Cas 1563207-96-4,benzyl (S)-N-[((1S,2S,3R,5S)-2-hydroxy-2,6,6-trimethylbicyclo[3.1.1]hept-3-ylamino)-3-methyl-1-oxobut-2-yl]carbamate

1563207-96-4

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Basic information

Product Name: benzyl (S)-N-[((1S,2S,3R,5S)-2-hydroxy-2,6,6-trimethylbicyclo[3.1.1]hept-3-ylamino)-3-methyl-1-oxobut-2-yl]carbamate
Synonyms: benzyl (S)-N-[((1S,2S,3R,5S)-2-hydroxy-2,6,6-trimethylbicyclo[3.1.1]hept-3-ylamino)-3-methyl-1-oxobut-2-yl]carbamate
CAS NO:1563207-96-4
Molecular Formula:
Molecular Weight: 402.534
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 (S)-N-[((1S,2S,3R,5S)-2-hydroxy-2,6,6-trimethylbicyclo[3.1.1]hept-3-ylamino)-3-methyl-1-oxobut-2-yl]carbamate(CAS DataBase Reference)
NIST Chemistry Reference: benzyl (S)-N-[((1S,2S,3R,5S)-2-hydroxy-2,6,6-trimethylbicyclo[3.1.1]hept-3-ylamino)-3-methyl-1-oxobut-2-yl]carbamate(1563207-96-4)
EPA Substance Registry System: benzyl (S)-N-[((1S,2S,3R,5S)-2-hydroxy-2,6,6-trimethylbicyclo[3.1.1]hept-3-ylamino)-3-methyl-1-oxobut-2-yl]carbamate(1563207-96-4)

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: 1563207-96-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1563207-96-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,3,2,0 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1563207-96:
(9*1)+(8*5)+(7*6)+(6*3)+(5*2)+(4*0)+(3*7)+(2*9)+(1*6)=164
164 % 10 = 4
So 1563207-96-4 is a valid CAS Registry Number.

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1563207-96-4Relevant academic research and scientific papers

Organocatalysis of asymmetric aldol reaction in water: Comparison of catalytic properties of (S)-valine and (S)-proline amides

Kucherenko,Siyutkin,Dashkin,Zlotin

, p. 1010 - 1015 (2014/03/21)

(S)-Valine amides containing (S)- or (R)-α-phenylethyl substituents at N1 atom efficiently catalyze asymmetric aldol reactions between cyclic (heterocyclic) ketones and aromatic aldehydes in water, predominantly giving rise to the aldol anti-di

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