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2-Furanpropanoic acid, 5-(2-chlorophenyl)-a-oxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

674334-28-2

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674334-28-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 674334-28-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,4,3,3 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 674334-28:
(8*6)+(7*7)+(6*4)+(5*3)+(4*3)+(3*4)+(2*2)+(1*8)=172
172 % 10 = 2
So 674334-28-2 is a valid CAS Registry Number.

674334-28-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[5-(2-Chloro-phenyl)-furan-2-yl]-2-oxo-propionic acid

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:674334-28-2 SDS

674334-28-2Downstream Products

674334-28-2Relevant academic research and scientific papers

Synthesis of new biologically active arylfuranylmethyltriazinones and their antibacterial activity studies

Holla, B. Shivarama,Shivananda,Veerendra,Bhat, K. Subrahmanya

, p. 2649 - 2651 (2007/10/03)

In view of the pharmacological activities of 1,2,4-triazinones, a series of 4-amino-6-arylfuranylmethyl-3-mercapto-1,2,4-triazin-5(4H)-ones 7 have been synthesized by refluxing pyruvic acids 5 in ethanol with thiocarbohydrazide 6 on a steam-bath. The structures of 7 are confirmed by elemental analysis, IR, NMR and mass spectral data. Also, these compounds 7 have been screened for antibacterial activities against E. coli, S.aureus, P. aeruginosa and G. bacillus. Their MIC values are determined. The results indicate that among the compounds tested, compounds 7a and 7c carrying p-chloro and p-bromo substituents show excellent antibacterial activity against all the bacteria tested. It is concluded that compounds 7a, 7c, 7d and 7f may prove to be promising antibacterial agents.

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