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Merck
CN

561487

噻霉酮

97%

别名:

1,2-苯并异噻唑-3-酮, 1,2-苯并异噻唑酮, 2,3-二氢-1,2-苯并噻唑-3-酮, 3-羟基-1,2-苯并异噻唑, 苯并异噻唑啉-3-酮

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关于此项目

经验公式(希尔记法):
C7H5NOS
化学文摘社编号:
分子量:
151.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
220-120-9
MDL number:
Assay:
97%
Form:
solid
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Quality Level

assay

97%

form

solid

mp

154-158 °C (lit.)

SMILES string

Oc1nsc2ccccc12

InChI

1S/C7H5NOS/c9-7-5-3-1-2-4-6(5)10-8-7/h1-4H,(H,8,9)

InChI key

DMSMPAJRVJJAGA-UHFFFAOYSA-N

General description

1,2-苯并异噻唑3(2H)-酮可以通过使2-巯基苯甲酸与二苯基磷酰基叠氮化物反应来合成。

Application

1,2-苯并异噻唑-3(2H)-酮可作为前体合成生物活性更高的1,2-苯并异噻唑啉-3-酮(BIT)。

Disclaimer

本品不可用作全球生物杀灭剂法规监管的生物杀灭剂,包括但不限于:美国联邦杀虫剂、杀菌剂和灭鼠剂法(US EPA′s Federal Insecticide Fungicide and Rodenticide Act)、欧盟生物杀灭剂法规(European Biocidal Products Regulation)、加拿大虫害管理监管机构(Canada’s Pest Management Regulatory Agency)、土耳其生物杀灭剂法规(Turkey’s Biocidal Products Regulation)、韩国生物杀灭剂法(Korea’s Consumer Chemical Products and Biocide Safety Management Act (K-BPR))等。


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signalword

Danger

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1A

存储类别

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

法规信息

农药列管产品

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历史批次信息供参考:

分析证书(COA)

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Convenient Synthesis of 1, 2-Benzisothiazol-3 (2H)-ones by Cyclization Reaction
of Acyl Azide
Chiyoda T, et al.
Synlett, 2000(10), 1427-1428 (2000)
Mahalakshmi Vasan et al.
ChemMedChem, 5(12), 2079-2087 (2010-11-06)
A simple steady-state kinetic high-throughput assay was developed for the salicylate synthase MbtI from Mycobacterium tuberculosis, which catalyzes the first committed step of mycobactin biosynthesis. The mycobactins are small-molecule iron chelators produced by M. tuberculosis, and their biosynthesis has been identified
Dengfeng Dou et al.
Bioorganic & medicinal chemistry, 19(19), 5782-5787 (2011-09-10)
A series of broad-spectrum antifungal agents based on the 1,2-benzisothiazol-3(2H)-one scaffold is reported. Preliminary structure-activity relationship studies have established the importance of the presence of the heterocyclic ring, a methyl group, and a phenyl ring for optimal manifestation of antifungal



全球贸易项目编号

货号GTIN
561487-25G04061832583518
561487-5G04061832583525