Cas 124022-29-3,Acetic acid (1S,5R)-3-benzyl-5-hydroxymethyl-9-methylene-3-aza-bicyclo[3.3.1]non-1-ylmethyl ester

124022-29-3

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Basic information

Product Name: Acetic acid (1S,5R)-3-benzyl-5-hydroxymethyl-9-methylene-3-aza-bicyclo[3.3.1]non-1-ylmethyl ester
Synonyms: Acetic acid (1S,5R)-3-benzyl-5-hydroxymethyl-9-methylene-3-aza-bicyclo[3.3.1]non-1-ylmethyl ester
CAS NO:124022-29-3
Molecular Formula:
Molecular Weight: 329.439
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: Acetic acid (1S,5R)-3-benzyl-5-hydroxymethyl-9-methylene-3-aza-bicyclo[3.3.1]non-1-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (1S,5R)-3-benzyl-5-hydroxymethyl-9-methylene-3-aza-bicyclo[3.3.1]non-1-ylmethyl ester(124022-29-3)
EPA Substance Registry System: Acetic acid (1S,5R)-3-benzyl-5-hydroxymethyl-9-methylene-3-aza-bicyclo[3.3.1]non-1-ylmethyl ester(124022-29-3)

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: 124022-29-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 124022-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,0,2 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 124022-29:
(8*1)+(7*2)+(6*4)+(5*0)+(4*2)+(3*2)+(2*2)+(1*9)=73
73 % 10 = 3
So 124022-29-3 is a valid CAS Registry Number.

124022-29-3Upstream product

124022-29-3Downstream Products

124022-29-3Relevant academic research and scientific papers

Asymmetric total synthesis of atisine via intramolecular double Michael reaction

Ihara, Masataka,Suzuki, Makoto,Fukumoto, Keiichiro,Kabuto, Chizuko

, p. 1164 - 1171 (2007/10/02)

The bridged, pentacyclic intermediate 2 for atisine (1) was synthesized in a naturally occurring enantiomeric form from dimethyl cyclohexanone-2,6-dicarboxylate (6). The synthesis is composed of the following key steps: (1) formation of the azabicyclo[3.3

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