Cas 138877-87-9,4-(tert-Butylimino)-1-(2,6-dimethylphenyl)-5-hydroxy-2-(methylthio)-5-phenyl-2-imidazoline hydrochloride

138877-87-9

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Basic information

Product Name: 4-(tert-Butylimino)-1-(2,6-dimethylphenyl)-5-hydroxy-2-(methylthio)-5-phenyl-2-imidazoline hydrochloride
Synonyms:
CAS NO:138877-87-9
Molecular Formula:
Molecular Weight: 418.003
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: 4-(tert-Butylimino)-1-(2,6-dimethylphenyl)-5-hydroxy-2-(methylthio)-5-phenyl-2-imidazoline hydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: 4-(tert-Butylimino)-1-(2,6-dimethylphenyl)-5-hydroxy-2-(methylthio)-5-phenyl-2-imidazoline hydrochloride(138877-87-9)
EPA Substance Registry System: 4-(tert-Butylimino)-1-(2,6-dimethylphenyl)-5-hydroxy-2-(methylthio)-5-phenyl-2-imidazoline hydrochloride(138877-87-9)

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: 138877-87-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 138877-87-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,8,7 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 138877-87:
(8*1)+(7*3)+(6*8)+(5*8)+(4*7)+(3*7)+(2*8)+(1*7)=189
189 % 10 = 9
So 138877-87-9 is a valid CAS Registry Number.

138877-87-9Upstream product

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138877-87-9Relevant academic research and scientific papers

Three-Component Cyclocondensations. An Efficient Synthesis of 4-Amino-2-(methylthio)imidazolium Salts via the Reaction of Methyl Chlorothioimidates with Benzaldimines and Isocyanides. Autoxidation of the Imidazole Derivatives

Malvaut, Yvelise,Marchand, Evelyne,Morel, Georges

, p. 2121 - 2127 (2007/10/02)

Treatment of imino chlorosulfides 1 with a mixture of benzaldimine and isocyanide provides 4-aminoimidazolium chlorides 5.Presumably the reaction involves the N-imidoylbenzylideniminium chlorides 4 as transient intermediates. 1- and 3-tert-Butyl imidazoli

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