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2-(4-Methoxyphenyl)isothiazolidine 1,1-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73825-54-4

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73825-54-4 Usage

Type of compound

Synthetic organic compound

Properties

Antimicrobial

Uses

Preservative in personal care products (shampoos, conditioners, liquid soaps), household and industrial cleaning products

Functioning

Inhibits the growth of bacteria and fungi, prolonging the shelf life of products

Health concerns

Associated with allergic reactions and skin irritation in some individuals

Regulations

Restricted or banned in some countries due to health concerns

Check Digit Verification of cas no

The CAS Registry Mumber 73825-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,8,2 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 73825-54:
(7*7)+(6*3)+(5*8)+(4*2)+(3*5)+(2*5)+(1*4)=144
144 % 10 = 4
So 73825-54-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H13NO3S/c1-14-10-5-3-9(4-6-10)11-7-2-8-15(11,12)13/h3-6H,2,7-8H2,1H3

73825-54-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methoxyphenyl)-1,2-thiazolidine 1,1-dioxide

1.2 Other means of identification

Product number -
Other names 2-(p-Methoxyphenyl)isothiazolidine-1,1-dioxide

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:73825-54-4 SDS

73825-54-4Downstream Products

73825-54-4Relevant academic research and scientific papers

Cross coupling of 3-bromopyridine and sulfonamides (R1NHSO2R2·R1 = H, Me, alkyl; R2 = alkyl and aryl) catalyzed by CuI/1,3-di(pyridin-2-yl)propane-1,3-dione

Han, Xiaojun

experimental part, p. 360 - 362 (2010/03/24)

N-(3-Pyridinyl)-substituted secondary and tertiary sulfonamides have been synthesized in good to excellent yields by the reaction of 3-bromopyridine with primary and secondary alkyl and aryl sulfonamides (MeSO2NH2, MeSO2NHMe, TolSO2NH2, TolSO2NHMe, 1,3-propanesultam, and 1,4-butanesultam), catalyzed by CuI (20 mol %) and 1,3-di(pyridin-2-yl)propane-1,3-dione (20 mol %) with K2CO3 (200 mol %) in DMF (0.17 M for ArBr) at 110-120 °C over 36-40 h. 2-Bromopyridine, 4-bromopyridine, and a wide variety of substituted phenyl bromides can also be successfully coupled with sulfonamides under these reaction conditions.

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