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6-Chloro-2-methyl-benzoxazole, a chemical compound with the molecular formula C8H6ClNO, is a benzoxazole derivative characterized by the presence of a chlorine atom and a methyl group attached to the benzene ring. 6-CHLORO-2-METHYL-BENZOXAZOLE is known for its wide range of chemical reactivity and is utilized in various organic synthesis processes. It is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes, and has been studied for its potential biological and pharmacological activities. Due to its potential hazards, it is important to handle this chemical compound with caution and in accordance with proper safety protocols.

63816-18-2

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63816-18-2 Usage

Uses

Used in Pharmaceutical Industry:
6-Chloro-2-methyl-benzoxazole is used as an intermediate in the synthesis of various pharmaceuticals for its wide range of chemical reactivity and potential biological and pharmacological activities.
Used in Agrochemical Industry:
This benzoxazole derivative is utilized as an intermediate in the synthesis of agrochemicals, contributing to the development of effective pesticides and other agricultural products.
Used in Dye Industry:
6-Chloro-2-methyl-benzoxazole is employed in the synthesis of dyes, where its chemical properties are leveraged to create a variety of colorants for different applications.
Used in Organic Synthesis Processes:
Due to its versatile chemical reactivity, 6-chloro-2-methyl-benzoxazole is used in various organic synthesis processes to produce a range of chemical compounds for diverse applications across industries.

Check Digit Verification of cas no

The CAS Registry Mumber 63816-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,1 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 63816-18:
(7*6)+(6*3)+(5*8)+(4*1)+(3*6)+(2*1)+(1*8)=132
132 % 10 = 2
So 63816-18-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H6ClNO/c1-5-10-7-3-2-6(9)4-8(7)11-5/h2-4H,1H3

63816-18-2SDS

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 6-Chloro-2-methylbenzo[d]oxazole

1.2 Other means of identification

Product number -
Other names 6-chloro-2-methyl-1,3-benzoxazole

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:63816-18-2 SDS

63816-18-2Downstream Products

63816-18-2Relevant academic research and scientific papers

Synthesis of benzoxazoles from 2-aminophenols and β-diketones using a combined catalyst of br?nsted acid and copper iodide

Mayo, Muhammad Shareef,Yu, Xiaoqiang,Zhou, Xiaoyu,Feng, Xiujuan,Yamamoto, Yoshinori,Bao, Ming

, p. 6310 - 6314 (2014/07/21)

Cyclization reactions of 2-aminophenols with β-diketones catalyzed by a combination of Br?nsted acid and CuI are presented. Various 2-substituted benzoxazoles were obtained through these reactions. Different substituents such as methyl, chloro, bromo, nitro, and methoxy on 2-aminophenol are tolerated under the optimized reaction conditions.

Reexamination of the Thermolytic Rearrangement of 4-Halophenyl Azides to 2-Aminophenols and other Products

Gershon, H.,Clarke, D. D.,Gershon, M.

, p. 367 - 380 (2007/10/02)

The halogenation of derivatives of 2-aminophenol with N-chloro- and N-bromosuccinimides at ambient temperatures in acetic acid was studied.With the necessary compounds available, a reexamination of the thermolytic rearrangement of 2-halophenyl azides to 2-aminophenols and other products was undertaken.It is certain that the rearrangement of 4-halophenyl azides to 2-aminophenols occurs but the products identified in this study differ significantly from those reported previously by Suschitzky et al. (1963, 1966). Keywords: Acetylated-2-amino-5-halophenols; 2-Acetamido-5-haloanisoles; 6-Halo-2-methylbenzoxazoles; 6-Halobenzoxazolones; 6-Halotriacetylaminophenols; 1H-NMR spectra; Fungicidal activity.

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