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17534-14-4

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17534-14-4 Usage

General Description

Anthracene-9-thiol is a chemical compound with the molecular formula C14H10S. It is a derivative of anthracene, a polycyclic aromatic hydrocarbon. Anthracene-9-thiol is a yellow to brown solid that is insoluble in water but soluble in organic solvents. It is primarily used as a building block for the synthesis of various organic compounds, including dyes, pigments, and pharmaceuticals. Anthracene-9-thiol has also been studied for its potential use in organic photovoltaic devices due to its strong absorption in the visible region of the electromagnetic spectrum. It can also be used as a fluorescent probe for the detection of metallic ions. However, it is important to handle anthracene-9-thiol with care as it is a skin and respiratory irritant and may be harmful if swallowed or inhaled.

Check Digit Verification of cas no

The CAS Registry Mumber 17534-14-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,3 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 17534-14:
(7*1)+(6*7)+(5*5)+(4*3)+(3*4)+(2*1)+(1*4)=104
104 % 10 = 4
So 17534-14-4 is a valid CAS Registry Number.

17534-14-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name anthracene-9-thiol

1.2 Other means of identification

Product number -
Other names 9-Thioanthrol

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:17534-14-4 SDS

17534-14-4Relevant articles and documents

Cycloadditions. 23. The Thermal Reactivity of S-(1-Naphthyl) and S-(9-Anthryl)-2-methyl-2,3-butadienethioates

Himbert, Gerhard,Fink, Dieter

, p. 654 - 657 (1994)

Heating of the S-(1-naphthyl)esters of 2-methyl-2,3-butadiene thioacid and of 2-methyl-4,4-diphenyl-2,3-butadiene thioacid (3a resp. 3b) furnishes mixtures of the Diels-Alder products 5a,b and the cyclobutenone 7 and the naphthol derivative 8, resp.The corresponding S-(9-anthryl)esters 4a,b are not isolable; under the conditions of their synthesis (allenecarboxylic acids 1a u. b, 9-thioanthrol 2b, DCC and DMAP) they isomerise spontaneously to the Diels-Alder products 9.

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