Cas 1027313-50-3,(1R,2R,5R)-3-[(E)-(R)-1-Furan-2-yl-2-(4-methoxy-phenyl)-ethylimino]-2,6,6-trimethyl-bicyclo[3.1.1]heptan-2-ol

1027313-50-3

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Basic information

Product Name: (1R,2R,5R)-3-[(E)-(R)-1-Furan-2-yl-2-(4-methoxy-phenyl)-ethylimino]-2,6,6-trimethyl-bicyclo[3.1.1]heptan-2-ol
Synonyms: (1R,2R,5R)-3-[(E)-(R)-1-Furan-2-yl-2-(4-methoxy-phenyl)-ethylimino]-2,6,6-trimethyl-bicyclo[3.1.1]heptan-2-ol
CAS NO:1027313-50-3
Molecular Formula:
Molecular Weight: 367.488
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: (1R,2R,5R)-3-[(E)-(R)-1-Furan-2-yl-2-(4-methoxy-phenyl)-ethylimino]-2,6,6-trimethyl-bicyclo[3.1.1]heptan-2-ol(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2R,5R)-3-[(E)-(R)-1-Furan-2-yl-2-(4-methoxy-phenyl)-ethylimino]-2,6,6-trimethyl-bicyclo[3.1.1]heptan-2-ol(1027313-50-3)
EPA Substance Registry System: (1R,2R,5R)-3-[(E)-(R)-1-Furan-2-yl-2-(4-methoxy-phenyl)-ethylimino]-2,6,6-trimethyl-bicyclo[3.1.1]heptan-2-ol(1027313-50-3)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1027313-50-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1027313-50-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,3,1 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1027313-50:
(9*1)+(8*0)+(7*2)+(6*7)+(5*3)+(4*1)+(3*3)+(2*5)+(1*0)=103
103 % 10 = 3
So 1027313-50-3 is a valid CAS Registry Number.

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1027313-50-3Relevant academic research and scientific papers

Asymmetric synthesis. XVIII. Stereocontrolled synthesis of α-substituted-2-furfurylamines via chiral intermediates

Shikui,Aiqiao,Lanjun,Yaozhong

, p. 2485 - 2488 (2007/10/02)

The stereocontrolled synthesis of (R)-α-alkyl-2-furfurylamines (5), using (-)-2-hydroxypinan-3-one as a chiral auxiliary, had been studied. The e.e. values of (5) were 91.4->98%, which determined by capillary GC (stationary phase: Chirasil-Val).

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