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N-(2-methoxy-4-nitro-phenyl)butanamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78701-56-1

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78701-56-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78701-56-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,7,0 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78701-56:
(7*7)+(6*8)+(5*7)+(4*0)+(3*1)+(2*5)+(1*6)=151
151 % 10 = 1
So 78701-56-1 is a valid CAS Registry Number.

78701-56-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Thymylbutyrat

1.2 Other means of identification

Product number -
Other names 4-butyrylamino-3-methoxy-nitrobenzene

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:78701-56-1 SDS

78701-56-1Relevant academic research and scientific papers

SUBSTITUTED P-DIAMINOBENZENE DERIVATIVES

-

Page/Page column 97-98, (2010/02/08)

The present invention relates to aniline derivatives of the general formula I or pharmaceutically acceptable salts thereof and their use.

Multi-step process for the production of methanesulfon-m-anisidide, 4'-(9-acridinylamino)-

-

, (2008/06/13)

A multi-step method of producing the compound methanesulfon-m-anisidide, 4''-(9-acridinylamino)-, acetate (VII), which may be in free base form and designated NSC 249992, also known as AMSA. This compound is produced by an elegant process from a starting material, 4-butyrylamino-3-methoxy-nitrobenzene, which is later transformed to methanesulfon-m-anisidide, 4''-amino- (IV) and is coupled or joined to 9-chloro-acridine, producing the chloride salt which is later converted to the acetate.

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