Cas 756499-83-9,1-(10,10-dimethyl-2-oxo-3-phenyl-3,4-diazatricyclo[5.2.1.0<sup>1,5</sup>]dec-4-yl)-2-phenylethane-1,2-dione

756499-83-9

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Basic information

Product Name: 1-(10,10-dimethyl-2-oxo-3-phenyl-3,4-diazatricyclo[5.2.1.0^1,5]dec-4-yl)-2-phenylethane-1,2-dione
Synonyms: 1-(10,10-dimethyl-2-oxo-3-phenyl-3,4-diazatricyclo[5.2.1.0^1,5]dec-4-yl)-2-phenylethane-1,2-dione
CAS NO:756499-83-9
Molecular Formula:
Molecular Weight: 388.466
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: 1-(10,10-dimethyl-2-oxo-3-phenyl-3,4-diazatricyclo[5.2.1.0^1,5]dec-4-yl)-2-phenylethane-1,2-dione(CAS DataBase Reference)
NIST Chemistry Reference: 1-(10,10-dimethyl-2-oxo-3-phenyl-3,4-diazatricyclo[5.2.1.0^1,5]dec-4-yl)-2-phenylethane-1,2-dione(756499-83-9)
EPA Substance Registry System: 1-(10,10-dimethyl-2-oxo-3-phenyl-3,4-diazatricyclo[5.2.1.0^1,5]dec-4-yl)-2-phenylethane-1,2-dione(756499-83-9)

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: 756499-83-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 756499-83-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,6,4,9 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 756499-83:
(8*7)+(7*5)+(6*6)+(5*4)+(4*9)+(3*9)+(2*8)+(1*3)=229
229 % 10 = 9
So 756499-83-9 is a valid CAS Registry Number.

756499-83-9Upstream product

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756499-83-9Relevant academic research and scientific papers

Highly diastereoselective allylation and reduction of chiral camphor-derived α-ketoamides

Kulkarni, Neelesh A.,Wang, Shy-Guey,Lee, Li-Chen,Tsai, Huei Ru,Venkatesham, Uppala,Chen, Kwunmin

, p. 336 - 346 (2006)

The diastereoselective allylation and reduction of camphor-derived α-ketoamides to give optically enriched α-hydroxyl amides with high to excellent stereoselectivities are described. Allylation was carried out using allyltributylstannane in the presence o

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