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26530-24-5

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26530-24-5 Usage

Chemical Properties

Light Yellow Oil

Check Digit Verification of cas no

The CAS Registry Mumber 26530-24-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,3 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 26530-24:
(7*2)+(6*6)+(5*5)+(4*3)+(3*0)+(2*2)+(1*4)=95
95 % 10 = 5
So 26530-24-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H18ClNOS/c1-2-3-4-5-6-7-8-13-11(14)9-10(12)15-13/h9H,2-8H2,1H3

26530-24-5SDS

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 5-chloro-2-octyl-1,2-thiazol-3-one

1.2 Other means of identification

Product number -
Other names 5-chloro-2-n-octyl-3-isothiazolone

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:26530-24-5 SDS

26530-24-5Downstream Products

26530-24-5Relevant articles and documents

5-chloro-alkyl isothiazolinone preparation method

-

Paragraph 0031-0040, (2020/02/10)

The invention relates to a 5-chloro-alkyl isothiazolinone preparation method, which comprises: (1) adding a transition metal halide and crown ether as catalysts and a substrate dialkyl-3,3-dithiodipropionamide into an organic solvent, introducing chlorine, and carrying out a ring-closure reaction at a reaction temperature of less than 0 DEG C for 1-3 h; (2) introducing a mixed gas of chlorine andan inert gas into the reaction, and controlling the temperature at -10 to 10 DEG C and the reaction time at 1-3 h; and (3) when the proportion of the substrate in the reaction system is less than or equal to 10%, stopping the reaction. According to the invention, the yield of the 5-chloro-alkyl isothiazolinone prepared by the method is remarkably higher than the yield of the polychloroalkyl isothiazolinone reported at present, and the fungus inhibition rate of the 5-chloro-alkyl isothiazolinone is equivalent to the fungus inhibition rate of the mainstream bactericide component 4,5-dichloro-octyl isothiazolinone on the market at present; and the preparation method is widely applied to bactericide and preservative formulas in multiple fields.

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