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1197171-76-8

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1197171-76-8 Usage

General Description

N-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide is a compound with the chemical formula C16H21BO3N. It is an organoboron compound that contains a benzamide group and a boron atom attached to a dioxaborolane ring. This chemical is used in organic synthesis as a reagent for the introduction of boron into organic molecules. It is also used in catalysis and as a building block for the preparation of various biologically active compounds. N-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide plays a crucial role in the development of new materials and pharmaceuticals.

Check Digit Verification of cas no

The CAS Registry Mumber 1197171-76-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,7,1,7 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1197171-76:
(9*1)+(8*1)+(7*9)+(6*7)+(5*1)+(4*7)+(3*1)+(2*7)+(1*6)=178
178 % 10 = 8
So 1197171-76-8 is a valid CAS Registry Number.

1197171-76-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

1.2 Other means of identification

Product number -
Other names X1655

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1197171-76-8 SDS

1197171-76-8Relevant articles and documents

Highly regioselective Ru(II)-catalyzed [3+2] spiroannulation of 1-aryl-2-naphthols with alkynes via a double directing group strategy

Hao, Jiamao,Ge, Yicong,Yang, Liuqing,Wang, Jing,Luan, Xinjun

, (2021)

A highly regioselective Ru(II)-catalyzed [3+2] spiroannulation of 1-aryl-2-naphthols with internal alkynes was developed by using a novel double directing group strategy. This method was compatible with many functional groups, thus affording a variety of sterically congested spirocyclic molecules in high yields.

HETEROCYCLIC COMPOUNDS AS MTOR INHIBITORS

-

Page/Page column 36-38, (2021/07/02)

The present disclosure describes novel heterocyclic mTOR inhibitors and methods for preparing them. The pharmaceutical compositions comprising such mTOR inhibitors and methods of using them for treating cancer, infectious diseases, and other mTOR associated disorders are also described.

NURR1 RECEPTOR MODULATORS

-

, (2020/09/08)

Described herein, inter alia, are Nurr1 receptor modulators and uses thereof. In an aspect is provided a method for treating a disease associated with dysregulation and/or degeneration of dopaminergic neurons in the central nervous system of a subject in need thereof, the method including administering to the subject in need thereof a therapeutically effective amount of a compound described herein.

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