Cas 163812-01-9,Benzoic acid (1R,7S,8S,8aS)-7,8-dihydroxy-3-oxo-octahydro-indolizin-1-yl ester

163812-01-9

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Basic information

Product Name: Benzoic acid (1R,7S,8S,8aS)-7,8-dihydroxy-3-oxo-octahydro-indolizin-1-yl ester
Synonyms:
CAS NO:163812-01-9
Molecular Formula:
Molecular Weight: 291.304
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: Benzoic acid (1R,7S,8S,8aS)-7,8-dihydroxy-3-oxo-octahydro-indolizin-1-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (1R,7S,8S,8aS)-7,8-dihydroxy-3-oxo-octahydro-indolizin-1-yl ester(163812-01-9)
EPA Substance Registry System: Benzoic acid (1R,7S,8S,8aS)-7,8-dihydroxy-3-oxo-octahydro-indolizin-1-yl ester(163812-01-9)

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: 163812-01-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 163812-01-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,8,1 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 163812-01:
(8*1)+(7*6)+(6*3)+(5*8)+(4*1)+(3*2)+(2*0)+(1*1)=119
119 % 10 = 9
So 163812-01-9 is a valid CAS Registry Number.

163812-01-9Upstream product

163812-00-8 Benzoic acid (1aR,6R,6aR,6bS)-4-oxo-octahydro-1-oxa-3a-aza-cyclopropa[e]inden-6-yl ester

163812-01-9Downstream Products

163812-01-9Relevant academic research and scientific papers

Stereocontrolled syntheses of polyhydroxy indolizidines, including 8a-epi-, 6,8a-diepi- and 1,6-diepi-castanospermine, starting from malic acid

Leeper, Finian J.,Howard, Steven

, p. 2335 - 2338 (2007/10/02)

Stereocontrolled total syntheses of one trihydroxy indolizidine 15 and three tetrahydroxy indolizidines, 17, 21 and 23 - all diastereoisomers of castanospermine - are described which use malic acid as the only chiral starting material.

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