Cas 630093-13-9,(1R,2R,6S,7S)-4-[2-(3,4-Dimethoxy-phenyl)-ethyl]-5-hydroxy-5-methyl-2-trimethylsilanyl-4-aza-tricyclo[5.2.1.0<sup>2,6</sup>]dec-8-en-3-one

630093-13-9

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Basic information

Product Name: (1R,2R,6S,7S)-4-[2-(3,4-Dimethoxy-phenyl)-ethyl]-5-hydroxy-5-methyl-2-trimethylsilanyl-4-aza-tricyclo[5.2.1.0^2,6]dec-8-en-3-one
Synonyms: (1R,2R,6S,7S)-4-[2-(3,4-Dimethoxy-phenyl)-ethyl]-5-hydroxy-5-methyl-2-trimethylsilanyl-4-aza-tricyclo[5.2.1.0^2,6]dec-8-en-3-one
CAS NO:630093-13-9
Molecular Formula:
Molecular Weight: 415.605
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: (1R,2R,6S,7S)-4-[2-(3,4-Dimethoxy-phenyl)-ethyl]-5-hydroxy-5-methyl-2-trimethylsilanyl-4-aza-tricyclo[5.2.1.0^2,6]dec-8-en-3-one(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R,6S,7S)-4-[2-(3,4-Dimethoxy-phenyl)-ethyl]-5-hydroxy-5-methyl-2-trimethylsilanyl-4-aza-tricyclo[5.2.1.0^2,6]dec-8-en-3-one(630093-13-9)
EPA Substance Registry System: (1R,2R,6S,7S)-4-[2-(3,4-Dimethoxy-phenyl)-ethyl]-5-hydroxy-5-methyl-2-trimethylsilanyl-4-aza-tricyclo[5.2.1.0^2,6]dec-8-en-3-one(630093-13-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 630093-13-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 630093-13-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,0,0,9 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 630093-13:
(8*6)+(7*3)+(6*0)+(5*0)+(4*9)+(3*3)+(2*1)+(1*3)=119
119 % 10 = 9
So 630093-13-9 is a valid CAS Registry Number.

630093-13-9Upstream product

75-16-1 methylmagnesium bromide

630093-13-9Downstream Products

630093-13-9Relevant academic research and scientific papers

Asymmetric synthesis of the erythrinan alkaloid system using a chiral lithium amide base desymmetrisation as the key step

Gill, Christopher,Greenhalgh, Daniel A.,Simpkins, Nigel S.

, p. 7803 - 7807 (2003)

A new asymmetric approach to the erythrinan alkaloid system is described, which involves chiral base desymmetrisation of a ring fused imide and a 6-exo-trig radical cyclisation as the key steps.

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