Cas 73992-23-1,benzyl<2,3β,3aα.4,5,6,7,8,9,9aβ-decahydro-4-oxothieno<3,2-c>azocin-3α-yl>carbamic acid methyl ester 1α-oxide

73992-23-1

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Basic information

Product Name: benzyl<2,3β,3aα.4,5,6,7,8,9,9aβ-decahydro-4-oxothieno<3,2-c>azocin-3α-yl>carbamic acid methyl ester 1α-oxide
Synonyms: benzyl<2,3β,3aα.4,5,6,7,8,9,9aβ-decahydro-4-oxothieno<3,2-c>azocin-3α-yl>carbamic acid methyl ester 1α-oxide
CAS NO:73992-23-1
Molecular Formula:
Molecular Weight: 364.466
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: benzyl<2,3β,3aα.4,5,6,7,8,9,9aβ-decahydro-4-oxothieno<3,2-c>azocin-3α-yl>carbamic acid methyl ester 1α-oxide(CAS DataBase Reference)
NIST Chemistry Reference: benzyl<2,3β,3aα.4,5,6,7,8,9,9aβ-decahydro-4-oxothieno<3,2-c>azocin-3α-yl>carbamic acid methyl ester 1α-oxide(73992-23-1)
EPA Substance Registry System: benzyl<2,3β,3aα.4,5,6,7,8,9,9aβ-decahydro-4-oxothieno<3,2-c>azocin-3α-yl>carbamic acid methyl ester 1α-oxide(73992-23-1)

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: 73992-23-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 73992-23-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,9,9 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73992-23:
(7*7)+(6*3)+(5*9)+(4*9)+(3*2)+(2*2)+(1*3)=161
161 % 10 = 1
So 73992-23-1 is a valid CAS Registry Number.

73992-23-1Upstream product

73992-10-6 benzyl<2,3β,3aβ,5,6,7,8,8aβ-octahydro-4-hydroxyimino-4H-cycloheptathiophen-3α-yl>carbamic acid methyl ester 1α-oxide

73992-23-1Downstream Products

73992-23-1Relevant academic research and scientific papers

Olefinic Nitrone and Nitrile Oxide Cycloadditions. A Short Stereospecific Synthesis of Biotin from Cycloheptene

Confalone, Pat N.,Pizzolato, Giacomo,Confalone, Dianne Lollar,Uskokovic Milan R.

, p. 1954 - 1960 (1980)

A novel synthesis of biotine (6) from cycloheptene (4) via the key amino alcohol 5 is described.The synthetic scheme is based upon an intramolecular nitrone-olefin cycloaddition of the reactive intermediate 13, generated in situ from the aldehyde

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