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102227-52-1

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102227-52-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102227-52-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,2,2 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 102227-52:
(8*1)+(7*0)+(6*2)+(5*2)+(4*2)+(3*7)+(2*5)+(1*2)=71
71 % 10 = 1
So 102227-52-1 is a valid CAS Registry Number.

102227-52-1SDS

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 3-pyridin-4-yl-2H-1,2,4-oxadiazol-5-one

1.2 Other means of identification

Product number -
Other names 1,2,4-Oxadiazol-5(2H)-one,3-(4-pyridinyl)

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:102227-52-1 SDS

102227-52-1Downstream Products

102227-52-1Relevant articles and documents

Synthesis and antibacterial activity of novel pyridine and pyrazine derivatives obtained from amidoximes

Gobis, Katarzyna,Foks, Henryk,Kedzia, Anna,Wierzbowska, Maria,Zwolska, Zofia

experimental part, p. 1271 - 1279 (2010/03/23)

(Chemical Equation Presented) The new pyridine, 4-pyridine N-oxide and pyrazine derivatives exhibiting an antibacterial activity have been synthesized. Amidoximes were transformed into N-hydroxyimidoyl chlorides and then into appropriate oximes. Upon treatment of pyridinecaboxamidoximes with methyl iodide 1-methylpyridynium iodides were formed. Reaction of amidoximes with various carbamoyl chlorides led to corresponding 5-aminocarbonyl-1,2,4-oxadiazoles. Some of carboxamides have undergone thermal decarboxylation to tertiary amines. The newly synthesized compounds were tested in vitro for their tuberculostatic activity. MIC of the most active compound 9 was 12.5 μg/mL for H 37Rv strain. Their activity towards 25 strains of anaerobic and 25 strains of aerobic bacteria was also studied. Derivative 18 was active against both aerobic and anaerobic types of the bacteria.

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