Cas 141945-22-4,1H-Imidazole-4-carboxamide, 2,2'-[methylenebis(thio)]bis[N-(phenylmethyl)-1-(2-pyrimidinyl)-

141945-22-4

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Basic information

Product Name: 1H-Imidazole-4-carboxamide, 2,2'-[methylenebis(thio)]bis[N-(phenylmethyl)-1-(2-pyrimidinyl)-
Synonyms:
CAS NO:141945-22-4
Molecular Formula: C31H26N10O2S2
Molecular Weight: 634.745
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: 1H-Imidazole-4-carboxamide, 2,2'-[methylenebis(thio)]bis[N-(phenylmethyl)-1-(2-pyrimidinyl)-(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Imidazole-4-carboxamide, 2,2'-[methylenebis(thio)]bis[N-(phenylmethyl)-1-(2-pyrimidinyl)-(141945-22-4)
EPA Substance Registry System: 1H-Imidazole-4-carboxamide, 2,2'-[methylenebis(thio)]bis[N-(phenylmethyl)-1-(2-pyrimidinyl)-(141945-22-4)

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: 141945-22-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141945-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,9,4 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 141945-22:
(8*1)+(7*4)+(6*1)+(5*9)+(4*4)+(3*5)+(2*2)+(1*2)=124
124 % 10 = 4
So 141945-22-4 is a valid CAS Registry Number.

141945-22-4Upstream product

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141945-22-4Relevant academic research and scientific papers

Amino Acids in the Synthesis of Heterocyclic Compounds. Transformations of Thiazolones into Imidazole Derivatives

Copar, Anton,Stanovnik, Branko,Tisler, Miha

, p. 155 - 160 (2007/10/02)

5(4H)-Thiazolone derivative 4, obtained from N-dithiocarbobenzoxyglycine (1) and N,N-dimethyl-N'-heteroarylformamidines 3 in acetic anhydride, was rearranged with sodium methoxide in methanol followed by acidification with acetic acid into imidazole-4-car

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