Cas 945859-13-2,(1S,1'S)-7,7-dimethylbicyclo[2.2.1]heptane-1-N-(1'-phenyl)ethylcarboxylamide-2-one

945859-13-2

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Basic information

Product Name: (1S,1'S)-7,7-dimethylbicyclo[2.2.1]heptane-1-N-(1'-phenyl)ethylcarboxylamide-2-one
Synonyms:
CAS NO:945859-13-2
Molecular Formula:
Molecular Weight: 285.386
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: (1S,1'S)-7,7-dimethylbicyclo[2.2.1]heptane-1-N-(1'-phenyl)ethylcarboxylamide-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (1S,1'S)-7,7-dimethylbicyclo[2.2.1]heptane-1-N-(1'-phenyl)ethylcarboxylamide-2-one(945859-13-2)
EPA Substance Registry System: (1S,1'S)-7,7-dimethylbicyclo[2.2.1]heptane-1-N-(1'-phenyl)ethylcarboxylamide-2-one(945859-13-2)

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: 945859-13-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 945859-13-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,8,5 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 945859-13:
(8*9)+(7*4)+(6*5)+(5*8)+(4*5)+(3*9)+(2*1)+(1*3)=222
222 % 10 = 2
So 945859-13-2 is a valid CAS Registry Number.

945859-13-2Upstream product

945859-13-2Downstream Products

1161442-50-7 C₂₅H₃₀N₂O

945859-13-2Relevant academic research and scientific papers

Synthesis of novel chiral Schiff bases and their application in asymmetric transfer hydrogenation of prochiral ketones

Zhou, Zhongqiang,Bian, Yongjun

experimental part, p. 682 - 687 (2010/11/04)

Novel chiral Schiff bases were synthesized from (+)-camphor, and their application to asymmetric transfer hydrogenation of prochiral ketones is described. The asymmetric transfer hydrogenation reaction could afford excellent conversion rates (up to 97.3%) and up to 27.3% enantiomeric excess.

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