Cas 132820-84-9,(3aS,4R,6aR)-4-((R)-3-Hydroxy-1-methoxymethoxy-propyl)-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyrrole-5-carboxylic acid benzyl ester

132820-84-9

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Basic information

Product Name: (3aS,4R,6aR)-4-((R)-3-Hydroxy-1-methoxymethoxy-propyl)-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyrrole-5-carboxylic acid benzyl ester
Synonyms:
CAS NO:132820-84-9
Molecular Formula:
Molecular Weight: 395.453
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: (3aS,4R,6aR)-4-((R)-3-Hydroxy-1-methoxymethoxy-propyl)-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyrrole-5-carboxylic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3aS,4R,6aR)-4-((R)-3-Hydroxy-1-methoxymethoxy-propyl)-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyrrole-5-carboxylic acid benzyl ester(132820-84-9)
EPA Substance Registry System: (3aS,4R,6aR)-4-((R)-3-Hydroxy-1-methoxymethoxy-propyl)-2,2-dimethyl-tetrahydro-[1,3]dioxolo[4,5-c]pyrrole-5-carboxylic acid benzyl ester(132820-84-9)

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: 132820-84-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 132820-84-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,8,2 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132820-84:
(8*1)+(7*3)+(6*2)+(5*8)+(4*2)+(3*0)+(2*8)+(1*4)=109
109 % 10 = 9
So 132820-84-9 is a valid CAS Registry Number.

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132820-84-9Relevant academic research and scientific papers

A new approach to swainsonine and castanospermine analogues

Burgess, Kevin,Henderson, Ian

, p. 6949 - 6952 (1990)

(1S, 2R, 7R, 7aR)- 1,2,7-Trihydroxypyrrolizidine (1) is prepared by elaboration of an erythrose derivative (4) via an asymmetric allylation reaction; this approach promises to be widely applicable to syntheses of polyhydroxylated indolizidine and pyrroliz

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