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6265-94-7

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6265-94-7 Usage

Description

Benzothiazole, 2-(phenylmethyl)(9CI) is a chemical compound with the molecular formula C15H11NS. It is a benzothiazole derivative that is commonly used in the production of various organic compounds and materials. This chemical is known for its wide range of applications, including as a building block for pharmaceuticals, agricultural chemicals, and rubber industries. It is also used in research and development, as well as in the manufacturing of dyes and as an intermediate in organic synthesis. Benzothiazole, 2-(phenylmethyl)(9CI) is considered to be a versatile and valuable compound in the chemical industry due to its unique properties and potential applications.

Uses

Used in Pharmaceutical Industry:
Benzothiazole, 2-(phenylmethyl)(9CI) is used as a building block for the development of various pharmaceuticals. Its unique chemical structure allows it to be incorporated into drug molecules, potentially enhancing their therapeutic properties and effectiveness.
Used in Agricultural Chemicals Industry:
In the agricultural chemicals industry, Benzothiazole, 2-(phenylmethyl)(9CI) is utilized as a component in the synthesis of various agrochemicals. Its versatility enables it to be a key part of the development of new and improved products for crop protection and other agricultural applications.
Used in Rubber Industry:
Benzothiazole, 2-(phenylmethyl)(9CI) is employed in the rubber industry as a component in the production of various rubber materials. Its properties can contribute to the improvement of rubber's performance, durability, and other characteristics.
Used in Research and Development:
Benzothiazole, 2-(phenylmethyl)(9CI) is also used in research and development for the exploration of new chemical reactions and the synthesis of novel organic compounds. Its unique structure and properties make it a valuable tool for scientists and researchers in the chemical industry.
Used in Dye Manufacturing:
Benzothiazole, 2-(phenylmethyl)(9CI) is utilized in the manufacturing of dyes, where its chemical properties can contribute to the development of new and improved dyes with enhanced color and performance characteristics.
Used as an Intermediate in Organic Synthesis:
Finally, Benzothiazole, 2-(phenylmethyl)(9CI) serves as an intermediate in organic synthesis, where it can be used to produce a wide range of organic compounds for various applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 6265-94-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,6 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6265-94:
(6*6)+(5*2)+(4*6)+(3*5)+(2*9)+(1*4)=107
107 % 10 = 7
So 6265-94-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H11NS/c1-2-6-11(7-3-1)10-14-15-12-8-4-5-9-13(12)16-14/h1-9H,10H2

6265-94-7SDS

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 2-benzyl-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names 2-Benzylbenzothiazol

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:6265-94-7 SDS

6265-94-7Relevant articles and documents

Piezochromic luminescence behaviors of two new benzothiazole-enamido boron difluoride complexes: Intra- and inter-molecular effects induced by hydrostatic compression

Wang, Xiaoqing,Liu, Qingsong,Yan, Hui,Liu, Zhipeng,Yao, Mingguang,Zhang, Qingfu,Gong, Shuwen,He, Weijiang

, p. 7497 - 7500 (2015)

Two new propeller-shaped benzothiazole-enamide boron difluoride complexes exhibiting piezochromic luminescence upon mechanical grinding or hydrostatic compression were prepared. The two analogues displayed the red shift in luminescence under high pressure, while compound 2 with ICT effects showed a more sensitive piezochromic response at low pressure (1.5 GPa). The different piezochromic luminescence behaviors of these compounds were investigated. This journal is

Elemental Sulfur-Promoted Benzoxazole/Benzothiazole Formation Using a C=C Double Bond as a One-Carbon Donator

Chen, Xuecheng,Han, Shiqing,Hu, Liang,Liu, Yafei,Luo, Yue,Pan, Bin,Peng, Yalan,Zhang, Jun,Zhang, Yurong

, p. 14485 - 14492 (2021/11/12)

An efficient method to assemble diverse benzoxazoles/benzothiazoles in good yields was developed via oxidative cyclization with 2-aminothiophenols or 2-iodoanilines as raw materials. In this protocol, elemental sulfur was used as the effective oxidant and C atoms on the C=C double bond were introduced as a one-carbon donator.

C2-arylacylation of 2H-benzothiazoles with methyl arenes via Selectfluor oxidation

Chen, Bo,Kong, Yao-Lei,Liu, Jin-Chuan,Lu, Qi,Sun, Xiao-Tong,Weng, Jian-Quan

supporting information, (2021/06/03)

An efficient Selectfluor-oxidative protocol was developed for the direct C2-arylacylation of 2H-benzothiazoles via the radical reaction of 2H-benzothiazoles with methyl arenes. Selectfluor can effectively promote the oxidative cross-coupling without an ex

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