Cas 872865-10-6,Bicyclo[2.2.1]heptane-1-carboxamide, N-[(1S)-2-hydroxy-1-phenylethyl]-7,7-dimethyl-2-oxo-, (1S,4R)-

872865-10-6

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Basic information

Product Name: Bicyclo[2.2.1]heptane-1-carboxamide, N-[(1S)-2-hydroxy-1-phenylethyl]-7,7-dimethyl-2-oxo-, (1S,4R)-
Synonyms:
CAS NO:872865-10-6
Molecular Formula: C18H23NO3
Molecular Weight: 301.38000
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: Bicyclo[2.2.1]heptane-1-carboxamide, N-[(1S)-2-hydroxy-1-phenylethyl]-7,7-dimethyl-2-oxo-, (1S,4R)-(CAS DataBase Reference)
NIST Chemistry Reference: Bicyclo[2.2.1]heptane-1-carboxamide, N-[(1S)-2-hydroxy-1-phenylethyl]-7,7-dimethyl-2-oxo-, (1S,4R)-(872865-10-6)
EPA Substance Registry System: Bicyclo[2.2.1]heptane-1-carboxamide, N-[(1S)-2-hydroxy-1-phenylethyl]-7,7-dimethyl-2-oxo-, (1S,4R)-(872865-10-6)

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: 872865-10-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 872865-10-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,2,8,6 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 872865-10:
(8*8)+(7*7)+(6*2)+(5*8)+(4*6)+(3*5)+(2*1)+(1*0)=206
206 % 10 = 6
So 872865-10-6 is a valid CAS Registry Number.

872865-10-6Upstream product

872865-10-6Downstream Products

1000304-15-3 C₁₈H₂₁NO₂

872865-10-6Relevant academic research and scientific papers

New chiral hydroxyoxazolines based on ketopinic acid and their use in the asymmetric Diels-Alder reaction

Barroso, Santiago,Blay, Gonzalo,Cardona, Luz,Pedro, José R.

, p. 2659 - 2662 (2008/02/13)

Several chiral hydroxyoxazolines have been prepared starting from (1S)-(+)-ketopinic acid and enantiopure β-amino alcohols by short synthetic routes. They have been employed in the catalytic asymmetric Diels-Alder reaction, resulting in ee values of up to

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