Cas 1338481-40-5,(2S,3R,4R)-1-(N-methyl-N-((R)-1-phenylethyl)amino)-3-(benzyloxy)-4-methylhex-5-en-2-yl acetate

1338481-40-5

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Basic information

Product Name: (2S,3R,4R)-1-(N-methyl-N-((R)-1-phenylethyl)amino)-3-(benzyloxy)-4-methylhex-5-en-2-yl acetate
Synonyms: (2S,3R,4R)-1-(N-methyl-N-((R)-1-phenylethyl)amino)-3-(benzyloxy)-4-methylhex-5-en-2-yl acetate
CAS NO:1338481-40-5
Molecular Formula:
Molecular Weight: 395.542
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: (2S,3R,4R)-1-(N-methyl-N-((R)-1-phenylethyl)amino)-3-(benzyloxy)-4-methylhex-5-en-2-yl acetate(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3R,4R)-1-(N-methyl-N-((R)-1-phenylethyl)amino)-3-(benzyloxy)-4-methylhex-5-en-2-yl acetate(1338481-40-5)
EPA Substance Registry System: (2S,3R,4R)-1-(N-methyl-N-((R)-1-phenylethyl)amino)-3-(benzyloxy)-4-methylhex-5-en-2-yl acetate(1338481-40-5)

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: 1338481-40-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1338481-40-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,8,4,8 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1338481-40:
(9*1)+(8*3)+(7*3)+(6*8)+(5*4)+(4*8)+(3*1)+(2*4)+(1*0)=165
165 % 10 = 5
So 1338481-40-5 is a valid CAS Registry Number.

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1338481-40-5Relevant academic research and scientific papers

N-Methylative aziridine ring opening and asymmetric synthesis of MeBmt

Kim, Yongeun,Yoon, Doo-Ha,Ha, Hyun-Joon,Kang, Kyung Yeon,Lee, Won Koo

, p. 5918 - 5920 (2011)

Asymmetric synthesis of MeBmt, an unusual amino acid constituent of cyclosporine A, was achieved from aziridine-(2R)-carboxaldehyde through the highly stereoselective addition of (E)-crotylboronate and the subsequent N-methylative aziridine ring opening as key steps.

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