Cas 488852-71-7,Carbamic acid, [(1S,2Z)-1-(phenylmethyl)-12-(triphenylmethoxy)-2-dodecenyl]-, 1,1-dimethylethyl ester

488852-71-7

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Basic information

Product Name: Carbamic acid, [(1S,2Z)-1-(phenylmethyl)-12-(triphenylmethoxy)-2-dodecenyl]-, 1,1-dimethylethyl ester
Synonyms:
CAS NO:488852-71-7
Molecular Formula: C43H53NO3
Molecular Weight: 631.899
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, [(1S,2Z)-1-(phenylmethyl)-12-(triphenylmethoxy)-2-dodecenyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [(1S,2Z)-1-(phenylmethyl)-12-(triphenylmethoxy)-2-dodecenyl]-, 1,1-dimethylethyl ester(488852-71-7)
EPA Substance Registry System: Carbamic acid, [(1S,2Z)-1-(phenylmethyl)-12-(triphenylmethoxy)-2-dodecenyl]-, 1,1-dimethylethyl ester(488852-71-7)

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: 488852-71-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 488852-71-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,8,8,5 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 488852-71:
(8*4)+(7*8)+(6*8)+(5*8)+(4*5)+(3*2)+(2*7)+(1*1)=217
217 % 10 = 7
So 488852-71-7 is a valid CAS Registry Number.

488852-71-7Upstream product

488852-71-7Downstream Products

488852-78-4 (12R)-12-[(tert-butoxycarbonyl)amino]-13-phenyltridecan-1-ol

488852-71-7Relevant academic research and scientific papers

An efficient method for the synthesis of enantiopure ω-amino acids with proteinogenic side chains

Noula, Caterina,Loukas, Vassilios,Kokotos, George

, p. 1735 - 1739 (2002)

An efficient method for the synthesis of enantiopure ω-amino acids with proteinogenic side chains, starting from the corresponding natural α-amino acids, was developed. N-Protected amino aldehydes, obtained from the corresponding amino alcohols by oxidati

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