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1187968-75-7

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1187968-75-7 Usage

Uses

6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazol-3-amine can be used as reactant/reagent along with other materials for preparation of phosphoinositide 3-kinase inhibition, and pharmacokinetics of pyrrolopyrimidines.

Check Digit Verification of cas no

The CAS Registry Mumber 1187968-75-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,7,9,6 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1187968-75:
(9*1)+(8*1)+(7*8)+(6*7)+(5*9)+(4*6)+(3*8)+(2*7)+(1*5)=227
227 % 10 = 7
So 1187968-75-7 is a valid CAS Registry Number.

1187968-75-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazol-3-amine

1.2 Other means of identification

Product number -
Other names -

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:1187968-75-7 SDS

1187968-75-7Downstream Products

1187968-75-7Relevant articles and documents

An amino-indazole scaffold with spectrum selective kinase inhibition of FLT3, PDGFRα and kit

Deng, Xianming,Zhou, Wenjun,Weisberg, Ellen,Wang, Jinhua,Zhang, Jianming,Sasaki, Takaaki,Nelson, Erik,Griffin, James D.,Jaenne, Pasi A.,Gray, Nathanael S.

, p. 4579 - 4584 (2012/08/07)

Here we describe the synthesis and characterization of a number of 3-amino-1H-indazol-6-yl-benzamides that were designed to target the 'DFG-out' conformation of the kinase activation loop. Several compounds such as 4 and 11 exhibit single-digit nanomolar EC50s against FLT3, c-Kit and the gatekeeper T674M mutant of PDGFRα.

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