Cas 1007352-83-1,(1R,2R,8aS)-2-hydroxy-1-(4-methylbenzoyloxy)-octahydro-1H-indolizinium chloride

1007352-83-1

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Basic information

Product Name: (1R,2R,8aS)-2-hydroxy-1-(4-methylbenzoyloxy)-octahydro-1H-indolizinium chloride
Synonyms: (1R,2R,8aS)-2-hydroxy-1-(4-methylbenzoyloxy)-octahydro-1H-indolizinium chloride
CAS NO:1007352-83-1
Molecular Formula:
Molecular Weight: 311.809
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,8aS)-2-hydroxy-1-(4-methylbenzoyloxy)-octahydro-1H-indolizinium chloride(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R,8aS)-2-hydroxy-1-(4-methylbenzoyloxy)-octahydro-1H-indolizinium chloride(1007352-83-1)
EPA Substance Registry System: (1R,2R,8aS)-2-hydroxy-1-(4-methylbenzoyloxy)-octahydro-1H-indolizinium chloride(1007352-83-1)

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: 1007352-83-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1007352-83-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,7,3,5 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1007352-83:
(9*1)+(8*0)+(7*0)+(6*7)+(5*3)+(4*5)+(3*2)+(2*8)+(1*3)=111
111 % 10 = 1
So 1007352-83-1 is a valid CAS Registry Number.

1007352-83-1Upstream product

1007352-82-0 (1R,2R)-2-hydroxy-1-(4-methylbenzoyloxy)-2,3-dihydro-1H-indolizinium chloride

1007352-83-1Downstream Products

1007352-83-1Relevant academic research and scientific papers

A concise synthesis of lentiginosine derivatives using a pyridinium formation via the Mitsunobu reaction

Azzouz, Rabah,Fruit, Corinne,Bischoff, Laurent,Marsais, Francis

, p. 1154 - 1157 (2008/09/18)

(Chemical Equation Presented) A four-step synthesis of (-)-lentiginosine and its epimers is described starting from 2-bromopyridine. The key step consisted of a quaternarization of a fully unprotected pyridinium-polyol unit using Mitsunobu methodology. Su

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