Cas 189443-26-3,Hydrazinecarbodithioic acid, [2-(2-cyclopenten-1-yl)-1-(5-methyl-2-furanyl)ethylidene]phenyl-, methyl ester

189443-26-3

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Basic information

Product Name: Hydrazinecarbodithioic acid, [2-(2-cyclopenten-1-yl)-1-(5-methyl-2-furanyl)ethylidene]phenyl-, methyl ester
Synonyms:
CAS NO:189443-26-3
Molecular Formula: C20H22N2OS2
Molecular Weight: 370.539
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: Hydrazinecarbodithioic acid, [2-(2-cyclopenten-1-yl)-1-(5-methyl-2-furanyl)ethylidene]phenyl-, methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Hydrazinecarbodithioic acid, [2-(2-cyclopenten-1-yl)-1-(5-methyl-2-furanyl)ethylidene]phenyl-, methyl ester(189443-26-3)
EPA Substance Registry System: Hydrazinecarbodithioic acid, [2-(2-cyclopenten-1-yl)-1-(5-methyl-2-furanyl)ethylidene]phenyl-, methyl ester(189443-26-3)

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: 189443-26-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 189443-26-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,4,4 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 189443-26:
(8*1)+(7*8)+(6*9)+(5*4)+(4*4)+(3*3)+(2*2)+(1*6)=173
173 % 10 = 3
So 189443-26-3 is a valid CAS Registry Number.

189443-26-3Upstream product

59-88-1 phenylhydrazine hydrochloride

189443-26-3Downstream Products

189443-26-3Relevant academic research and scientific papers

Iminyl radical generation via iminodithiocarbonate group transfer

Callier-Dublanchet, Anne-Claude,Quiclet-Sire, Beatrice,Zard, Samir Z.

, p. 2463 - 2466 (1997)

Irradiation with a sun lamp of thiocarbazone derivatives related to 1a in the presence of small amounts of hexabutylditin provides adducts arising from the reaction of an iminyl radical followed by transfer of an iminodithiocarbonate group.

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