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502178-78-1

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502178-78-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 502178-78-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,2,1,7 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 502178-78:
(8*5)+(7*0)+(6*2)+(5*1)+(4*7)+(3*8)+(2*7)+(1*8)=131
131 % 10 = 1
So 502178-78-1 is a valid CAS Registry Number.

502178-78-1SDS

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 5-methyl-N-ethyl-2-nitroaniline

1.2 Other means of identification

Product number -
Other names N-ethyl-5-methyl-2-nitro-aniline

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:502178-78-1 SDS

502178-78-1Relevant articles and documents

ACETYL-COA SYNTHETASE 2 (ACSS2) INHIBITORS AND METHODS USING SAME

-

Page/Page column 71-72, (2020/12/30)

The present disclosure provides compounds that are ACSS2 inhibitors. In certain embodiments, the compounds of the disclosure are useful for treating and/or preventing certain types of cancer.

Improved synthesis of functionalized mesogenic 2,6-bisbenzimidazolylpyridine ligands

McKenzie, Blayne M.,Miller, Adriane K.,Wojtecki, Rudy J.,Johnson, J. Casey,Burke, Kelly A.,Tzeng, Karis A.,Mather, Patrick T.,Rowan, Stuart J.

, p. 8488 - 8495 (2008/12/20)

A versatile one-pot synthetic platform for the preparation of a range of functionalized 2,6-bisbenzimidazolylpyridine (Bip) derivatives is presented. This protocol significantly reduces the cost and time of previous synthetic routes, while facilitating sc

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