Cas 116044-16-7,(1'R,2'S,5'R)-2'-(1-methyl-1-phenylethyl)-5'-methylcyclohexyl 3,5-dinitrobenzoate

116044-16-7

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Basic information

Product Name: (1'R,2'S,5'R)-2'-(1-methyl-1-phenylethyl)-5'-methylcyclohexyl 3,5-dinitrobenzoate
Synonyms: (1'R,2'S,5'R)-2'-(1-methyl-1-phenylethyl)-5'-methylcyclohexyl 3,5-dinitrobenzoate
CAS NO:116044-16-7
Molecular Formula:
Molecular Weight: 426.469
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: (1'R,2'S,5'R)-2'-(1-methyl-1-phenylethyl)-5'-methylcyclohexyl 3,5-dinitrobenzoate(CAS DataBase Reference)
NIST Chemistry Reference: (1'R,2'S,5'R)-2'-(1-methyl-1-phenylethyl)-5'-methylcyclohexyl 3,5-dinitrobenzoate(116044-16-7)
EPA Substance Registry System: (1'R,2'S,5'R)-2'-(1-methyl-1-phenylethyl)-5'-methylcyclohexyl 3,5-dinitrobenzoate(116044-16-7)

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: 116044-16-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 116044-16-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,0,4 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 116044-16:
(8*1)+(7*1)+(6*6)+(5*0)+(4*4)+(3*4)+(2*1)+(1*6)=87
87 % 10 = 7
So 116044-16-7 is a valid CAS Registry Number.

116044-16-7Upstream product

116044-16-7Downstream Products

116044-16-7Relevant academic research and scientific papers

Synthesis and characterization of all stereoisomers of 8-phenylmenthol

Fernandez, Franco,Garcia-Mera, Xerardo,Lopez, Carmen,Rodriguez, Gonzalo,Rodriguez-Borges, Jose Enrique

, p. 4805 - 4815 (2000)

New, improved and/or specific syntheses of the diastereoisomers of (-)-8-phenylmenthol are described. The configurations of these products, usable as chiral auxiliaries, were confirmed by X-ray diffractometry of their 3,5-dinitrobenzoates.

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