Cas 87022-93-3,1-[3-(2,3,5,6-Tetrahydro-imidazo[2,1-b]thiazol-6-yl)-phenyl]-3-(4-trifluoromethyl-phenyl)-thiourea

87022-93-3

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Basic information

Product Name: 1-[3-(2,3,5,6-Tetrahydro-imidazo[2,1-b]thiazol-6-yl)-phenyl]-3-(4-trifluoromethyl-phenyl)-thiourea
Synonyms:
CAS NO:87022-93-3
Molecular Formula:
Molecular Weight: 422.498
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: 1-[3-(2,3,5,6-Tetrahydro-imidazo[2,1-b]thiazol-6-yl)-phenyl]-3-(4-trifluoromethyl-phenyl)-thiourea(CAS DataBase Reference)
NIST Chemistry Reference: 1-[3-(2,3,5,6-Tetrahydro-imidazo[2,1-b]thiazol-6-yl)-phenyl]-3-(4-trifluoromethyl-phenyl)-thiourea(87022-93-3)
EPA Substance Registry System: 1-[3-(2,3,5,6-Tetrahydro-imidazo[2,1-b]thiazol-6-yl)-phenyl]-3-(4-trifluoromethyl-phenyl)-thiourea(87022-93-3)

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: 87022-93-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 87022-93-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,0,2 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87022-93:
(7*8)+(6*7)+(5*0)+(4*2)+(3*2)+(2*9)+(1*3)=133
133 % 10 = 3
So 87022-93-3 is a valid CAS Registry Number.

87022-93-3Upstream product

87022-93-3Downstream Products

87022-93-3Relevant academic research and scientific papers

Isothiourea Derivatives of 6-Phenyl-2,3,5,6-tetrahydroimidazothiazole with Broad-Spectrum Anthelmintic Activity

Brewer, Malcolm D.,Dorgan, Roderick J.J.,Manger, Brian R.,Mamalis, Patrick,Webster, Richard A.B.

, p. 1848 - 1853 (2007/10/02)

A series of isothiourea derivatives of 6-phenyl-2,3,5,6-tetrahydroimidazothiazole (tetramisole) is described.The compounds are prepared by the S-alkylation of the thioureas that were obtained either by the reaction of an amine with 6-(3-isothiocyan

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