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120399-38-4

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  • Propanimidamide,3-[[[2-[(aminoiminomethyl)amino]-5-thiazolyl]methyl]thio]-N-cyano-

    Cas No: 120399-38-4

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120399-38-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120399-38-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,3,9 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 120399-38:
(8*1)+(7*2)+(6*0)+(5*3)+(4*9)+(3*9)+(2*3)+(1*8)=114
114 % 10 = 4
So 120399-38-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H13N7S2/c10-5-15-7(11)1-2-17-4-6-3-14-9(18-6)16-8(12)13/h3H,1-2,4H2,(H2,11,15)(H4,12,13,14,16)

120399-38-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-cyano-3-[[2-(diaminomethylideneamino)-1,3-thiazol-5-yl]methylsulfanyl]propanimidamide

1.2 Other means of identification

Product number -
Other names Cgtmpa

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:120399-38-4 SDS

120399-38-4Downstream Products

120399-38-4Relevant articles and documents

H2-antagonists: Synthesis and activity of 2-Amino-5-thiazolyl derivatives

Plazzi,Bordi,Silva,Morini,Catellani,Vaona,Impicciatore

, p. 1011 - 1030 (2007/10/02)

2-Amino- and 2-guanidinothiazole derivatives having in position 5 a methylthioalkyl side-chain with urea-equivalent moieties were prepared for comparison with H2-antagonists of cimetidine and tiotidine series. Examination of the pharmacological results obtained from experiments on guinea pig atria and in cat gastric fistula, suggests some general observations about the structure-activity relationship of the compounds synthesized. The activity trend of these products is different from that of H2-imidazole antagonists while it is similar to that of the tiotidine series. Unlike the tiotidine similar compounds, the 2-guanidino-5-thiazolyl derivatives are less potent than the corresponding 2-amino-5-thiazolyl products. The activity of the latter ones is reduced in comparison to that of tiotidine or cimetidine.

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