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100510-65-4

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100510-65-4 Usage

Uses

6-Amino-3,3-dimethylindolin-2-one is a versatile reactant used in the preparation of selective and potent aminoisoquinoline derivatives as inhibitors of mutant B-Raf pathway. It is also used in the synthesis of pentacyclic aurora kinase inhibitors.

Check Digit Verification of cas no

The CAS Registry Mumber 100510-65-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,5,1 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100510-65:
(8*1)+(7*0)+(6*0)+(5*5)+(4*1)+(3*0)+(2*6)+(1*5)=54
54 % 10 = 4
So 100510-65-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2O/c1-10(2)7-4-3-6(11)5-8(7)12-9(10)13/h3-5H,11H2,1-2H3,(H,12,13)

100510-65-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Amino-3,3-dimethylindolin-2-one

1.2 Other means of identification

Product number -
Other names 6-amino-3,3-dimethyl-1H-indol-2-one

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:100510-65-4 SDS

100510-65-4Relevant articles and documents

Pyrazolopyrimidine compounds and preparation method thereof, and applications in preparation of anti-cancer drugs

-

, (2020/04/17)

The invention provides a class of pyrazolopyrimidine compounds represented by a formula (I) or pharmaceutically acceptable salts thereof, and a preparation method thereof, and applications of the pyrazolopyrimidine compounds or the pharmaceutically accept

3,3-Dimethyl-1H-pyrrolo[3,2-g]quinolin-2(3H)-one derivatives as novel Raf kinase inhibitors

Li, Yanyang,Shi, Xiangfei,Xie, Ning,Zhao, Yanjin,Li, Shuxin

, p. 367 - 370 (2013/06/05)

A series of quinoline derivatives were designed and synthesized as tyrosine kinase inhibitors. Exploration of the structure-activity relationships resulted in compounds that are potent in vitro. In addition, compound 10f was found to be a potent and selec

HETEROCYCLE-SUBSTITUTED CYCLIC UREA DERIVATIVES, PREPARATION THEREOF AND PHARMACEUTICAL USE THEREOF AS KINASE INHIBITORS

-

Page/Page column 105, (2010/02/15)

The invention relates to the novel products of formula (I), in which V represents a heterocyclic radical, as protein kinases inhibitors.

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