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135616-12-5

(R)-methyl 4-(1-methylethyl)-2-oxocyclohexane-6-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 135616-12-5 Structure

  • Basic information

    1. Product Name: (R)-methyl 4-(1-methylethyl)-2-oxocyclohexane-6-carboxylate
    2. Synonyms: (R)-methyl 4-(1-methylethyl)-2-oxocyclohexane-6-carboxylate
    3. CAS NO:135616-12-5
    4. Molecular Formula:
    5. Molecular Weight: 198.262
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 135616-12-5.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)-methyl 4-(1-methylethyl)-2-oxocyclohexane-6-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-methyl 4-(1-methylethyl)-2-oxocyclohexane-6-carboxylate(135616-12-5)
    11. EPA Substance Registry System: (R)-methyl 4-(1-methylethyl)-2-oxocyclohexane-6-carboxylate(135616-12-5)

  • 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: 135616-12-5(Hazardous Substances Data)

135616-12-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135616-12-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,6,1 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 135616-12:
(8*1)+(7*3)+(6*5)+(5*6)+(4*1)+(3*6)+(2*1)+(1*2)=115
115 % 10 = 5
So 135616-12-5 is a valid CAS Registry Number.

135616-12-5Relevant articles and documents

Stereochemical Insights into the Anaerobic Degradation of 4-Isopropylbenzoyl-CoA in the Denitrifying Bacterium Strain pCyN1

Küppers, Julian,Becker, Patrick,Jarling, René,D?rries, Marvin,Caki?, Nevenka,Schmidtmann, Marc,Christoffers, Jens,Rabus, Ralf,Wilkes, Heinz

, p. 4722 - 4731 (2019)

The constitutions and absolute configurations of two previously unknown intermediates, (1S,2S,4S)-2-hydroxy-4-isopropylcyclohexane-1-carboxylate and (S)-3-isopropylpimelate, of anaerobic degradation of p-cymene in the bacterium Aromatoleum aromaticum pCyN

Regioselective Conversion of Cycloalkanones to Vinyl Bromide with 1,2-Functionality Transposition. A General Strategem

Paquette, Leo A.,Dahnke, Karl,Doyon, Julien,He, Wei,Wyant, Kenetha,Friedrich, Dirk

, p. 6199 - 6205 (2007/10/02)

Cyclic β-keto esters, available by regioselective acylation of cycloalkanone enolates, are rapidly transformed to α,β-unsaturated acids.This functionality transposition allows the derived 3-hydroxy-4-methylthiazole-2-(3H)-thione derivatives to serve as precursors to synthetically useful vinyl bromides.The process involves heating the hydroxamate ester with AIBN in bromotrichloromethane solution.Alkylative and ring contractive variants of the methodology are highlighted.The short sequence makes available precursors to vinyl anions that are not otherwise conveniently accessible.

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