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1-CHLORO-3-METHOXY-5-METHYLBENZENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82477-66-5

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82477-66-5 Usage

Chemical Structure

1-chloro-3-methoxy-5-methylbenzene

Explanation

This describes the arrangement of atoms and functional groups in the molecule. The chlorine atom is at the 1 position, the methoxy group is at the 3 position, and the methyl group is at the 5 position on the benzene ring.

Explanation

The compound is derived from benzene, a basic aromatic hydrocarbon with a six-carbon ring and three double bonds.

Explanation

These are the specific functional groups present in the molecule, which contribute to its chemical properties and reactivity.

Explanation

The compound is used in the production of various products, including those in the pharmaceutical and agrochemical industries, as well as other industrial applications.

Explanation

The compound may have harmful effects on human health if not handled and disposed of properly.

Explanation

The compound may have negative effects on the environment if not managed correctly during its production, use, and disposal.

Explanation

Due to its potential toxic and environmental effects, it is essential to handle and dispose of the compound with caution to prevent harm to human health and the environment.

Derivative of Benzene

Yes

Functional Groups

Chlorine atom, methoxy group, and methyl group

Applications

Pharmaceutical, agrochemical, and industrial products

Toxicity

Potential toxic effects

Environmental Impact

Potential environmental effects

Handling and Disposal

Careful management required

Check Digit Verification of cas no

The CAS Registry Mumber 82477-66-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,4,7 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 82477-66:
(7*8)+(6*2)+(5*4)+(4*7)+(3*7)+(2*6)+(1*6)=155
155 % 10 = 5
So 82477-66-5 is a valid CAS Registry Number.

82477-66-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-CHLORO-3-METHOXY-5-METHYLBENZENE

1.2 Other means of identification

Product number -
Other names 3-CHLORO-5-METHYLANISOLE

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:82477-66-5 SDS

82477-66-5Relevant academic research and scientific papers

Synthesis method of 1-chloro-3-methoxy-5-methyl benzene

-

Paragraph 0025-0045, (2021/10/20)

The invention belongs to the technical field of synthesis of medical compounds, and particularly discloses a synthesis method of 1-chloro-3-methoxy-5-methyl benzene. According to the synthesis method provided by the invention, 1-chlorine-3-halogenated toluene is adopted as a raw material, and the 1-chlorine-3-methoxy-5-methyl benzene is prepared through heating reaction of the 1-chlorine-3-halogenated toluene and sodium methoxide. The method has the advantages of cheap and easily available raw materials, convenience in production and easiness in purification, and can be developed into an industrial production method.

A New Synthesis of Defucogilvocarcin M

Hart, David J.,Merriman, Gregory H.

, p. 5093 - 5096 (2007/10/02)

A convergent synthesis of the title compound is described.The synthesis revolves around a MAD-mediated coupling of oxazoline 11 and naphthoquinone ketal 16 and requires eight steps via the longest linear sequence.

Reaction of Some 1,4-Benzoquinone Mono-oximes with Methanolic Hydrogen Chloride

Sargent, Melvyn V.

, p. 1095 - 1098 (2007/10/02)

When 2-methyl-1,4-benzoquinone 4-oxime (1) reacted with methanolic hydrogen chloride at 25-30 deg C the product was 2-chloro-4,6-dimethoxy-3-methylaniline (2).Similarly 1,4-benzoquinone 4-oxime (7) gave 2-chloro-4,6-dimethoxyaniline (8), 3-methyl-1,4-benzoquinone 4-oxime (11) gave 2-chloro-4-methoxy-6-methoxymethylaniline (12) and 2-chloro-4-methoxy-6-methylaniline (13), and 2-methoxy-1,4-benzoquinone 4-oxime (19) gave 2-chloro-4,5-dimethoxyaniline (20).

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