Cas 444667-38-3,2-Methylene-3-oxo-butyric acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester

444667-38-3

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Basic information

Product Name: 2-Methylene-3-oxo-butyric acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester
Synonyms: 2-Methylene-3-oxo-butyric acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester
CAS NO:444667-38-3
Molecular Formula:
Molecular Weight: 328.452
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: 2-Methylene-3-oxo-butyric acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-Methylene-3-oxo-butyric acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester(444667-38-3)
EPA Substance Registry System: 2-Methylene-3-oxo-butyric acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester(444667-38-3)

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: 444667-38-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 444667-38-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,4,6,6 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 444667-38:
(8*4)+(7*4)+(6*4)+(5*6)+(4*6)+(3*7)+(2*3)+(1*8)=173
173 % 10 = 3
So 444667-38-3 is a valid CAS Registry Number.

444667-38-3Upstream product

192199-24-9 (1R,3R,4S)-8-phenylmenthyl 2-methylacetoacetate

444667-38-3Downstream Products

444667-38-3Relevant academic research and scientific papers

Diastereoselective aziridination of chiral α-carbonyl enoates

Fioravanti, Stefania,Morreale, Alberto,Pellacani, Lucio,Tardella, Paolo A.

, p. 4972 - 4974 (2002)

Nosyloxycarbamates very efficiently aziridinate optically active α-carbonyl enoates with high levels of diastereoselectivity under mild conditions and in a straight-forward process.

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