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8H-indeno[1,2-d][1,2,3]thiadiazol-8-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87694-38-0

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87694-38-0 Usage

Properties

Heterocyclic organic compound, contains sulfur and nitrogen atoms in its ring structure, classified as a thioxanthone derivative

Potential Applications

Medicinal chemistry, materials science, organic synthesis

Uses

Photo-initiator in the production of photopolymer plates for printing
Sensitizing agent in photodynamic therapy for cancer treatment
Efficient and stable electron donor for organic solar cells

Unique Properties

Electronic and structural properties make it suitable for use in various applications

Versatile Chemical

Widely used in multiple industries for different purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 87694-38-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,9 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87694-38:
(7*8)+(6*7)+(5*6)+(4*9)+(3*4)+(2*3)+(1*8)=190
190 % 10 = 0
So 87694-38-0 is a valid CAS Registry Number.

87694-38-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name indeno[1,2-d]thiadiazol-4-one

1.2 Other means of identification

Product number -
Other names 8H-Indeno[1,2-d][1,2,3]thiadiazol-8-one

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:87694-38-0 SDS

87694-38-0Downstream Products

87694-38-0Relevant academic research and scientific papers

Influence of Benzo-bridging on the Stability of 6aλ4-Thia-1,2,5,6-tetraazapentalenic Systems

L'abbe, Gerrit,Dehaen, Wim,Bastin, Lieve,Declercq, Jean-Paul,Feneau-Dupont, J.

, p. 461 - 465 (2007/10/02)

Methylation of the phenylhydrazone derived from 8-oxo-8H-indeno-1,2,3-thiadiazole 5 with Meerwein's reagent furnishes the two methylated products 7 and 8.Single crystal X-ray analyses of these compounds reveal no significant S...NPh interaction, thus excluding a thiapentalene structure.

Sulfur Compounds in Crude Oil, III - Dihydrodiindenothiophenes

Boberg, Friedrich,Czogalla, Claus-Detlef,Torges, Karl-Franz,Wentrup, Gerhard-Juergen

, p. 1598 - 1607 (2007/10/02)

Syntheses to the dihydrodiindenothiophenes 1 - 3 have been studied. 1-3 were prepared by thermolysis of 8H-indeno-1,2,3-thiadiazole (10) or 4H-indeno-1,2,3-thiadiazole (13) or by reduction of the corresponding diketones 17, 19, and 21 which were obtained by thermolysis of indeno-1,2,3-thiadiazol-8-one (16) or from 2,3-dichloroinden-1-one (23) with Na2S.Mechanisms with analogous intermediates explain the formation of the indenothiophenes. - Another synthesis of indenothiophene-10,11-dione (21) starts from 2,5-diphenyl-3,4-thiophenedicarboxylic acid (29). - 10,11-Dihydrodiindenothiophene (3) is the known sulfurization product of hydrindene, the structure of 3 is corrected.

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