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

26542-16-5

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26542-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26542-16-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,4 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 26542-16:
(7*2)+(6*6)+(5*5)+(4*4)+(3*2)+(2*1)+(1*6)=105
105 % 10 = 5
So 26542-16-5 is a valid CAS Registry Number.

26542-16-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Tert-Butyl)Isothiazol-3(2H)-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:26542-16-5 SDS

26542-16-5Relevant academic research and scientific papers

The synthesis of N-substituted isothiazol-3(2H)-ones from N-substituted 3-benzoylpropionamides

Hamilakis, Stylianos,Kontonassios, Demetrios,Tsolomitis, Athanase

, p. 149 - 155 (2007/10/03)

N-Substituted isothiazol-3(2H)-ones can be easily prepared from N-substituted 3-benzoylpropionamides in two experimentally simple steps, in satisfactory overall yields. Reaction of the amides with excess thionyl chloride results in the formation of N-subs

Facile synthesis of N-substituted isothiazol-3(2H)-ones using a hypervalent iodine(III) reagent

Kang, Iou-Jiun,Wang, Huey-Min,Huang, Hsin-Yu,Chen, Ling-Ching

, p. 1185 - 1188 (2007/10/03)

Treatment of N-substituted (Z)-3-(benzylsulfanyl)propenamides (4) with phenyliodine(III) bis(trifluoroacetate) containing trifluoroacetic acid resulted in an interrupted Pummerer-type reaction to give N-substituted isothiazol-3(2H)-ones (5) rather than th

A General Synthesis of N-Substituted Isothiazol-3(2H)-ones

Beeley, Nigel R. A.,Harwood, Laurence M.,Hedger, Paul C.

, p. 2245 - 2252 (2007/10/02)

A general route to the synthesis of N-substituted isothiazol-3(2H)-ones (4a-i) is described which proceeds via trichloroacetic acid-mediated ring closure of N-substituted (Z)-3-(benzylsulfinyl)propenamides (15a-i).

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