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3-Ethyl-2,3-dihydrobenzothiazol-2-on, also known as 3-ethyl-2,3-dihydrobenzothiazole-2-thione, is an organic compound with the chemical formula C9H11NS. It is a colorless to pale yellow crystalline solid that is soluble in organic solvents. 3-Ethyl-2,3-dihydrobenzothiazol-2-on is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and dyes. It is also known for its potential applications in the development of new materials with unique properties, such as conductive polymers and sensors. The compound is synthesized through various chemical reactions, including the condensation of ethylamine with 2-mercaptobenzothiazole. Due to its reactivity and potential applications, 3-ethyl-2,3-dihydrobenzothiazol-2-on is an important compound in the field of organic chemistry and material science.

6468-14-0

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6468-14-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6468-14-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,6 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6468-14:
(6*6)+(5*4)+(4*6)+(3*8)+(2*1)+(1*4)=110
110 % 10 = 0
So 6468-14-0 is a valid CAS Registry Number.

6468-14-0SDS

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 3-ethyl-1,3-benzothiazol-2-one

1.2 Other means of identification

Product number -
Other names 3-ethylbenzothiazol-2-one

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:6468-14-0 SDS

6468-14-0Relevant academic research and scientific papers

151. Azidinium-Salze. 24. Mitteilung. Thermolyse heterocyclischer Azidinium-tetrafluoroborate

Huys-Francotte, Martine,Balli, Heinz

, p. 1679 - 1684 (2007/10/02)

The thermolysis of some azidinium salts was investigated.It led to a large variety of products which were isolated or identified by GC/MS.Reaction mechanisms are discussed to explain the product formation.

REACTIONS OF POLYMETHINE DYES. I. SYNTHESIS OF THE PSEUDOBASES OF POLYMETHINE DYES AND THEIR TRANSFORMATIONS

Vompe, A. F.,Ivanova, L. V.,Meskhi, L. M.,Monich, N. V.,Raikhina, R. D.

, p. 529 - 537 (2007/10/02)

Nonsalt-like benzene-soluble pseudobases are formed in the reaction of polymethine dyes with sodium alcoholates.The presence of ionized and un-ionized forms of the pseudobases was established by electronic absorption spectra in aprotic solvents.Solutions of these compounds in alcohols only contain the ionized forms; the unionized form predominates in benzene solutions.The action of various acids on the pseudobases leads to the production of polymethine dyes with the respective anions.

Dication Ethers and Related Compounds, 1. On Dication Chalkogenides and Dichalkogenides

Maas, Gerhard,Singer, Berndt

, p. 3659 - 3674 (2007/10/02)

Reaction of N,N-, N,S-, S,S-, and O,O-substituted thiones 4a-f or selones 6a-c with trifluoromethanesulfonic anhydride leads to dication disulfides 5a-f or diselenides 7a-c, resp.No dication sulfides or selenides are obtained whose formation would parallel the reactivity of the corresponding urea derivatives.This class of dications (14, 15) is, on the other hand, accessible by the reaction of dication ethers 13 with thiones 4 or selones 6. 1H and 13C NMR data of the dication dichalkogenides and chalkogenides are compared with each other.

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