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51419-40-0

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51419-40-0 Usage

General Description

N-(5-Nitro-thiophene-2-yl)-acetamide is a chemical compound with the formula C8H7N3O3S. It is a nitro-substituted thiophene derivative that is commonly used in the synthesis of pharmaceuticals and agrochemicals. N-(5-NITRO-THIOPHENE-2-YL)-ACETAMIDE is known for its antimicrobial and anti-inflammatory properties, making it valuable for the development of new drugs. N-(5-Nitro-thiophene-2-yl)-acetamide is also used as an intermediate in organic synthesis, particularly in the production of heterocyclic compounds. Its structure and properties make it a versatile building block for various chemical processes and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 51419-40-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,1 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 51419-40:
(7*5)+(6*1)+(5*4)+(4*1)+(3*9)+(2*4)+(1*0)=100
100 % 10 = 0
So 51419-40-0 is a valid CAS Registry Number.

51419-40-0SDS

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 N-(5-nitrothiophen-2-yl)acetamide

1.2 Other means of identification

Product number -
Other names 2-(Acetylamino)-5-nitrothiophene

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:51419-40-0 SDS

51419-40-0Relevant articles and documents

MODIFIED PROTEINS AND PROTEIN DEGRADERS

-

Paragraph 00785; 00790; 00791, (2021/12/08)

Provided herein are compounds, pharmaceutical compositions, and methods for binding or degrading target proteins. Further provided herein are compounds having a DNA damage-binding protein 1 (DDB1) binding moiety. Some such embodiments include a linker. Some such embodiments include a target protein binding moiety. Further provided herein are ligand-DDB1 complexes. Further provided herein are in vivo modified DDB1 proteins.

Functional Derivatives of Thiophene. I. Synthesis and 1H-NMR Spectra in the 2-Aminothiophene Series.

Galvez, C.,Garcia, F.

, p. 851 - 853 (2007/10/02)

The preparation of 2-amino-5-nitrothiophene, 2-formamido-5-nitrothiophene, 2-acetamido-5-nitrothiophene and 2-t-butoxycarbonylamino-5-nitrothiophene are described.Abnormal values of the coupling constants J3,4 had been observed in the 1H-NMR spectra of compounds obtained.

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