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Naphtho[1,2-c][1,2,5]thiadiazole is a heterocyclic organic compound with the molecular formula C10H5N3S. It is a derivative of naphthalene, featuring a thiadiazole ring fused to the naphthalene core. Naphtho[1,2-c][1,2,5]thiadiazole is known for its potential applications in the synthesis of various pharmaceuticals, agrochemicals, and materials science due to its unique electronic properties and chemical reactivity. The structure of naphtho[1,2-c][1,2,5]thiadiazole consists of a naphthalene ring with a sulfur atom and two nitrogen atoms forming a thiadiazole ring attached to the first and second carbon atoms of the naphthalene. Naphtho[1,2-c][1,2,5]thiadiazole can be synthesized through various methods, including cyclization reactions, and is often used as a building block in the development of new compounds with specific properties.

233-68-1

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233-68-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 233-68-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,3 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 233-68:
(5*2)+(4*3)+(3*3)+(2*6)+(1*8)=51
51 % 10 = 1
So 233-68-1 is a valid CAS Registry Number.

233-68-1SDS

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 benzo[g][2,1,3]benzothiadiazole

1.2 Other means of identification

Product number -
Other names Naphtho<1,2-d>2,1,3>AC1LG3NV

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:233-68-1 SDS

233-68-1Relevant academic research and scientific papers

Sulfur Nitride in Organic Chemistry. Part 19. Selective Formation of Benzo- and Benzobisthiadiazole Skeleton in the Reaction of Tetrasulfur Tetranitride with Naphthalenols and Related Compounds

Mataka, Shuntaro,Takahashi, Kazufumi,Ikezaki, Youji,Hatta, Taizo,Tori-i, Akiyoshi,Tashiro, Masashi

, p. 68 - 73 (2007/10/02)

Tetrasulfur tetranitride (N4S4) reacted with 2-naphthols to afford naphthothiadiazoles (13) in high yields, while 1-naphthols gave naphtholbisthiadiazoles as a major product, together with a small amount of 13.In the reactions with naphthalenediols such as 1,5-, 2,6-, 2,7-, 1,6-, and 1,7-diol, naphtho- or naphthobisthiadiazoles were obtained in varying yields.In some cases, naphthotristhiadiazole was formed as a by-product.In reaction with 5-isoquinolinol, 8-quinolinoles,9H-carbazol-2-ol, and dibenzofuran-2-ol, one and/or two 1,2,5-thiadiazole-ringfused heteroaromatic compounds were obtained.

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