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Isothiazole-5-methanol, also known as 5-Isothiazolemethanol, is an organic compound with the molecular formula C4H5NO2S. It is a key intermediate in the synthesis of various pharmaceuticals and exhibits unique chemical properties that make it valuable in the development of new drugs and materials.

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  • 1710-66-3 Structure
  • Basic information

    1. Product Name: Isothiazole-5-methanol
    2. Synonyms: 5-Isothiazolemethanol;Isothiazole-5-methanol;(isothiazol-5-yl)methanol;5-(Hydroxymethyl)isothiazole
    3. CAS NO:1710-66-3
    4. Molecular Formula: C4H5NOS
    5. Molecular Weight: 115.15
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1710-66-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 135.8°C at 760 mmHg
    3. Flash Point: 35.9°C
    4. Appearance: /
    5. Density: 1.339g/cm3
    6. Vapor Pressure: 5.66mmHg at 25°C
    7. Refractive Index: 1.594
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 13.61±0.10(Predicted)
    11. CAS DataBase Reference: Isothiazole-5-methanol(CAS DataBase Reference)
    12. NIST Chemistry Reference: Isothiazole-5-methanol(1710-66-3)
    13. EPA Substance Registry System: Isothiazole-5-methanol(1710-66-3)
  • 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: 1710-66-3(Hazardous Substances Data)

1710-66-3 Usage

Uses

Used in Pharmaceutical Industry:
Isothiazole-5-methanol is used as a key intermediate in the synthesis of 1β-methylcarbapenems, a class of antibiotics with isothiazoloethenyl side chains. These antibiotics exhibit potent antibacterial activities, making them effective against a wide range of bacterial infections. The incorporation of Isothiazole-5-methanol into the structure of these antibiotics enhances their efficacy and broadens their spectrum of activity, providing a valuable tool in the fight against antibiotic-resistant bacteria.

Check Digit Verification of cas no

The CAS Registry Mumber 1710-66-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,1 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1710-66:
(6*1)+(5*7)+(4*1)+(3*0)+(2*6)+(1*6)=63
63 % 10 = 3
So 1710-66-3 is a valid CAS Registry Number.
InChI:InChI=1/C4H5NOS/c6-3-4-1-2-5-7-4/h1-2,6H,3H2

1710-66-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-thiazol-5-ylmethanol

1.2 Other means of identification

Product number -
Other names Isothiazol-5-ylmethanol

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:1710-66-3 SDS

1710-66-3Relevant articles and documents

Synthesis and biological evaluation of novel 1β-methylcarbapenems with isothiazoloethenyl side chains

Kang, Yong Koo,Lee, Kyung Seok,Yoo, Kyung Ho,Shin, Kye Jung,Kim, Dong Chan,Lee, Chang-Seok,Kong, Jae Yang,Kim, Dong Jin

, p. 463 - 466 (2007/10/03)

The synthesis of novel 1β-methylcarbapenems 1a,b bearing isothiazoloethenyl moieties at C-5 position of pyrrolidine ring and their biological evaluation are described. Both compounds showed potent and well-balanced antibacterial activity as well as high stability to DHP-I. Especially, 5-isothiazole derivative 1a exhibited excellent DHP-I stability and advanced pharmacokinetics profiles, compared to 5-isoxazole derivative 2, imipenem, and meropenem.

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