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2-phenyl-2,3-dihydro-1H-1,3,2-benzodiazaphosphole 2-oxide is a complex organic compound belonging to the class of benzodiazaphospholes. It is characterized by a unique structure that includes a benzene ring fused to a diazaphosphole ring, with the latter containing a phosphorus atom. The compound is further defined by the presence of a phenyl group attached to the benzene ring and a 2-oxide functional group, which indicates the presence of an oxygen atom double-bonded to the phosphorus. This specific arrangement of atoms and functional groups endows the compound with distinct chemical properties and potential applications in various fields, such as pharmaceuticals or materials science.

7597-43-5

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7597-43-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7597-43-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,9 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7597-43:
(6*7)+(5*5)+(4*9)+(3*7)+(2*4)+(1*3)=135
135 % 10 = 5
So 7597-43-5 is a valid CAS Registry Number.

7597-43-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-1,3-dihydro-1,3,2λ<sup>5</sup>-benzodiazaphosphole 2-oxide

1.2 Other means of identification

Product number -
Other names 1H-1,2-Benzodiazaphosphole,2,3-dihydro-2-phenyl-,2-oxide

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:7597-43-5 SDS

7597-43-5Downstream Products

7597-43-5Relevant academic research and scientific papers

Microwave-assisted synthesis and diabetic/antioxidant assessments of 1,3,2-benzothiazaphosphole-3(2H)-carbothioamide- and -diazaphosphole-3(2H)-dicarbothioamide 2-oxide derivatives

Abdou, Wafaa M.,Bekheit, Mohamed S.,Barghash, Reham F.

, p. 1797 - 1808 (2016)

Abstract: Environmentally friendly synthesis of 1,3,2-benzothiazaphosphole-3(2H)-carbothioamide and -diazaphosphole-3(2H)-dicarbothioamide 2-oxides or the carboxamide 2-oxide analogs was reported. The targets were accomplished via a two step process: (1) preparation of the substrates 2-phenyl-2,3-dihydro-1H-1,3,2-benzothiazaphosphole 2-oxide and -1,3,2-benzodiazaphosphole 2-oxide; (2) exploiting these two phospholes in reactions with various saturated and unsaturated isothiocyanates and some isocyanate analogs in dry DMF/pyridine under microwave irradiation thereby isolating the target compounds in 85–95?% yields. Based upon computer-assisted molecular model (CAMM), new compounds were screened for their antidiabetic and antioxidant properties and many of them exhibited moderate to high in vivo and in vitro diabetic and/or antioxidant potencies. Graphical abstract: [Figure not available: see fulltext.]

Five- and Six-Membered Cyclic Phosphonic Diamides, Thioester-amides and Spirobi

Neidlein, Richard,Buseck, Stephan

, p. 2520 - 2530 (2007/10/02)

By reaction of the 1,2-diaminobenzene derivatives 1a-d with the phosphonyl dichlorides 2a-g, the 1,3-dihydro-1,3,2-benzodiazaphosphol-2-ones 4a-q are obtained.The phosphonoyl dichlorides 2a-e, 2g, and 2h yield with naphthalene-1,8-diamines (5) the diazaph

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