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886372-76-5

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886372-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 886372-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,3,7 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 886372-76:
(8*8)+(7*8)+(6*6)+(5*3)+(4*7)+(3*2)+(2*7)+(1*6)=225
225 % 10 = 5
So 886372-76-5 is a valid CAS Registry Number.

886372-76-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-bromo-2-ethoxy-3-nitropyridine

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:886372-76-5 SDS

886372-76-5Relevant articles and documents

TYK2 INHIBITORS AND USES THEREOF

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Paragraph 00556, (2020/06/19)

The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of TYK2, and the treatment of TYK2-mediated disorders.

COMPOUNDS AND COMPOSITIONS AS RAF KINASE INHIBITORS

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Paragraph 00143, (2016/04/20)

The present invention provides compounds of Formula (I) and (II) as described herein, and salts thereof, and therapeutic uses of these compounds for treatment of disorders associated with Raf kinase activity. The invention further provides pharmaceutical compositions comprising these compounds, and compositions comprising these compounds and a therapeutic co-agent.

4-CARBOXAMIDE INDAZOLE DERIVATIVES USEFUL AS INHIBITORS OF P13-KINASES

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Page/Page column 132-133, (2009/12/28)

The invention is directed to certain novel compounds. Specifically, the invention is directed to compounds of formula (I) and salts thereof. The compounds of the invention are inhibitors of P13-kinase activity.

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