Cas 1104201-91-3,((2R,3R)-3-((E)-pentadec-1-enyl)oxiran-2-yl)methyl benzylcarbamate

1104201-91-3

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Basic information

Product Name: ((2R,3R)-3-((E)-pentadec-1-enyl)oxiran-2-yl)methyl benzylcarbamate
Synonyms: ((2R,3R)-3-((E)-pentadec-1-enyl)oxiran-2-yl)methyl benzylcarbamate
CAS NO:1104201-91-3
Molecular Formula:
Molecular Weight: 415.616
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: ((2R,3R)-3-((E)-pentadec-1-enyl)oxiran-2-yl)methyl benzylcarbamate(CAS DataBase Reference)
NIST Chemistry Reference: ((2R,3R)-3-((E)-pentadec-1-enyl)oxiran-2-yl)methyl benzylcarbamate(1104201-91-3)
EPA Substance Registry System: ((2R,3R)-3-((E)-pentadec-1-enyl)oxiran-2-yl)methyl benzylcarbamate(1104201-91-3)

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: 1104201-91-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1104201-91-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,4,2,0 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1104201-91:
(9*1)+(8*1)+(7*0)+(6*4)+(5*2)+(4*0)+(3*1)+(2*9)+(1*1)=73
73 % 10 = 3
So 1104201-91-3 is a valid CAS Registry Number.

1104201-91-3Upstream product

1104201-87-7 formylmethyl benzylcarbamate

1104201-91-3Downstream Products

724702-24-3 (S)-3-benzyl-4-((R,E)-1-hydroxyhexadec-2-enyl)oxazolidin-2-one

1104201-91-3Relevant academic research and scientific papers

Asymmetric sulfur ylide based enantioselective synthesis of D-erythro-sphingosine

Morales-Serna, Jose Antonio,Llaveria, Josep,Diaz, Yolanda,Matheu, M. Isabel,Castillon, Sergio

supporting information; experimental part, p. 4502 - 4504 (2009/03/12)

An asymmetric sulfur ylide reaction was employed to prepare an epoxide intermediate in a convergent manner. This epoxide was efficiently transformed into D-erythro-sphingosine.

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