifiers

Name	1-METHYL-1H-INDOLE-2-BORONIC ACID
Synonyms	AKOS BRN-0885 N-METHYLINDOLE-2-BORONIC ACID N-METHYL-2-INDOLEBORONIC ACID 1-Methyl-1H-indole-2-boronic acid 1-METHYL-1H-INDOLE-2-BORONIC ACID (1-METHYL-1H-IND-2-YL)BORONIC ACID (1-METHYL-1H-INDOL-2-YL)BORONIC ACID 1-METHYL-1H-INDOLE-2-BORONIC ACID 2,2-DIMETHYL PROPANE DIOL-1,3-CYCLIC ESTER
CAS	191162-40-0
InChI	InChI=1/C9H10BNO2/c1-11-8-5-3-2-4-7(8)6-9(11)10(12)13/h2-6,12-13H,1H3

191162-40-0 - Physico-chemical Properties

Molecular Formula	C9H10BNO2
Molar Mass	174.99
Density	1.16
Melting Point	108-112
Boling Point	402.6±37.0 °C(Predicted)
Flash Point	197.269°C
Vapor Presure	0mmHg at 25°C
pKa	9.39±0.30(Predicted)
Storage Condition	Inert atmosphere,Store in freezer, under -20°C
Refractive Index	1.571
Physical and Chemical Properties	Storage Conditions: Keep Cold

191162-40-0 - Risk and Safety

Hazard Symbols	Xi - Irritant
Risk Codes	R37/38 - Irritating to respiratory system and skin. R41 - Risk of serious damage to eyes
Safety Description	S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S39 - Wear eye / face protection.
Hazard Note	Irritant/Keep Cold

191162-40-0 - Introduction

Ithorium ACID, also known as 2-indole methyl boronic ACID or IMes-B(OH)2, is an Organoboron compound. Its chemical formula is C9H10BNO2 and its molecular weight is 178.99.

The Nature of ACID:
-Appearance is white solid crystal.
-Stable at room temperature, but avoid exposure to humid air, because it is easy to absorb moisture.
-It has good solubility in solvents such as ethanol, and can also be dissolved in hydrofluoric acid, and can be used for addition reactions.
-has good thermal stability.
-Can be further converted to the corresponding boron Ester compound under acidic conditions.

usages of ACID:
-As a catalyst in organic synthesis, it plays an important role in the reduction reaction of carbonyl compounds.
-In the cross-coupling reaction, the compound can be used as a source of Pd (Palladium) ligands to promote the coupling between different functional groups.
-Used to prepare other organic boron compounds, such as ACID ester, etc.

preparation method of ACID:
It is usually prepared by the reaction of N-methylindole and Tris (benzyloxy) borate under basic conditions.

ACID safety information:
Take proper safety precautions during operation to avoid skin and eye contact. During handling and storage, contact with moisture should be avoided to avoid hazardous substances.

Last Update：2024-04-10 22:29:15