Cas 172035-01-7,(1R,4R,5R,8S)-(+)-7-benzyl-2-tert-butyl-4-ethoxycarbonyl-8-methyl-3-oxa-2,7-diazabicyclo<3.3.0>octane

172035-01-7

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Basic information

Product Name: (1R,4R,5R,8S)-(+)-7-benzyl-2-tert-butyl-4-ethoxycarbonyl-8-methyl-3-oxa-2,7-diazabicyclo<3.3.0>octane
Synonyms: (1R,4R,5R,8S)-(+)-7-benzyl-2-tert-butyl-4-ethoxycarbonyl-8-methyl-3-oxa-2,7-diazabicyclo<3.3.0>octane
CAS NO:172035-01-7
Molecular Formula:
Molecular Weight: 346.47
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,4R,5R,8S)-(+)-7-benzyl-2-tert-butyl-4-ethoxycarbonyl-8-methyl-3-oxa-2,7-diazabicyclo<3.3.0>octane(CAS DataBase Reference)
NIST Chemistry Reference: (1R,4R,5R,8S)-(+)-7-benzyl-2-tert-butyl-4-ethoxycarbonyl-8-methyl-3-oxa-2,7-diazabicyclo<3.3.0>octane(172035-01-7)
EPA Substance Registry System: (1R,4R,5R,8S)-(+)-7-benzyl-2-tert-butyl-4-ethoxycarbonyl-8-methyl-3-oxa-2,7-diazabicyclo<3.3.0>octane(172035-01-7)

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: 172035-01-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 172035-01-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,0,3 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 172035-01:
(8*1)+(7*7)+(6*2)+(5*0)+(4*3)+(3*5)+(2*0)+(1*1)=97
97 % 10 = 7
So 172035-01-7 is a valid CAS Registry Number.

172035-01-7Upstream product

16649-50-6 N-tert-Butylhydroxylamine

172035-01-7Downstream Products

172035-01-7Relevant academic research and scientific papers

Enantiomerically Pure 3-Oxa-2,7-diazabicyclooctanes: Preparation, Analysis of Conformation and Test for Enantioselective Catalysis

Aurich, Hans Guenter,Gentes, Christian,Harms, Klaus

, p. 10497 - 10512 (1995)

Amino alcohols 5 were prepared by various methods starting from (S)-(+)-alanine and (S)-(+)-valine.Swern oxidation of 5 afforded aldehydes 6 which were treated without isolation with N-alkylhydroxylamines to give nitrones 7A, B.These underwent spontaneous

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