Cas 138474-80-3,Carbamic acid, [1-(2,6-dimethoxy-2,5-cyclohexadien-1-yl)ethyl]-, 1,1-dimethylethyl ester, (S)-

138474-80-3

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Basic information

Product Name: Carbamic acid, [1-(2,6-dimethoxy-2,5-cyclohexadien-1-yl)ethyl]-, 1,1-dimethylethyl ester, (S)-
Synonyms:
CAS NO:138474-80-3
Molecular Formula: C15H25NO4
Molecular Weight: 283.368
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: Carbamic acid, [1-(2,6-dimethoxy-2,5-cyclohexadien-1-yl)ethyl]-, 1,1-dimethylethyl ester, (S)-(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [1-(2,6-dimethoxy-2,5-cyclohexadien-1-yl)ethyl]-, 1,1-dimethylethyl ester, (S)-(138474-80-3)
EPA Substance Registry System: Carbamic acid, [1-(2,6-dimethoxy-2,5-cyclohexadien-1-yl)ethyl]-, 1,1-dimethylethyl ester, (S)-(138474-80-3)

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: 138474-80-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 138474-80-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,7 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 138474-80:
(8*1)+(7*3)+(6*8)+(5*4)+(4*7)+(3*4)+(2*8)+(1*0)=153
153 % 10 = 3
So 138474-80-3 is a valid CAS Registry Number.

138474-80-3Upstream product

138474-80-3Downstream Products

6078-06-4 (S)-methyl 3-aminobutanoate

138474-80-3Relevant academic research and scientific papers

The directed cleavage of substituted 1-phenylethylamines: A novel route to enantiomerically pure β-amino acid esters and β-lactams

Bringmann,Geuder

, p. 829 - 831 (1991)

An efficient novel access to enantiomerically pure β-amino acid esters and β-lactams (e.g., methyl (3S,4S)-1-(tert-butyldimethylsilyl-4-methyl-2-oxoazetidine-3-carboxylat e) from optically active 1-arylethylamines is described. Regiospecific cleavage is performed by Birch reduction and subsequent ozonolysis.

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