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CAS

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183903-01-7

(1'R,3'R)-2-(3'-hydroxy-2',2'-dimethyl-6'-methylene-cyclohexyl)-ethyl trimethylacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 183903-01-7 Structure

  • Basic information

    1. Product Name: (1'R,3'R)-2-(3'-hydroxy-2',2'-dimethyl-6'-methylene-cyclohexyl)-ethyl trimethylacetate
    2. Synonyms: (1'R,3'R)-2-(3'-hydroxy-2',2'-dimethyl-6'-methylene-cyclohexyl)-ethyl trimethylacetate
    3. CAS NO:183903-01-7
    4. Molecular Formula:
    5. Molecular Weight: 268.397
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 183903-01-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (1'R,3'R)-2-(3'-hydroxy-2',2'-dimethyl-6'-methylene-cyclohexyl)-ethyl trimethylacetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1'R,3'R)-2-(3'-hydroxy-2',2'-dimethyl-6'-methylene-cyclohexyl)-ethyl trimethylacetate(183903-01-7)
    11. EPA Substance Registry System: (1'R,3'R)-2-(3'-hydroxy-2',2'-dimethyl-6'-methylene-cyclohexyl)-ethyl trimethylacetate(183903-01-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 183903-01-7(Hazardous Substances Data)

183903-01-7 Usage

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

183903-01-7Relevant articles and documents

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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