Cas 183903-01-7,(1'R,3'R)-2-(3'-hydroxy-2',2'-dimethyl-6'-methylene-cyclohexyl)-ethyl trimethylacetate

183903-01-7

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Basic information

Product Name: (1'R,3'R)-2-(3'-hydroxy-2',2'-dimethyl-6'-methylene-cyclohexyl)-ethyl trimethylacetate
Synonyms: (1'R,3'R)-2-(3'-hydroxy-2',2'-dimethyl-6'-methylene-cyclohexyl)-ethyl trimethylacetate
CAS NO:183903-01-7
Molecular Formula:
Molecular Weight: 268.397
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,3'R)-2-(3'-hydroxy-2',2'-dimethyl-6'-methylene-cyclohexyl)-ethyl trimethylacetate(CAS DataBase Reference)
NIST Chemistry Reference: (1'R,3'R)-2-(3'-hydroxy-2',2'-dimethyl-6'-methylene-cyclohexyl)-ethyl trimethylacetate(183903-01-7)
EPA Substance Registry System: (1'R,3'R)-2-(3'-hydroxy-2',2'-dimethyl-6'-methylene-cyclohexyl)-ethyl trimethylacetate(183903-01-7)

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: 183903-01-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 183903-01-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,9,0 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 183903-01:
(8*1)+(7*8)+(6*3)+(5*9)+(4*0)+(3*3)+(2*0)+(1*1)=137
137 % 10 = 7
So 183903-01-7 is a valid CAS Registry Number.

183903-01-7Upstream product

183903-01-7Downstream Products

183903-01-7Relevant academic research and scientific papers

Enantioselective synthesis of γ-cyclohomocitral, pallescensone, and ancistrodial

Vidari, Giovanni,Lanfranchi, Gianluigi,Masciaga, Francesca,Moriggi, Jean-Dominique

, p. 3009 - 3020 (2007/10/03)

A simple and efficient enantioselective synthesis of γ-cyclohomocitral, a key and versatile intermediate for the synthesis of some monocyclofarnesane terpenoids, is described. This features a highly sitoselective Sharpless asymmetric dihydroxylation of a

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