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5-Benzothiazolol, also known as 5-Benzothiazole or 5-thia-1-azabicyclo[4.2.0]octa-1,3,5-triene, is a heterocyclic compound characterized by the fusion of a benzene ring to a thiazole ring. It possesses the molecular formula C7H5NS and a molecular weight of 135.19 g/mol. This pale yellow to brown solid has a melting point of 140-142°C, is sparingly soluble in water, and is soluble in organic solvents like ethanol and ether. Recognized for its low toxicity, 5-Benzothiazolol is utilized as a building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds, as well as a ligand in organometallic chemistry for the preparation of metal complexes.

7686-41-1

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7686-41-1 Usage

Uses

Used in Pharmaceutical Industry:
5-Benzothiazolol(7CI,8CI,9CI) is used as a building block for the synthesis of various pharmaceuticals due to its unique heterocyclic structure, which can be incorporated into drug molecules to enhance their therapeutic properties and effectiveness.
Used in Agrochemical Industry:
In the agrochemical sector, 5-Benzothiazolol(7CI,8CI,9CI) serves as a key component in the development of agrochemicals, contributing to the creation of compounds that can improve crop protection and yield.
Used in Organic Synthesis:
5-Benzothiazolol(7CI,8CI,9CI) is utilized as an intermediate in organic synthesis, allowing for the construction of a wide range of organic compounds with diverse applications in various industries.
Used in Organometallic Chemistry:
As a ligand in organometallic chemistry, 5-Benzothiazolol(7CI,8CI,9CI) is employed in the preparation of metal complexes, which have potential applications in catalysis, materials science, and other advanced chemical processes.
Proper handling and storage of 5-Benzothiazolol(7CI,8CI,9CI) are essential to ensure safety and minimize potential risks associated with its use in these applications.

Check Digit Verification of cas no

The CAS Registry Mumber 7686-41-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,8 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7686-41:
(6*7)+(5*6)+(4*8)+(3*6)+(2*4)+(1*1)=131
131 % 10 = 1
So 7686-41-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H5NOS/c9-5-1-2-7-6(3-5)8-4-10-7/h1-4,9H

7686-41-1SDS

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 1,3-benzothiazol-5-ol

1.2 Other means of identification

Product number -
Other names benzothiazol-5-ol

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:7686-41-1 SDS

7686-41-1Relevant academic research and scientific papers

Method for synthesizing benzothiazole by microwave radiation of benzothioamide compound in aqueous phase

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Paragraph 0013; 0066, (2019/02/13)

The invention discloses a method for synthesizing benzothiazole by microwave radiation of a benzothioamide compound in an aqueous phase. The method includes the steps: adding the benzothioamide compound into the aqueous phase under microwave conditions; performing cyclization under alkaline conditions to generate the benzothiazole. The method for preparing the benzothiazole is environmentally friendly, simple and convenient in operation, safe, cheap and efficient. Compared with the prior art, the method is applicable to a lot of functional groups, high in yield, few in by-products, simple in operation, safe, low in cost and environmentally friendly.

FUNCTIONALLY SELECTIVE LIGANDS OF DOPAMINE D2 RECEPTORS

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, (2012/01/15)

The present invention relates to novel functionally selective ligands of dopamine D2 receptors, including agonists, antagonists, and inverse agonists. The invention further relates to the use of these compounds for treating central nervous system disorders related to D2 receptors.

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