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6-Benzothiazolemethanol,2-methyl-(6CI), also known as (2-Methyl-1,3-benzothiazol-6-yl)methanol, is an organic compound with the molecular formula C8H9NOS. It features a benzothiazole core structure with a methyl group at the 2nd position and a hydroxymethyl group at the 6th position. 6-Benzothiazolemethanol,2-methyl-(6CI) is known for its potential applications in the synthesis of various chemical compounds, particularly thiazole derivatives.

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  • 103440-65-9 Structure
  • Basic information

    1. Product Name: 6-Benzothiazolemethanol,2-methyl-(6CI)
    2. Synonyms: 6-Benzothiazolemethanol,2-methyl-(6CI);(2-methylbenzo[d]thiazol-6-yl)methanol
    3. CAS NO:103440-65-9
    4. Molecular Formula: C9H9NOS
    5. Molecular Weight: 179.23886
    6. EINECS: N/A
    7. Product Categories: BENZOTHIAZOLE
    8. Mol File: 103440-65-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: 6-Benzothiazolemethanol,2-methyl-(6CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-Benzothiazolemethanol,2-methyl-(6CI)(103440-65-9)
    11. EPA Substance Registry System: 6-Benzothiazolemethanol,2-methyl-(6CI)(103440-65-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 103440-65-9(Hazardous Substances Data)

103440-65-9 Usage

Uses

Used in Pharmaceutical Industry:
6-Benzothiazolemethanol,2-methyl-(6CI) is used as a key intermediate in the synthesis of thiazole derivatives, which are important for the development of various pharmaceutical compounds. These derivatives have been found to possess a range of biological activities, including antimicrobial, antifungal, and anticancer properties.
Used in Chemical Synthesis:
In the field of chemical synthesis, 6-Benzothiazolemethanol,2-methyl-(6CI) serves as a versatile building block for the creation of a wide array of thiazole-based compounds. These compounds can be further modified and functionalized to explore their potential applications in various industries, such as agriculture, materials science, and pharmaceuticals.
Used in Research and Development:
6-Benzothiazolemethanol,2-methyl-(6CI) is also utilized in research and development laboratories for the study of its chemical properties and reactivity. This helps scientists and researchers to better understand the structure-activity relationships of thiazole derivatives and to design new compounds with improved properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 103440-65-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,4,4 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 103440-65:
(8*1)+(7*0)+(6*3)+(5*4)+(4*4)+(3*0)+(2*6)+(1*5)=79
79 % 10 = 9
So 103440-65-9 is a valid CAS Registry Number.

103440-65-9SDS

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-Methyl-1,3-benzothiazol-6-yl)methanol

1.2 Other means of identification

Product number -
Other names 2-Methyl-6-hydroxymethyl-benzothiazol

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:103440-65-9 SDS

103440-65-9Relevant articles and documents

NOVEL JNK INHIBITORS

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Page/Page column 103, (2008/12/07)

Disclosed are substituted imidazo[1,2-a]pyridines, imidazo[1,2-a]pyrazines, imidazo[1,2-c]pyrimidines and imidazo[1,2-d]triazines compounds of the formula: (1.0) Also disclosed are methods for treating JNK1 and ERK mediated diseases using the compounds of formula 1.0.

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