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1,2-Diphenyl-2,3-dihydro-1H-1,3,2-benzodiazaphosphole 2-sulfide is a complex organic compound with the molecular formula C19H16NPS. It is a derivative of benzodiazaphosphole, which is a heterocyclic compound containing a phosphorus atom. This specific compound features two phenyl groups attached to the first and second carbon atoms, a dihydro structure, and a sulfide group at the 2-position. It is known for its potential applications in the field of pharmaceuticals and materials science, particularly as a precursor in the synthesis of various biologically active molecules and as a ligand in coordination chemistry. The compound's structure and properties make it a subject of interest for researchers exploring new compounds with unique reactivity and potential therapeutic applications.

4601-98-3

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4601-98-3 Usage

Explanation

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

Explanation

The compound's structure consists of a benzodiazaphosphole ring, which is a fused ring system containing a benzene ring and a diazaphosphole ring. Two phenyl groups are attached to the benzene ring, and a sulfur atom is attached to the diazaphosphole ring.

Explanation

The compound is classified as a phosphine-sulfide due to the presence of both phosphorus and sulfur atoms in its structure.

Explanation

1,2-diphenyl-2,3-dihydro-1H-1,3,2-benzodiazaphosphole 2-sulfide can be used as a ligand, which is a molecule that binds to a metal center in a complex to form a coordination complex.

Explanation

The compound has been studied for its potential use in catalysis, which is the acceleration of a chemical reaction by a substance that remains unchanged after the reaction. It is also considered as an intermediate in the synthesis of other organic compounds, which are used in various industries and applications.

Explanation

The compound's unique structure and properties make it an interesting subject for research in the field of organic chemistry. Its potential applications in catalysis and as an intermediate in the synthesis of other organic compounds contribute to its practical value in the field.

Structure

Benzodiazaphosphole ring with two phenyl groups and a sulfur atom attached

Type of compound

Phosphine-sulfide

Application

Ligand in organometallic chemistry reactions

Potential applications

Catalysis and synthesis of other organic compounds

Unique structure and properties

Valuable for research and practical applications in organic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 4601-98-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,0 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4601-98:
(6*4)+(5*6)+(4*0)+(3*1)+(2*9)+(1*8)=83
83 % 10 = 3
So 4601-98-3 is a valid CAS Registry Number.

4601-98-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-diphenyl-2-sulfanylidene-1H-1,3,2λ<sup>5</sup>-benzodiazaphosphole

1.2 Other means of identification

Product number -
Other names 1,2-diphenyl-2,3-dihydro-1H-benzo[1,3,2]diazaphosphole 2-sulfide

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:4601-98-3 SDS

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