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3905-43-9

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3905-43-9 Usage

Appearance

White to off-white solid

Solubility

Sparingly soluble in water

Formation

Result of the reaction between 1,2-benzenediol (catechol) and dibenzenesulfonate

Industrial Applications

a. Stabilizer in polyvinyl chloride (PVC) plastics
b. Intermediate in the synthesis of other chemicals

Additional Uses

a. Corrosion inhibitor in water treatment processes
b. Researched for potential pharmacological and biological properties
c. Investigated as a potential anti-cancer agent

Versatility

Wide range of uses across different industries

Check Digit Verification of cas no

The CAS Registry Mumber 3905-43-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,0 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3905-43:
(6*3)+(5*9)+(4*0)+(3*5)+(2*4)+(1*3)=89
89 % 10 = 9
So 3905-43-9 is a valid CAS Registry Number.

3905-43-9SDS

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 benzene-1,2-diol,benzenesulfonic acid

1.2 Other means of identification

Product number -
Other names 1,2-bis<(benzenesulfonyl)oxy>benzene

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:3905-43-9 SDS

3905-43-9Downstream Products

3905-43-9Relevant articles and documents

1-Phenylsulfonylbenzotriazole: A novel and convenient reagent for the preparation of benzenesulfonamides and aryl benzenesulfonates

Katritzky,Zhang,Wu

, p. 205 - 216 (2007/10/02)

Readily available 1-phenylsulfonylbenzotriazole smoothly converts various aliphatic and aromatic amines and phenols into the corresponding benzenesulfonamides and benzenesulfonates in good yields.

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