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3-(2-HYDROXYETHYL)-1,3-BENZOTHIAZOL-2(3H)-ONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 21344-50-3 Structure
  • Basic information

    1. Product Name: 3-(2-HYDROXYETHYL)-1,3-BENZOTHIAZOL-2(3H)-ONE
    2. Synonyms: 3-(2-HYDROXYETHYL)-1,3-BENZOTHIAZOL-2(3H)-ONE
    3. CAS NO:21344-50-3
    4. Molecular Formula: C9H9NO2S
    5. Molecular Weight: 195.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 21344-50-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 386.1 °C at 760 mmHg
    3. Flash Point: 187.3 °C
    4. Appearance: /
    5. Density: 1.388 g/cm3
    6. Vapor Pressure: 1.18E-06mmHg at 25°C
    7. Refractive Index: 1.66
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-(2-HYDROXYETHYL)-1,3-BENZOTHIAZOL-2(3H)-ONE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-(2-HYDROXYETHYL)-1,3-BENZOTHIAZOL-2(3H)-ONE(21344-50-3)
    12. EPA Substance Registry System: 3-(2-HYDROXYETHYL)-1,3-BENZOTHIAZOL-2(3H)-ONE(21344-50-3)
  • 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: 21344-50-3(Hazardous Substances Data)

21344-50-3 Usage

Synthesis Reference(s)

Journal of Heterocyclic Chemistry, 25, p. 1601, 1988 DOI: 10.1002/jhet.5570250601

Check Digit Verification of cas no

The CAS Registry Mumber 21344-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,4 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21344-50:
(7*2)+(6*1)+(5*3)+(4*4)+(3*4)+(2*5)+(1*0)=73
73 % 10 = 3
So 21344-50-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NO2S/c11-6-5-10-7-3-1-2-4-8(7)13-9(10)12/h1-4,11H,5-6H2

21344-50-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-hydroxyethyl)-1,3-benzothiazol-2-one

1.2 Other means of identification

Product number -
Other names -

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:21344-50-3 SDS

21344-50-3Relevant articles and documents

Metal-free C(sp2)-H functionalization of azoles: K2CO3/I2-mediated oxidation, imination, and amination

Das, Ranajit,Banerjee, Mainak,Rai, Rakesh Kumar,Karri, Ramesh,Roy, Gouriprasanna

supporting information, p. 4243 - 4260 (2018/06/22)

The direct C2-H oxidation and imination of a wide variety of azoles was achieved by using a commercially available simple K2CO3/I2 reagent combination. The iodinated azole adduct, produced via the in situ generation of N-heterocyclic carbene, is the key intermediate for C2-H oxidation, imination, and amination of azoles. Significantly, these reactions proceed under mild conditions with high to excellent yields, are scalable to large quantity and exhibit a broad substrate scope. Interestingly, this direct C2-H imination method allowed us to access various pharmacologically active N6-alkyl or N6-aryl substituted benzimidazoquinazolinone scaffolds through intramolecular C-H imination in a sequential one-pot reaction.

Carbamates, Thiolcarbamates, Dithiocarbamates and Thioncarbamates Derived From 2-Benzothiazolinone and Benzoxazolinone

D'Amico, John J.,Bollinger, Frederic G.

, p. 655 - 660 (2007/10/02)

The reaction of 3-(2-hydroxyethyl)-2-benzothiazoline with methyl, phenyl isocyanate, or dimethylcarbamoyl chloride afforded the carbamates 1-4.The carbanilate 5 was prepared by the reaction of 2-benzothiazolinone with 3-chloropropyl-N-methylcarbanilate un

Derivatives of 3-(2-Hydroxyethyl)-2-benzothiazolinone and Related Compounds

D'Amico, John J.,Bollinger, Frederic G.

, p. 1601 - 1605 (2007/10/02)

The reaction of the appropriate 2-benzothiazolinone with 2-chloroethanol or 3-chloropropanol under basic conditions afforded 3-(2-hydroxyethyl- or 3-hydroxypropyl)-2-benzothiazolinone and related compounds 1-7.The reaction of the alcohols 1, 4, 5, or 7 wi

N-Substituted oxobenzothiazolines and their use as plant growth regulators

-

, (2008/06/13)

This invention relates to novel N-substituted oxobenzothiazolines and to their use in a method of regulating leguminous plant growth as well as to plant growth regulant compositions.

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