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116531-33-0

Cyclohexanol, 3-methyl-, acetate, cis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 116531-33-0 Structure

  • Basic information

    1. Product Name: Cyclohexanol, 3-methyl-, acetate, cis-
    2. Synonyms:
    3. CAS NO:116531-33-0
    4. Molecular Formula: C9H16O2
    5. Molecular Weight: 156.225
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 116531-33-0.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: Cyclohexanol, 3-methyl-, acetate, cis-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexanol, 3-methyl-, acetate, cis-(116531-33-0)
    11. EPA Substance Registry System: Cyclohexanol, 3-methyl-, acetate, cis-(116531-33-0)

  • 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: 116531-33-0(Hazardous Substances Data)

116531-33-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116531-33-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,5,3 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 116531-33:
(8*1)+(7*1)+(6*6)+(5*5)+(4*3)+(3*1)+(2*3)+(1*3)=100
100 % 10 = 0
So 116531-33-0 is a valid CAS Registry Number.

116531-33-0Downstream Products

116531-33-0Relevant articles and documents

NEW METHODS FOR HYDRODEALKENYLATION

-

Paragraph 00030; 00032-00033, (2022/01/24)

The present disclosure pertains to new methods of performing a hydrodealkenylation of monounsaturated alcohols, thiols, and derivatives thereof, such as terpenes and derivatives, comprising ozonolysis and quenching using a sulfinic acid or sulfinic acid salt.

Palladium-Catalyzed C-Alkylations of the Highly Acidic and Enolic Triacetic Acid Lactone. Mechanism and Stereochemistry

Moreno-Manas, Marcial,Ribas, Jordi,Virgili, Albert

, p. 5328 - 5335 (2007/10/02)

4-Hydroxy-6-methyl-2-pyrone (triacetic acid lactone) (1) is efficiently alkylated at C-3 with primary and secondary allylic substrates under thermodynamic control by using palladium(0) catalysts.Controlled hydrogenation of the resulting allylated derivatives affords pyrones with saturated chains at C-3.Allylic alkylations occur with retention of configuration at the allylic center, probably through a reversible kinetically favored O-alkylation.

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