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66917-82-6

2-Decen-4-one, 2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 66917-82-6 Structure

  • Basic information

    1. Product Name: 2-Decen-4-one, 2-methyl-
    2. Synonyms:
    3. CAS NO:66917-82-6
    4. Molecular Formula: C11H20O
    5. Molecular Weight: 168.279
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 66917-82-6.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: 2-Decen-4-one, 2-methyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Decen-4-one, 2-methyl-(66917-82-6)
    11. EPA Substance Registry System: 2-Decen-4-one, 2-methyl-(66917-82-6)

  • 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: 66917-82-6(Hazardous Substances Data)

66917-82-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66917-82-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,9,1 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 66917-82:
(7*6)+(6*6)+(5*9)+(4*1)+(3*7)+(2*8)+(1*2)=166
166 % 10 = 6
So 66917-82-6 is a valid CAS Registry Number.

66917-82-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-2-decen-4-one

1.2 Other means of identification

Product number -
Other names 2-methyldec-2-en-4-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:66917-82-6 SDS

66917-82-6Downstream Products

66917-82-6Relevant articles and documents

Factors controlling the equilibrium of Pt-catalyzed [1,2]- versus [1,3]-acyloxy migration

Cho, Eun Jin

supporting information; experimental part, p. 4495 - 4498 (2012/05/04)

Pick a pathway: Upon activation with an electrophilic transition-metal catalyst, a propargylic acetate undergoes competing [1,2]- and [1,3]-acyloxy migration depending on the reaction temperature as well as the substituent pattern around the alkyne. The nature of the catalyst also affects the reaction course. The reactions provided clear evidence for the interconversion between carbenoid and allene intermediates (see scheme).

Synthesis of aliphatic ketones from allylic alcohols through consecutive isomerization and chelation-assisted hydroacylation by a rhodium catalyst

Lee, Dae-Yon,Moon, Choong Woon,Jun, Chul-Ho

, p. 3945 - 3948 (2007/10/03)

Abstract: An allylic alcohol, utilized as a precursor for an aliphatic aldehyde, reacted with olefins to afford aliphatic ketones in the presence of RhCl(PPh3)3, 2-amino-4-picoline, aniline, and benzoic acid through a tandem reaction of an isomerization and a chelation-assisted hydroacylation.

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