Cas 120566-63-4,(+/-)-exo-8-Methyl-2,4-dioxo-3-(phenylmethyl)-3,8-diazabicyclo<3.2.1>octane-6-carboxylic acid methyl ester

120566-63-4

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Basic information

Product Name: (+/-)-exo-8-Methyl-2,4-dioxo-3-(phenylmethyl)-3,8-diazabicyclo<3.2.1>octane-6-carboxylic acid methyl ester
Synonyms:
CAS NO:120566-63-4
Molecular Formula:
Molecular Weight: 302.33
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: (+/-)-exo-8-Methyl-2,4-dioxo-3-(phenylmethyl)-3,8-diazabicyclo<3.2.1>octane-6-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (+/-)-exo-8-Methyl-2,4-dioxo-3-(phenylmethyl)-3,8-diazabicyclo<3.2.1>octane-6-carboxylic acid methyl ester(120566-63-4)
EPA Substance Registry System: (+/-)-exo-8-Methyl-2,4-dioxo-3-(phenylmethyl)-3,8-diazabicyclo<3.2.1>octane-6-carboxylic acid methyl ester(120566-63-4)

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: 120566-63-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 120566-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,5,6 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 120566-63:
(8*1)+(7*2)+(6*0)+(5*5)+(4*6)+(3*6)+(2*6)+(1*3)=104
104 % 10 = 4
So 120566-63-4 is a valid CAS Registry Number.

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120566-63-4Relevant academic research and scientific papers

An Approach to the 3,8-Diazabicyclooctane Moiety of Naphthyridinomycin and Quinocarcin via 1,3-Dipolar Cycloaddition of Photochemically Generated Azomethine Ylides.

Garner, Philip,Sunitha, K.,Shanthilal, T.

, p. 3525 - 3528 (2007/10/02)

An attractive strategy for construction of the 3,8-diazabicyclooctane moiety of targets 1 and 2 involving the 1,3-dipolar cycloaddition of photochemical generated azomethine ylides is presented.

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