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CAS

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1344731-03-8

(R)-4-methyl-4-(4-methylpent-3-en-1-yl)cyclohex-2-en-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1344731-03-8 Structure

  • Basic information

    1. Product Name: (R)-4-methyl-4-(4-methylpent-3-en-1-yl)cyclohex-2-en-1-one
    2. Synonyms: (R)-4-methyl-4-(4-methylpent-3-en-1-yl)cyclohex-2-en-1-one
    3. CAS NO:1344731-03-8
    4. Molecular Formula:
    5. Molecular Weight: 192.301
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1344731-03-8.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: (R)-4-methyl-4-(4-methylpent-3-en-1-yl)cyclohex-2-en-1-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-4-methyl-4-(4-methylpent-3-en-1-yl)cyclohex-2-en-1-one(1344731-03-8)
    11. EPA Substance Registry System: (R)-4-methyl-4-(4-methylpent-3-en-1-yl)cyclohex-2-en-1-one(1344731-03-8)

  • 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: 1344731-03-8(Hazardous Substances Data)

1344731-03-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1344731-03-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,4,7,3 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1344731-03:
(9*1)+(8*3)+(7*4)+(6*4)+(5*7)+(4*3)+(3*1)+(2*0)+(1*3)=138
138 % 10 = 8
So 1344731-03-8 is a valid CAS Registry Number.

1344731-03-8Downstream Products

1344731-03-8Relevant articles and documents

Enantioselective Conversion of Achiral Cyclohexadienones to Chiral Cyclohexenones by Desymmetrization

Han, Yixin,Breitler, Simon,Zheng, Shao-Liang,Corey

, p. 6172 - 6175 (2016)

The enantioselective reduction of prochiral 4,4-disubstituted 2,5-cyclohexadienones to chiral 2-cyclohexenones has been accomplished by the use of a carefully selected chiral bisphosphine-CuI complex and diisobutylaluminum hydride-hexamethylphosphoric triamide complex. This reagent has provided access to a key bicyclic intermediate for the total synthesis of the natural enantiomer of the pentacyclic sesterterpene retigeranic acid that involves spatial discrimination between CH3 and CH2CH2R substituents, an operation that has been elusive previously. In addition, a second method for desymmetrization is described using catalytic enantioselective [4 + 2]-cycloaddition of cyclopentadiene to prochiral 4,4-disubstituted 2,5-cyclohexadienones.

Stereoselective alkylation of allylic alcohols: Tandem ethylation and functionalization

Das, Pragna Pratic,Lysenko, Ivan L.,Cha, Jin Kun

supporting information; experimental part, p. 9459 - 9461 (2011/11/07)

A versatile formal SN2 alkylation of allylic alcohols has been devised by means of the Kulinkovich reagent and in situ elaboration of the presumed alkyltitanium intermediates with electrophiles (see scheme). The utility of this method has been

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