Cas 669763-71-7,Hydrazinecarbothioamide, 2-[2-[(4-chlorophenyl)methylene]cyclopentylidene]-

669763-71-7

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Basic information

Product Name: Hydrazinecarbothioamide, 2-[2-[(4-chlorophenyl)methylene]cyclopentylidene]-
Synonyms:
CAS NO:669763-71-7
Molecular Formula: C13H14ClN3S
Molecular Weight: 279.793
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Hydrazinecarbothioamide, 2-[2-[(4-chlorophenyl)methylene]cyclopentylidene]-(CAS DataBase Reference)
NIST Chemistry Reference: Hydrazinecarbothioamide, 2-[2-[(4-chlorophenyl)methylene]cyclopentylidene]-(669763-71-7)
EPA Substance Registry System: Hydrazinecarbothioamide, 2-[2-[(4-chlorophenyl)methylene]cyclopentylidene]-(669763-71-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 669763-71-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 669763-71-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,9,7,6 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 669763-71:
(8*6)+(7*6)+(6*9)+(5*7)+(4*6)+(3*3)+(2*7)+(1*1)=227
227 % 10 = 7
So 669763-71-7 is a valid CAS Registry Number.

669763-71-7Upstream product

669763-71-7Downstream Products

669763-71-7Relevant academic research and scientific papers

An investigation of the biological effect of structural modifications of isothiosemicarbazones and their cyclic analogues

Maccioni,Cardia,Distinto,Bonsignore,De Logu

, p. 951 - 959 (2003)

Several arylideneisothiosemicarbazones and arylidenehydrazothiazoles have been synthesised to obtain new antimicrobial agents. Their activity against both bacteria and fungi has been tested and some interesting informations about their biological activity

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