| Company Name: |
BePharm Ltd
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| Tel: |
400-685-9117 |
| Email: |
market@bepharm.com |
| Products Intro: |
Product Name:4-Chloro-3-methylbenzo[d]thiazol-2(3H)-one
CAS:63755-05-5
Purity:98% Package:5542RMB/1g
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| Company Name: |
CHEMICAL LAND21
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| Tel: |
82- 2 -783 - 8063 |
| Email: |
sales21@chemicalland21.com |
| Products Intro: |
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| | Chlobenthiazone Basic information |
| Product Name: | Chlobenthiazone | | Synonyms: | Chlobenthiazone;4-Chloro-3-methyl-2,3-dihydrobenzothiazol-2-one;4-Chloro-3-methylbenzothiazol-2(3H)-one;4-Chloro-3-Methylbenzo[d]thiazol-2(3H)-one;2(3H)-Benzothiazolone, 4-chloro-3-methyl-;Phenylephrine Impurity 101 | | CAS: | 63755-05-5 | | MF: | C8H6ClNOS | | MW: | 199.66 | | EINECS: | | | Product Categories: | | | Mol File: | 63755-05-5.mol |  |
| | Chlobenthiazone Chemical Properties |
| storage temp. | 2-8°C | | Henry's Law Constant | 1.3×100 mol/(m3Pa) at 25℃, MacBean (2012) |
| | Chlobenthiazone Usage And Synthesis |
| Description | Chlobenthiazone is a rice fungicide for controlling blast. It has a moderate aqueous solubility and is highly volatile. Little is known about its environmental fate or ecotoxicological properties. It is moderately toxic to mammals if ingested. | | Production Methods | The production of chlobenthiazone involves the chemical synthesis of 4-chloro-3-methylbenzothiazol-2(3H)-one, typically starting from precursors like 4-chloro-2-methoxybenzothiazole. The process includes chlorination and methylation steps, often carried out in organic solvents such as chloroform with bases like triethylamine or DBU to facilitate the reaction, achieving high yields of up to 98%. | | Mechanism of action | Systemic, inhibits infection sites, strong inhibitor of aflatoxin synthesis by A. flavus | | Pesticide Type | Fungicide |
| | Chlobenthiazone Preparation Products And Raw materials |
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