Cas 910545-75-4,(E,1R,3R,4S)-3-allyl-3-(benzylideneamino)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one

910545-75-4

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Basic information

Product Name: (E,1R,3R,4S)-3-allyl-3-(benzylideneamino)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
Synonyms: (E,1R,3R,4S)-3-allyl-3-(benzylideneamino)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
CAS NO:910545-75-4
Molecular Formula:
Molecular Weight: 295.425
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: (E,1R,3R,4S)-3-allyl-3-(benzylideneamino)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (E,1R,3R,4S)-3-allyl-3-(benzylideneamino)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one(910545-75-4)
EPA Substance Registry System: (E,1R,3R,4S)-3-allyl-3-(benzylideneamino)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one(910545-75-4)

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: 910545-75-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 910545-75-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,0,5,4 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 910545-75:
(8*9)+(7*1)+(6*0)+(5*5)+(4*4)+(3*5)+(2*7)+(1*5)=154
154 % 10 = 4
So 910545-75-4 is a valid CAS Registry Number.

910545-75-4Upstream product

910545-75-4Downstream Products

910545-75-4Relevant academic research and scientific papers

Enantioselective transfer aminoallylation: Synthesis of optically active homoallylic primary amines

Sugiura, Masaharu,Mori, Chieko,Kobayashi, Shu

, p. 11038 - 11039 (2006)

A camphorquinone-derived chiral homoallylic amine was found to react with various aldehydes via imine formation and asymmetric 2-azonia-Cope rearrangement to give optically active homoallylic primary amines. A practical level of enantioselectivity with hi

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