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CAS

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25094-54-6

2-(3-methylcyclohex-3-en-1-yl)propan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 25094-54-6 Structure

  • Basic information

    1. Product Name: 2-(3-methylcyclohex-3-en-1-yl)propan-2-ol
    2. Synonyms: 2-(3-Methylcyclohex-3-en-1-yl)propan-2-ol; 3-cyclohexene-1-methanol, α,α,3-trimethyl-
    3. CAS NO:25094-54-6
    4. Molecular Formula: C10H18O
    5. Molecular Weight: 154.2493
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 25094-54-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 210.7°C at 760 mmHg
    3. Flash Point: 79°C
    4. Appearance: N/A
    5. Density: 0.934g/cm3
    6. Vapor Pressure: 0.0432mmHg at 25°C
    7. Refractive Index: 1.482
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-(3-methylcyclohex-3-en-1-yl)propan-2-ol(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(3-methylcyclohex-3-en-1-yl)propan-2-ol(25094-54-6)
    12. EPA Substance Registry System: 2-(3-methylcyclohex-3-en-1-yl)propan-2-ol(25094-54-6)

  • 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: 25094-54-6(Hazardous Substances Data)

25094-54-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25094-54-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,0,9 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 25094-54:
(7*2)+(6*5)+(5*0)+(4*9)+(3*4)+(2*5)+(1*4)=106
106 % 10 = 6
So 25094-54-6 is a valid CAS Registry Number.

25094-54-6Relevant articles and documents

ALIPHATIC CLAISEN REARRANGEMENT PROMOTED BY ORGANOALUMINIUM REAGENTS.

Takai,Mori,Oshima,Nozaki

, p. 446 - 451 (2007/10/02)

Organoaluminium compounds, R//3Al, promote the Claisen rearrangement of allyl vinyl ether derivatives at room temperature under transfer of R or H as a nucleophile to the aldehydic carbon. Treatment of 1-butyl-2-propenyl vinyl ether with a hexane solution of Me//3Al (1. 0 M, 2. 2 equiv) in CH//2ClCH//2Cl at 25 degree C afforded 5-decen-2-ol (91% yield, E/Z equals 47/53), which was produced by the left bracket 3,3 right bracket sigmatropic rearrangement and successive methylation. The rearrangements with alkynylation, alkenylation, and hydrogenation are also achieved. The regular Claisen rearrangement products, of gamma , delta -unsaturated aldehydes (ketones), are obtained at 25 degree C in good to excellent yields with Et//2AlSPh (2. 5 equiv) or the combination of Et//2AlCl (2. 0 euiv) and PPh//3 (2. 2 equiv).

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