Cas 145664-07-9,3-Phenyl-7-[1-phenyl-meth-(Z)-ylidene]-3,3a,4,5,6,7-hexahydro-indazole-2-carbothioic acid allylamide

145664-07-9

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Basic information

Product Name: 3-Phenyl-7-[1-phenyl-meth-(Z)-ylidene]-3,3a,4,5,6,7-hexahydro-indazole-2-carbothioic acid allylamide
Synonyms:
CAS NO:145664-07-9
Molecular Formula:
Molecular Weight: 387.549
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: 3-Phenyl-7-[1-phenyl-meth-(Z)-ylidene]-3,3a,4,5,6,7-hexahydro-indazole-2-carbothioic acid allylamide(CAS DataBase Reference)
NIST Chemistry Reference: 3-Phenyl-7-[1-phenyl-meth-(Z)-ylidene]-3,3a,4,5,6,7-hexahydro-indazole-2-carbothioic acid allylamide(145664-07-9)
EPA Substance Registry System: 3-Phenyl-7-[1-phenyl-meth-(Z)-ylidene]-3,3a,4,5,6,7-hexahydro-indazole-2-carbothioic acid allylamide(145664-07-9)

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: 145664-07-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 145664-07-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,6,6 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 145664-07:
(8*1)+(7*4)+(6*5)+(5*6)+(4*6)+(3*4)+(2*0)+(1*7)=139
139 % 10 = 9
So 145664-07-9 is a valid CAS Registry Number.

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145664-07-9Downstream Products

145664-07-9Relevant academic research and scientific papers

Synthesis and antidepressant activity of some new 8-thiocarbamoyl-7,8-diazabicyclo[4.3.0]non-6-ene derivatives

Bilgin,Yesilada,Palaska,Sunal

, p. 1271 - 1273 (2007/10/02)

Several 8-thiocarbamoyl-7,8-diazabicyclo[4.3.0]non-6-enes were prepared by condensing two α,β-unsaturated ketones (2-benzylidene and 2,6-dibenzylidene cyclohexanones) with hydrazine hydrate and reacting the resulting compounds with various isothiocyanates

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