Cas 508168-95-4,(-)-(2R,6S)-1-((1R,2S)-trans-2-(1-methyl-1-phenylethyl)cyclohexyloxycarbonyl)-6-methyl-2-propylpiperidine

508168-95-4

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Basic information

Product Name: (-)-(2R,6S)-1-((1R,2S)-trans-2-(1-methyl-1-phenylethyl)cyclohexyloxycarbonyl)-6-methyl-2-propylpiperidine
Synonyms:
CAS NO:508168-95-4
Molecular Formula:
Molecular Weight: 385.59
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: (-)-(2R,6S)-1-((1R,2S)-trans-2-(1-methyl-1-phenylethyl)cyclohexyloxycarbonyl)-6-methyl-2-propylpiperidine(CAS DataBase Reference)
NIST Chemistry Reference: (-)-(2R,6S)-1-((1R,2S)-trans-2-(1-methyl-1-phenylethyl)cyclohexyloxycarbonyl)-6-methyl-2-propylpiperidine(508168-95-4)
EPA Substance Registry System: (-)-(2R,6S)-1-((1R,2S)-trans-2-(1-methyl-1-phenylethyl)cyclohexyloxycarbonyl)-6-methyl-2-propylpiperidine(508168-95-4)

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: 508168-95-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 508168-95-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,8,1,6 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 508168-95:
(8*5)+(7*0)+(6*8)+(5*1)+(4*6)+(3*8)+(2*9)+(1*5)=164
164 % 10 = 4
So 508168-95-4 is a valid CAS Registry Number.

508168-95-4Upstream product

75-16-1 methylmagnesium bromide

508168-95-4Downstream Products

508168-95-4Relevant academic research and scientific papers

Enantiocontrolled synthesis of 2,6-disubstituted piperidines by desymmetrization of meso-η-(3,4,5)-dihydropyridinylmolybdenum complexes. Application to the total synthesis of (-)-dihydropinidine and (-)-andrachcinidine

Shu, Chutian,Liebeskind, Lanny S.

, p. 2878 - 2879 (2003)

A conceptually new approach to the enantiocontrolled synthesis of 2,6-disubstituted piperidines was achieved by desymmetrization of meso-2,6-dimethoxy-η-(3,4,5)-dihydropyridinylmolybdenum complexes. After protection of the piperidine nitrogen as a urethan

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