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CAS

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183903-04-0

(+)-γ-cyclohomocitral is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 183903-04-0 Structure

  • Basic information

    1. Product Name: (+)-γ-cyclohomocitral
    2. Synonyms: (+)-γ-cyclohomocitral
    3. CAS NO:183903-04-0
    4. Molecular Formula:
    5. Molecular Weight: 166.263
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 183903-04-0.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: (+)-γ-cyclohomocitral(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+)-γ-cyclohomocitral(183903-04-0)
    11. EPA Substance Registry System: (+)-γ-cyclohomocitral(183903-04-0)

  • 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: 183903-04-0(Hazardous Substances Data)

183903-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183903-04-0 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 183903-04:
(8*1)+(7*8)+(6*3)+(5*9)+(4*0)+(3*3)+(2*0)+(1*4)=140
140 % 10 = 0
So 183903-04-0 is a valid CAS Registry Number.

183903-04-0Relevant articles and documents

First total synthesis and assignment of the stereochemistry of crispatenine

Bourdron, Julien,Commeiras, Laurent,Audran, Gerard,Vanthuyne, Nicolas,Hubaud,Parrain, Jean-Luc

, p. 3770 - 3775 (2008/02/04)

(Figure Presented) The first racemic and enantioselective synthesis of crispatenine 1 has been achieved, which involved a few steps, enabling the assignment of the absolute and relative configurations.

First enantioselective synthesis and determination of the absolute configuration of natural (+)-dehydro-β-monocyclonerolidol

Palombo, Elie,Audran, G.érard,Monti, Honoré

, p. 6463 - 6464 (2007/10/03)

The enantioselective synthesis and determination of the absolute configuration of (+)-dehydro-β-monocyclonerolidol, a natural product isolated from the liverwort P. subobtusa, has been achieved starting from (+)-karahana lactone as an enantiopure building

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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