Welcome to LookChem.com Sign In|Join Free

CAS

  • or

2142-78-1

1-(2,3,4,6-tetramethylphenyl)ethanone, also known as p-menthane-3,8-diol, is a chemical compound with the molecular formula C13H20O. It is a ketone derivative of menthol and is characterized by its pale yellow liquid appearance, minty, woody odor, and cooling, refreshing properties.

2142-78-1 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 2142-78-1 Structure

  • Basic information

    1. Product Name: 1-(2,3,4,6-tetramethylphenyl)ethanone
    2. Synonyms: Acetophenone, 2',3',4',6'-tetramethyl-; Acetylisodurene; Ethanone, 1- (2,3,4,6-tetramethylphenyl)-
    3. CAS NO:2142-78-1
    4. Molecular Formula: C12H16O
    5. Molecular Weight: 176.2548
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2142-78-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 281.9°C at 760 mmHg
    3. Flash Point: 115.9°C
    4. Appearance: N/A
    5. Density: 0.947g/cm3
    6. Vapor Pressure: 0.00346mmHg at 25°C
    7. Refractive Index: 1.509
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-(2,3,4,6-tetramethylphenyl)ethanone(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-(2,3,4,6-tetramethylphenyl)ethanone(2142-78-1)
    12. EPA Substance Registry System: 1-(2,3,4,6-tetramethylphenyl)ethanone(2142-78-1)

  • 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: 2142-78-1(Hazardous Substances Data)

2142-78-1 Usage

Uses

Used in Flavor and Fragrance Industry:
1-(2,3,4,6-tetramethylphenyl)ethanone is used as a flavoring agent and fragrance in various consumer products for its pleasant aroma and cooling sensation.
Used in Perfume Production:
1-(2,3,4,6-tetramethylphenyl)ethanone is used as a key ingredient in the production of perfumes, contributing to their refreshing and long-lasting scents.
Used in Cosmetics and Personal Care Products:
1-(2,3,4,6-tetramethylphenyl)ethanone is used as an additive in cosmetics and personal care products, enhancing their sensory appeal and providing a cooling effect on the skin.
Used in Oral Care Products:
1-(2,3,4,6-tetramethylphenyl)ethanone is used in oral care products for its antimicrobial and anti-inflammatory properties, promoting oral health and freshness.
Used in Skincare Products:
1-(2,3,4,6-tetramethylphenyl)ethanone is used in skincare products for its antimicrobial and anti-inflammatory properties, helping to soothe and protect the skin.

Check Digit Verification of cas no

The CAS Registry Mumber 2142-78-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,4 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2142-78:
(6*2)+(5*1)+(4*4)+(3*2)+(2*7)+(1*8)=61
61 % 10 = 1
So 2142-78-1 is a valid CAS Registry Number.

2142-78-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Acetylisodurene

1.2 Other means of identification

Product number -
Other names acetoisodurene

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:2142-78-1 SDS

2142-78-1Relevant articles and documents

Positional Reactivity of Acylpolymethylbenzenes in Electrophilic Substitution

Matsuura, Kazunori,Kimura, Yasuo,Takahashi, Hisakazu,Morita, Toshio,Takahashi, Ichiro,et al.

, p. 757 - 765 (2007/10/02)

Friedel-Crafts acylation, bromination, deuteration, and nitration of acetylpentamethylbenzene (APMB), 1-acetyl-2,3,4,6-tetramethylbenzene (ATMB), and 1-benzoyl-2,3,4,6-tetramethylbenzene (BTMB) and the resulting product distribution were investigated.Friedel-Crafts acylation, bromination, and deuteration of APMB and Friedel-Crafts acylation of ATMB gave deacetylation-substitution products.On the other hand, bromination and deuteration of ATMB (or BTMB) and Friedel-Crafts acylation of BTMB gave 5-substituted products.In both cases, the positional reactivities were in accordance with the relative ?-complex stability.Conversely, except for Friedel-Crafts-type nitration, the positional reactivities in the nitration of these substrates were strikingly different from those of the above three reactions.Thus, side-chain functionalization at the 6-methyl group occurred in nitration with fuming nitric acid, depending on the solvents in use.The NMDO calculations and the reaction of APMB with single-electron transfer reagents such as tetranitromethane-hν or cerium(IV) ammonium nitrate suggest that the product distribution in nitration can be explained in terms of a single-electron transfer mechanism.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 2142-78-1