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2-Benzothiazolamine,6-chloro-4-methyl-(9CI) is a chloro-substituted derivative of 2-benzothiazolamine, an organic compound belonging to the benzothiazoles class. It has the molecular formula C9H7ClNS, a molecular weight of 203.68 g/mol, and features a chlorine atom and a methyl group attached to the benzothiazole ring. This yellowish crystalline solid has a melting point of approximately 97-99°C, is sparingly soluble in water, and soluble in organic solvents. It is commonly used in the synthesis of pharmaceuticals and agrochemicals, with potential applications in other industries as well.

38338-21-5

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38338-21-5 Usage

Uses

Used in Pharmaceutical Industry:
2-Benzothiazolamine,6-chloro-4-methyl-(9CI) is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Benzothiazolamine,6-chloro-4-methyl-(9CI) serves as a building block for the creation of novel agrochemicals. Its incorporation into these products can enhance their effectiveness in pest control and crop protection.
Used in Other Industrial Applications:
Although not explicitly mentioned in the provided materials, 2-Benzothiazolamine,6-chloro-4-methyl-(9CI) may also have applications in other industries, such as in the development of dyes, pigments, or other specialty chemicals, due to its unique chemical properties and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 38338-21-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,3,3 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38338-21:
(7*3)+(6*8)+(5*3)+(4*3)+(3*8)+(2*2)+(1*1)=125
125 % 10 = 5
So 38338-21-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H7ClN2S/c1-4-2-5(9)3-6-7(4)11-8(10)12-6/h2-3H,1H3,(H2,10,11)

38338-21-5SDS

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 6-chloro-4-methyl-1,3-benzothiazol-2-amine

1.2 Other means of identification

Product number -
Other names 6-Chloro-4-methyl-benzothiazol-2-ylamine

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:38338-21-5 SDS

38338-21-5Relevant academic research and scientific papers

Synthesis and insecticidal evaluation of novel sulfide-containing amide derivatives as potential ryanodine receptor modulators

Zhang, Yan,Li, Yuxin,Li, Huan,Shang, Junfeng,Li, Zhengming,Wang, Baolei

supporting information, p. 501 - 507 (2021/06/15)

With the aim of discovering new bioactive pesticides for crop protection, a series of novel sulfide-containing amide derivatives A were efficiently synthesized via a strategy of modifying the “amide” structure of anthranilic diamide insecticides. The single-crystal structures of A2-3 and A4-5 were firstly reported. The bioassay results showed that most of the synthesized compounds display moderate to high insecticidal activities. Particularly, some sulfone-containing compounds, e.g., A2-3, A3-3 and A6-3, not only possessed favorable lethality rate (50%–100%) against P. xylostella at a concentration of 0.1 mg/L, but also held good activities towards a variety of agricultural pests such as M. separata, C. pipiens pallen, H. armigera and O. nubilalis; the larvicidal activities of A4-1 and A6-1 towards P. xylostella were close to that of chlorantraniliprole at 0.01 mg/L. The calcium imaging experiments revealed that the representative compounds A2-3 and A6-3 are potential ryanodine receptor (RyR) modulators. The structure–activity relationships were discussed in detail. These results provide useful information for further design and development of novel insecticides.

Pyrazolecarboxamide derivative containing substituted sulfoximine acyl aryl as well as preparation method and application thereof

-

Paragraph 0046; 0051-0054, (2020/06/16)

The invention relates to a pyrazolecarboxamide derivative containing substituted sulfoximine acyl aryl as well as a preparation method and application thereof. On the basis of a sulfur-containing substituted arylamine intermediate, a compound obtained through a series of reactions is shown as a general formula I in the specification. The compound shown in the general formula I has good insecticidal activity, is especially effective to oriental armyworms and plutella xylostella, can be used as an active component of an insecticidal composition, is used for preparing agricultural insecticides, and is used for preventing and treating agricultural insect pests.

Synthesis and biological evaluation of novel N-pyridylpyrazolecarboxamides containing benzothiazole

Mao, Ming-Zhen,Wang, Hai-Yang,Wang, Wei,Ning, Bin-Ke,Li, Yu-Xin,Xiong, Li-Xia,Li, Zheng-Ming

, p. 42 - 46 (2016/12/24)

A series of novel N-pyridylpyrazolecarboxamides containing benzothiazolewere designed and synthesized. The target compounds were identified by 1H NMR,13C-NMR, IR, high-resolution mass spectrum (HRMS) and elemental analysis. The bioactivities of the newcom

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