Cas 1451067-49-4,methyl 6-{(2R,5S,6S)-1-[(benzyloxy)carbonyl]-5-hydroxy-6-methylpiperidine-2-yl}hexanoate

1451067-49-4

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Basic information

Product Name: methyl 6-{(2R,5S,6S)-1-[(benzyloxy)carbonyl]-5-hydroxy-6-methylpiperidine-2-yl}hexanoate
Synonyms: methyl 6-{(2R,5S,6S)-1-[(benzyloxy)carbonyl]-5-hydroxy-6-methylpiperidine-2-yl}hexanoate
CAS NO:1451067-49-4
Molecular Formula:
Molecular Weight: 377.481
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: methyl 6-{(2R,5S,6S)-1-[(benzyloxy)carbonyl]-5-hydroxy-6-methylpiperidine-2-yl}hexanoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 6-{(2R,5S,6S)-1-[(benzyloxy)carbonyl]-5-hydroxy-6-methylpiperidine-2-yl}hexanoate(1451067-49-4)
EPA Substance Registry System: methyl 6-{(2R,5S,6S)-1-[(benzyloxy)carbonyl]-5-hydroxy-6-methylpiperidine-2-yl}hexanoate(1451067-49-4)

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: 1451067-49-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1451067-49-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,1,0,6 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1451067-49:
(9*1)+(8*4)+(7*5)+(6*1)+(5*0)+(4*6)+(3*7)+(2*4)+(1*9)=144
144 % 10 = 4
So 1451067-49-4 is a valid CAS Registry Number.

1451067-49-4Upstream product

1451067-49-4Downstream Products

622836-88-8 6-{(2R,5S,6S)-1-[(benzyloxy)carbonyl]-5-hydroxy-6-methylpiperidine-2-yl}hexanoic acid

1451067-49-4Relevant academic research and scientific papers

Total synthesis of (+)-azimine via diastereoselective aminopalladation

Kurogome, Yuji,Kogiso, Masaya,Looi, Kok Kong,Hattori, Yasunao,Konno, Hiroyuki,Hirota, Mitsuru,Makabe, Hidefumi

, p. 8349 - 8352 (2013)

The aminopalladation of amino allylic alcohol using Cl2Pd(MeCN) 2 in CH2Cl2 gave the 2,6-disubstituted piperidine with excellent diastereoselectivity. This compound was successfully converted into (+)-azimine (1

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