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2-Chloro-6-methylanisole, a chlorinated derivative of anisole with the molecular formula C8H9ClO, is a methoxy-substituted benzene derivative. It is a clear liquid with a sweet, floral odor and is considered to have low toxicity. Due to its unique chemical properties, it is used in various applications across different industries.

3438-15-1

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3438-15-1 Usage

Uses

Used in Fragrance and Flavor Industry:
2-Chloro-6-methylanisole is used as a fragrance and flavoring agent for its sweet, floral scent. It is incorporated into the production of perfumes, cosmetics, and food products to enhance their aroma and taste.
Used in Pharmaceutical Industry:
As an intermediate in the synthesis of pharmaceuticals, 2-CHLORO-6-METHYLANISOLE plays a crucial role in the development of various medications. Its unique chemical structure allows it to be a key component in the creation of new and innovative drugs.
Used in Agrochemical Industry:
2-Chloro-6-methylanisole is also utilized as an intermediate in the synthesis of agrochemicals. Its application in this industry contributes to the development of effective pesticides and other agricultural products.
It is important to handle 2-Chloro-6-methylanisole with caution and follow proper safety procedures in its handling and use to ensure the safety of both individuals and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 3438-15-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,3 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3438-15:
(6*3)+(5*4)+(4*3)+(3*8)+(2*1)+(1*5)=81
81 % 10 = 1
So 3438-15-1 is a valid CAS Registry Number.

3438-15-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-2-methoxy-3-methylbenzene

1.2 Other means of identification

Product number -
Other names 2-Chloro-6-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:3438-15-1 SDS

3438-15-1Relevant academic research and scientific papers

α,3-Didehydro-5-methyl-6-hydroxytoluene: Matrix isolation of a diradical related to the neocarzinostatin chromophore

Sander, Wolfram,Wandel, Holger,Bucher, G?tz,Gr?fenstein, Jürgen,Kraka, Elfi,Cremer, Dieter

, p. 8480 - 8485 (1998)

UV photolysis of 2,6-dimethylcyclohexa-2,5-dien-1-on-4-ylidene (4), matrix isolated in argon at 10 K, results in the formation of a labile species which is characterized as α,3-didehydro-5-methyl-6-hydroxybenzene (5) by comparison of the experimental IR s

Diphenyl ether derivative, pharmaceutical salts thereof and medicinal use

-

Paragraph 0271; 0272; 0273; 0274; 0275; 0276, (2019/02/19)

The invention relates to the field of pharmaceutical chemistry and discloses a compound (I) acting in the aspect of treating diseases related to PD-1/PD-L1 signal channels such as cancer, infectious diseases and autoimmune diseases, pharmaceutical salts a

ARYL FLUOROETHYL UREAS ACTING AS ALPHA 2 ADRENERGIC AGENTS

-

Page/Page column 25-26, (2008/12/07)

The invention provides well-defined aryl fluoroethyl ureas that are useful as selective alpha2 adrenergic agonists. As such, the compounds described herein are useful in treating a wide variety of disorders associated with modulation of alpha2 adrenergic receptors.

Two efficient methods for the preparation of 2-chloro-6-methylbenzoic acid

Daniewski, Andrzej R.,Liu, Wen,Puentener, Kurt,Scalone, Michelangelo

, p. 220 - 224 (2013/09/06)

Two efficient methods for the preparation of 2-chloro-6-methylbenzoic acid were developed: one based on nucleophilic aromatic substitution and the other based on carbonylation. In the first approach, 2-chloro-6-fluorobenzaldehyde was converted to its n-butylimine, then treated with 2 equiv of methylmagnesium chloride in THF to give, after hydrolysis, 2-chloro-6-methylbenzaldehyde. Subsequent oxidation of this compound gave the title compound in 85% overall yield. In the second approach, 3-chloro-2-iodotoluene was efficiently carbonylated in methanol to give methyl 2-chloro-6-methylbenzoate, which after hydrolysis afforded the title compound in 94% yield (84% yield after recrystallization). The carbomethoxylation proceeded smoothly even at a high substrate-to-Pd ratio of 10 000. Both methods do not require isolation of intermediates and are suitable for the preparation of kilogram quantities of 2-chloro-6-methylbenzoic acid.

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