Cas 142963-47-1,Glycine, N-[(1-ethenylcyclohexyl)methyl]-N-(methoxycarbonyl)-, methyl ester

142963-47-1

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Basic information

Product Name: Glycine, N-[(1-ethenylcyclohexyl)methyl]-N-(methoxycarbonyl)-, methyl ester
Synonyms:
CAS NO:142963-47-1
Molecular Formula: C14H23NO4
Molecular Weight: 269.341
EINECS: N/A
Product Categories: N/A
Mol File: 142963-47-1.mol

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: Glycine, N-[(1-ethenylcyclohexyl)methyl]-N-(methoxycarbonyl)-, methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Glycine, N-[(1-ethenylcyclohexyl)methyl]-N-(methoxycarbonyl)-, methyl ester(142963-47-1)
EPA Substance Registry System: Glycine, N-[(1-ethenylcyclohexyl)methyl]-N-(methoxycarbonyl)-, methyl ester(142963-47-1)

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: 142963-47-1(Hazardous Substances Data)

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Glycine, N-[(1-ethenylcyclohexyl)methyl]-N-(methoxycarbonyl)-, methyl ester
Cas No: 142963-47-1
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142963-47-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142963-47-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,9,6 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 142963-47:
(8*1)+(7*4)+(6*2)+(5*9)+(4*6)+(3*3)+(2*4)+(1*7)=141
141 % 10 = 1
So 142963-47-1 is a valid CAS Registry Number.

142963-47-1Upstream product

142963-38-0 (phenylthio)acetic acid methyl ester

142963-47-1Downstream Products

142963-47-1Relevant articles and documents

Reductive Cyclization of Carbon-Centered Glycine Radicals; A Novel Synthetic Route to Cyclic α-Amino Acids

Esch, Peter M.,Hiemstra, Henk,Boer, Richard F. de,Speckamp, W. Nico

, p. 4659 - 4676 (1992)

Reductive cyclizations (tributyltin hydride, AIBN) of several α-(phenylthio)glycine derivatives with a 3-alkenyl substituent at nitrogen are reported.These reactions proceed via 2-aza-5-alken-1-yl radicals as intermediates which bear electron-withdrawing

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