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913642-07-6

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913642-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 913642-07-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,6,4 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 913642-07:
(8*9)+(7*1)+(6*3)+(5*6)+(4*4)+(3*2)+(2*0)+(1*7)=156
156 % 10 = 6
So 913642-07-6 is a valid CAS Registry Number.

913642-07-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-N-ethyl-5-nitropyridin-4-amine

1.2 Other means of identification

Product number -
Other names 2-bromo-N-ethyl-5-nitro-4-pyridinamine

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:913642-07-6 SDS

913642-07-6Relevant articles and documents

Aminofurazans as potent inhibitors of AKT kinase

Rouse, Meagan B.,Seefeld, Mark A.,Leber, Jack D.,McNulty, Kenneth C.,Sun, Lihui,Miller, William H.,Zhang, ShuYun,Minthorn, Elisabeth A.,Concha, Nestor O.,Choudhry, Anthony E.,Schaber, Michael D.,Heerding, Dirk A.

scheme or table, p. 1508 - 1511 (2009/11/30)

AKT inhibitors containing an imidazopyridine aminofurazan scaffold have been optimized. We have previously disclosed identification of the AKT inhibitor GSK690693, which has been evaluated in clinical trials in cancer patients. Herein we describe recent efforts focusing on investigating a distinct region of this scaffold that have afforded compounds (30 and 32) with comparable activity profiles to that of GSK690693.

INHIBITORS OF AKT ACTIVITY

-

, (2008/06/13)

Invented are novel 1 H-imidazo[4,5-c]pyridin-2-yl compounds, the use of such compounds as inhibitors of protein kinase B activity and in the treatment of cancer and arthritis.

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