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94205-71-7

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94205-71-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94205-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,2,0 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 94205-71:
(7*9)+(6*4)+(5*2)+(4*0)+(3*5)+(2*7)+(1*1)=127
127 % 10 = 7
So 94205-71-7 is a valid CAS Registry Number.

94205-71-7SDS

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 2-anilino-5-[(2-hydroxyphenyl)methylidene]-1,3-thiazol-4-one

1.2 Other means of identification

Product number -
Other names 4(5H)-Thiazolone,2-(phenylamino)-5-[(2-hydroxyphenyl)methylene]

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:94205-71-7 SDS

94205-71-7Downstream Products

94205-71-7Relevant articles and documents

Design, Synthesis and Pharmacological Screening of Novel Antihypertensive Agents Using Hybrid Approach

Bhandari, Shashikant V.,Bothara, Kailash G.,Patil, Ajit A.,Chitre, Trupti S.,Sarkate, Aniket P.,Gore, Suraj T.,Dangre, Sudarshan C.,Khachane, Chetan V.

experimental part, p. 390 - 400 (2011/02/25)

Eight derivatives of general formula 2-(2-(4-(3-((5-substituted methylene)-4-oxo-2-(phenylimino)thiazolidin-3-yl)-2-hydroxypropylamino)b enzoyl)hydrazinyl)-2-oxoethyl nitrate were synthesized and tested for electrocardiographic, antiarrhythmic, vasorelaxing and antihypertensive activity as well as for in-vitro nitric oxide (NO) releasing ability. Compound 8b 2-(2-(4-(3-(5-benzyliden-4-oxo-2-(phenylimino)thiazolidin-3-yl)-2-hydrox ypropylamino)benzoyl)hydrazinyl)-2-oxoethyl nitrate, was the most potent in this series. The pharmacological results suggested that the antiarrhythmic effects of these compounds were related to their adrenolytic properties which are believed to be due to the presence of the 5-(substituted)methylen-2-(phenylimino)thiazolidin-4-one moiety with less bulky, electron donating substituent on the phenyl ring at 5th position of the thiazolidin-4-one. In conclusion, most of the synthesized compounds were significantly potent as antiarrhythmic and antihypertensive; this might be due to the presence of different pharmacopores which might act at different locations with different mode of action. Further insights of the same can be obtained by doing investigation at receptor level. The potency of compounds 8a-8h were promising enough to continue further experiments.

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