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2,4-Dihydroxythiophenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

2553-70-0

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2553-70-0 Usage

Appearance

Colorless to white solid at room temperature

Solubility

Soluble in various organic solvents

Uses

Manufacturing of pharmaceuticals, dyes, and other organic compounds; intermediate in the synthesis of pesticides and other industrial chemicals

Odor

Distinct

Toxicity

Moderately toxic if ingested or inhaled in large quantities

Carcinogenicity

Not found to be carcinogenic

Check Digit Verification of cas no

The CAS Registry Mumber 2553-70-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,5 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2553-70:
(6*2)+(5*5)+(4*5)+(3*3)+(2*7)+(1*0)=80
80 % 10 = 0
So 2553-70-0 is a valid CAS Registry Number.

2553-70-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-sulfanylbenzene-1,3-diol

1.2 Other means of identification

Product number -
Other names 4-sulfanyl-1,3-benzenediol

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:2553-70-0 SDS

2553-70-0Relevant academic research and scientific papers

Ortho-Acidic aromatic thiols as efficient catalysts of intramolecular Morita-Baylis-Hillman and Rauhut-Currier reactions

Selig, Philipp S.,Miller, Scott J.

supporting information; experimental part, p. 2148 - 2151 (2011/05/05)

ortho-Mercaptobenzoic acid and ortho-mercaptophenols were discovered as efficient thiol catalysts of both the intramolecular Morita-Baylis-Hillman (MBH) and Rauhut-Currier (RC) reaction. High reaction rates were achieved under mildly basic, aqueous condit

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