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1-(3-Methoxy-5-methylphenyl)ethanone is an organic compound that belongs to the ketone family. It is characterized by the presence of a ketone group, a phenyl group, and a methyl and methoxy group attached to the phenyl ring. With a molecular formula of C10H12O2, 1-(3-Methoxy-5-methylphenyl)ethanone is also referred to as 1-(3-methoxy-5-methylphenyl)ethan-1-one or 1-(5-Methyl-3-methoxyphenyl)ethanone. Its properties, including melting point, boiling point, and density, can be influenced by factors such as temperature and pressure. For detailed handling and usage instructions, it is essential to consult the Material Safety Data Sheet.

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  • 43113-94-6 Structure
  • Basic information

    1. Product Name: 1-(3-Methoxy-5-methylphenyl)ethanone
    2. Synonyms: 1-(3-Methoxy-5-methylphenyl)ethanone;1-(3-Methoxy-5-Methylphenyl)ethan-1-one
    3. CAS NO:43113-94-6
    4. Molecular Formula: C10H12O2
    5. Molecular Weight: 164.2
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 43113-94-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 256.9°C at 760 mmHg
    3. Flash Point: 107.6°C
    4. Appearance: /
    5. Density: 1.018g/cm3
    6. Vapor Pressure: 0.015mmHg at 25°C
    7. Refractive Index: 1.504
    8. Storage Temp.: Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-(3-Methoxy-5-methylphenyl)ethanone(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-(3-Methoxy-5-methylphenyl)ethanone(43113-94-6)
    12. EPA Substance Registry System: 1-(3-Methoxy-5-methylphenyl)ethanone(43113-94-6)
  • 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: 43113-94-6(Hazardous Substances Data)

43113-94-6 Usage

Uses

Used in Organic Synthesis:
1-(3-Methoxy-5-methylphenyl)ethanone is utilized as an intermediate in the synthesis of various organic compounds. Its unique structure allows it to be a valuable building block in the creation of a wide range of chemical products.
Used in Chemical Manufacturing:
In the chemical industry, 1-(3-Methoxy-5-methylphenyl)ethanone is employed as a key component in the production of other chemicals. Its versatility and reactivity make it an essential ingredient in the formulation of different chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 43113-94-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,1,1 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 43113-94:
(7*4)+(6*3)+(5*1)+(4*1)+(3*3)+(2*9)+(1*4)=86
86 % 10 = 6
So 43113-94-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O2/c1-7-4-9(8(2)11)6-10(5-7)12-3/h4-6H,1-3H3

43113-94-6SDS

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 1-(3-Methoxy-5-methylphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 1-(3-Methoxy-5-methyl-phenyl)-ethanone

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:43113-94-6 SDS

43113-94-6Downstream Products

43113-94-6Relevant articles and documents

ISOQUINOLINE COMPOUNDS, A PROCESS FOR THEIR PREPARATION, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

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Paragraph 0272; 0273; 0274; 0927; 0928, (2017/06/12)

A compound of formula (I): wherein the substituents are as defined in the description. Medicinal products containing the same which are useful in treating or preventing pathologies which are the result of activation of the RhoA/ROCK pathway and phosphorylation of the myosin light chain.

The first total synthesis of (±)-γ-herbertenol, a herbertene isolated from a non-herbertus source

Srikrishna,Ravikumar

, p. 65 - 74 (2007/12/31)

The structure of the aromatic sesquiterpene, (±)-γ- herbertenol, the first herbertane to be isolated from a non-herbertus source, was confirmed by a total synthesis, employing a Claisen rearrangement and ring-closing metathesis. Georg Thieme Verlag Stuttg

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