Cas 1168102-72-4,(R)-3-(methoxycarbonylphenylmethyl)-5-methyl-3H-imidazole-4-carboxylic acid ethyl ester

1168102-72-4

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Basic information

Product Name: (R)-3-(methoxycarbonylphenylmethyl)-5-methyl-3H-imidazole-4-carboxylic acid ethyl ester
Synonyms:
CAS NO:1168102-72-4
Molecular Formula:
Molecular Weight: 302.33
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: (R)-3-(methoxycarbonylphenylmethyl)-5-methyl-3H-imidazole-4-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-3-(methoxycarbonylphenylmethyl)-5-methyl-3H-imidazole-4-carboxylic acid ethyl ester(1168102-72-4)
EPA Substance Registry System: (R)-3-(methoxycarbonylphenylmethyl)-5-methyl-3H-imidazole-4-carboxylic acid ethyl ester(1168102-72-4)

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: 1168102-72-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1168102-72-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,8,1,0 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1168102-72:
(9*1)+(8*1)+(7*6)+(6*8)+(5*1)+(4*0)+(3*2)+(2*7)+(1*2)=134
134 % 10 = 4
So 1168102-72-4 is a valid CAS Registry Number.

1168102-72-4Upstream product

50-00-0 formaldehyd

1168102-72-4Downstream Products

1168102-72-4Relevant academic research and scientific papers

α-Aminoester-derived imidazoles by 1,5-electrocyclization of azavinyl azomethine ylides

Attanasi, Orazio A.,Caselli, Emilia,Davoli, Paolo,Favi, Gianfranco,Mantellini, Fabio,Ori, Claudia,Prati, Fabio

, p. 2840 - 2843 (2009)

An efficient and practical method for the preparation of α-lmldazol-1-yl esters from 1,2-dlaza-1,3-dlenes (DDs), α-amlno esters, and aldehydes Is described. The overall sequence features a Michael-type conjugate addition between the a-amlno ester and the

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