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83999-28-4

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83999-28-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83999-28-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,9 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 83999-28:
(7*8)+(6*3)+(5*9)+(4*9)+(3*9)+(2*2)+(1*8)=194
194 % 10 = 4
So 83999-28-4 is a valid CAS Registry Number.

83999-28-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-acetylphenyl)-3-oxobutanamide

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:83999-28-4 SDS

83999-28-4Relevant articles and documents

Gewald synthesis, antitumor profile and molecular modeling of novel 5-acetyl-4-((4-acetylphenyl)amino)-2-aminothiophene-3-carbonitrile scaffolds

Algothami, Wesam M.,Khalifa, Mohamed E.

, (2020)

Novel targets of 2-aminothiophene derivatives (2–9) were synthesized based upon preparation of the newly 5-acetyl-4-((4-acetylphenyl)amino)-2-aminothiophene-3-carbonitrile (2) using Gewald methodology. Several functional chemical reactions were performed

Synthesis of β-Ketoamide Curcumin Analogs for Anti-Diabetic and AGEs Inhibitory Activities

Banuppriya, Govindharasu,Sribalan, Rajendran,Fathima, Sulthan Alavudeen Rizwan,Padmini, Vediappen

, (2018/08/03)

Two different series of novel β-ketoamide curcumin analogs enriched in biological activities have been synthesized. The synthesized compounds were screened for their in?vitro anti-diabetic and AGEs inhibitory activities and exhibited potent to good anti-diabetic and AGEs inhibitory activities. The molecular docking study was also performed with the α-amylase enzyme.

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