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3775-15-3

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3775-15-3 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. Heterocyclic organic compound

Explanation

It is an organic compound containing a ring structure with atoms of different elements, in this case, carbon, nitrogen, and sulfur.
3. Five-membered ring

Explanation

The compound has a ring structure consisting of five atoms.
4. Contains sulfur and nitrogen atoms

Explanation

The ring structure includes a sulfur atom and two nitrogen atoms, which contribute to its unique properties.
5. Potential applications in organic synthesis and materials science

Explanation

The compound's structure and properties make it a useful building block for creating various organic compounds, including pharmaceuticals and agrochemicals.
6. Used as a building block in pharmaceuticals and agrochemicals

Explanation

Its unique structure allows it to be incorporated into the synthesis of various compounds used in the pharmaceutical and agrochemical industries.
7. Studied for potential as a corrosion inhibitor

Explanation

Research is being conducted to determine if the compound can be used to prevent or reduce the corrosion of metals.
8. Component in optoelectronic devices

Explanation

The compound's properties are being investigated for potential use in optoelectronic devices, which involve the interaction of light with electronic components.
9. Ongoing research

Explanation

Further studies are being conducted to better understand the properties and potential applications of 1,2,5-Thiadiazole, 3,4-diphenyl-, 1,1-dioxide.
10. Interest for chemists and materials scientists

Explanation

The compound's unique structure and potential applications make it an area of interest for researchers in the fields of chemistry and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 3775-15-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,7 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3775-15:
(6*3)+(5*7)+(4*7)+(3*5)+(2*1)+(1*5)=103
103 % 10 = 3
So 3775-15-3 is a valid CAS Registry Number.

3775-15-3SDS

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 3,4-diphenyl-1,2,5-thiadiazole 1,1-dioxide

1.2 Other means of identification

Product number -
Other names 3,4-diphenyl-1,2,5-thiadiazole-1,1-dioxide

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:3775-15-3 SDS

3775-15-3Relevant articles and documents

Reductive transformation of 3-methoxy-2-methyl-3,4-diphenyl-2,3-dihydro-1,2,5-thiadiazole 1,1-dioxide in the reaction with thiourea and HC1

Antonova, M. M.,Baranov, V. V.,Kravchenko, A. N.,Melnikova, E. K.

, p. 401 - 404 (2020/04/17)

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HETEROCYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

-

, (2019/09/06)

An organic light-emitting device and a heterocyclic compound, the device including a first electrode; a second electrode facing the first electrode; and an organic layer between the first electrode and the second electrode and including an emission layer, wherein the emission layer includes a compound represented by Formula 1A or a compound represented by Formula 1B:

Microwave-assisted synthesis of some substituted sulfamides

Gediz Erturk, Aliye,Bekdemir, Yunus

, p. 285 - 292 (2014/01/06)

Microwave-assisted synthesis of some substituted open-chain and cyclic sulfamides, by amine-exchange reaction, was studied in a modified domestic microwave oven. Reaction times and yields under microwave radiation were compared with classical heating. Synthesis of the sulfamides under microwave irradiation gave better yields with the desired compounds, and in considerably reduced reaction times, than those obtained by classical heating. [Supplementary materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfer, and Silicon and the Related Elements for the following free supplemental files: Additional figures.]

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