Cas 945656-33-7,(4S,5R)-4-[(1R,2S,5R)-(-)-menthyloxycarbonyl]-5-(1-naphthyl)-2-phenyl-4,5-dihydrooxazole

945656-33-7

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Basic information

Product Name: (4S,5R)-4-[(1R,2S,5R)-(-)-menthyloxycarbonyl]-5-(1-naphthyl)-2-phenyl-4,5-dihydrooxazole
Synonyms:
CAS NO:945656-33-7
Molecular Formula:
Molecular Weight: 455.597
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: (4S,5R)-4-[(1R,2S,5R)-(-)-menthyloxycarbonyl]-5-(1-naphthyl)-2-phenyl-4,5-dihydrooxazole(CAS DataBase Reference)
NIST Chemistry Reference: (4S,5R)-4-[(1R,2S,5R)-(-)-menthyloxycarbonyl]-5-(1-naphthyl)-2-phenyl-4,5-dihydrooxazole(945656-33-7)
EPA Substance Registry System: (4S,5R)-4-[(1R,2S,5R)-(-)-menthyloxycarbonyl]-5-(1-naphthyl)-2-phenyl-4,5-dihydrooxazole(945656-33-7)

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: 945656-33-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 945656-33-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,5,6,5 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 945656-33:
(8*9)+(7*4)+(6*5)+(5*6)+(4*5)+(3*6)+(2*3)+(1*3)=207
207 % 10 = 7
So 945656-33-7 is a valid CAS Registry Number.

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945656-33-7Relevant academic research and scientific papers

Asymmetric cyclization reactions of N-benzoyl-α-dehydroarylalanine alkyl esters via photoinduced electron transfer from achiral and chiral amines

Sasaki, Yuji,Watanabe, Haruo,Igarashi, Tetsutaro,Sakurai, Tadamitsu

, p. 1329 - 1353 (2011/07/30)

Irradiation of the title compounds [(Z)-1] having (S)-(+)-sec-butyl, (-)- menthyl, and related chiral auxiliaries in methanol and 1,2-dichloroethane containing 2-(diethylamino)ethanol afforded chiral auxiliary-substituted (4S,5S)-, (4R,5R)-, (4R,5S)-, and

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