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5951-61-1

(+/-)-β-Cadinene is a bicyclic sesquiterpene hydrocarbon, a class of organic compounds derived from isoprene units, with the molecular formula C15H24. It is an optically active compound, meaning it exists in two enantiomeric forms, (+) and (-), which are mirror images of each other. This organic compound is widely found in various essential oils, particularly in plants from the Lamiaceae and Lauraceae families, and is known for its woody, earthy aroma. It is used in the fragrance industry and as a precursor in the synthesis of other chemicals. Due to its chiral nature, (+/-)-β-cadinene can be separated into its individual enantiomers, which may exhibit different biological activities or fragrance properties.

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  • 5951-61-1 Structure

  • Basic information

    1. Product Name: (+/-)-β-cadinene
    2. Synonyms:
    3. CAS NO:5951-61-1
    4. Molecular Formula:
    5. Molecular Weight: 204.356
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5951-61-1.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: (+/-)-β-cadinene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+/-)-β-cadinene(5951-61-1)
    11. EPA Substance Registry System: (+/-)-β-cadinene(5951-61-1)

  • 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: 5951-61-1(Hazardous Substances Data)

5951-61-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5951-61-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,5 and 1 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5951-61:
(6*5)+(5*9)+(4*5)+(3*1)+(2*6)+(1*1)=111
111 % 10 = 1
So 5951-61-1 is a valid CAS Registry Number.

5951-61-1Downstream Products

5951-61-1Relevant articles and documents

The role of germacrene D as a precursor in sesquiterpene biosynthesis: Investigations of acid catalyzed, photochemically and thermally induced rearrangements

Buelow, Nils,Koenig, Wilfried A

, p. 141 - 168 (2007/10/03)

Germacrene D is considered as a precursor of many sesquiterpene hydrocarbons. We have investigated the acid catalyzed as well as the photochemically and thermally induced rearrangement processes of germacrene D isolated from several Solidago species, which contain both enantiomers of germacrene D. Enantiomeric mixtures of sesquiterpenes of the cadinane, eudesmane (selinane), oppositane, axane, isodaucane, and bourbonane group as well as isogermacrene D were identified as main products and made available as reference compounds for structure investigations and stereochemical assignments of plant constituents. δ-Amorphene, one of the rearrangement products, was identified as a natural product for the first time. The absolute configuration of γ-amorphene was revised by correlation with the absolute configuration of germacrene D. The mechanisms of the rearrangement reactions are discussed. (C) 2000 Elsevier Science Ltd.

DIASTEREOSELECTIVE SYNTHESIS OF β- AND γ2-MUUROLENE: A CARBOCATIONIC PATHWAY FROM MONO- TO SESQUITERPENES

Azizur-Rahman,Klein, Herbert,Dressel, Juergen,Mayr, Herbert

, p. 6041 - 6046 (2007/10/02)

The Lewis acid catalysed addition of the piperityl chlorides 6 to isoprene yields adduct 7, which undergoes a cis-stereoselective cyclisation to give the diastereoisomeric muurolene monohydrochlorides 8.Treatment with potassium tert-butoxide affords β- an

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