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Glycine, N-(4-acetylphenyl)-N-nitroso- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84968-84-3

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84968-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84968-84-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,9,6 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 84968-84:
(7*8)+(6*4)+(5*9)+(4*6)+(3*8)+(2*8)+(1*4)=193
193 % 10 = 3
So 84968-84-3 is a valid CAS Registry Number.

84968-84-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-nitroso-N-(4-acetylphenyl)glycine

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:84968-84-3 SDS

84968-84-3Relevant academic research and scientific papers

Synthesis and antimicrobial activity of 3-(substituted-phenyl)-sydnones

Moustafa,Eisa

, p. 397 - 401 (2007/10/02)

3-(3 or 4-Acetylphenyl)-sydnones 7, 8 have been synthesized by formation of the glycines 3, 4, followed by nitrosation to 5, 6 and cyclization with acetic anhydride to sydnones. Sydnone derivatives carrying chalcone moieties 15, 16 were prepared by format

Reactions of 3-(p-Acetylphenyl)sydnones: Part 1-Synthesis and Biological Evaluation of 3-(p-Acetylphenl)sydnone and Its Derivatives

Dambal, Devaraddi, B.,Badami, Bharati V.,Puranik, Gurubasav S.

, p. 865 - 868 (2007/10/02)

3-(p-Acetylphenyl)sydnone (7) undergoes condensation with aryl aldehydes to give the corresponding cinnamoyl derivatives (11-25).The reaction of sydnones (7-9) with hydroxylamine, phenylhydrazine, dimethyl acetylene-dicarboxylate and bromine gives the ket

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