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72310-28-2

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72310-28-2 Usage

Description

2-CHLORONAPHTHO[1,8-D,E][1,3,2]DIOXAPHOSPHININE is a phosphorous-based chemical compound with the molecular formula C16H9ClO2P. It features a naphthalene ring with a chloro group attached, which contributes to its unique chemical structure and potential applications in various fields.

Uses

Used in Organic Chemistry:
2-CHLORONAPHTHO[1,8-D,E][1,3,2]DIOXAPHOSPHININE is used as a synthetic intermediate for the synthesis of complex organic molecules. Its unique structure allows it to be a valuable building block in the creation of new chemical entities.
Used in Materials Science:
In the field of materials science, 2-CHLORONAPHTHO[1,8-D,E][1,3,2]DIOXAPHOSPHININE may be utilized as a component in the development of advanced materials, taking advantage of its phosphorous-based composition and naphthalene ring system.
Used in Pharmaceutical Industry:
2-CHLORONAPHTHO[1,8-D,E][1,3,2]DIOXAPHOSPHININE is used as a potential candidate for drug discovery and development. Its unique chemical structure may offer novel interactions with biological targets, leading to the development of new therapeutic agents.
Used in Chemical Research:
2-CHLORONAPHTHO[1,8-D,E][1,3,2]DIOXAPHOSPHININE serves as a subject of study in chemical research, where its properties and reactivity can be explored to gain insights into new reaction mechanisms and the development of innovative synthetic methods.

Check Digit Verification of cas no

The CAS Registry Mumber 72310-28-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,3,1 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 72310-28:
(7*7)+(6*2)+(5*3)+(4*1)+(3*0)+(2*2)+(1*8)=92
92 % 10 = 2
So 72310-28-2 is a valid CAS Registry Number.

72310-28-2SDS

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 2-CHLORONAPHTHO[1,8-D,E][1,3,2]DIOXAPHOSPHININE

1.2 Other means of identification

Product number -
Other names 2-chloro-naphtho[1,8-de][1,3,2]dioxaphosphinine

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:72310-28-2 SDS

72310-28-2Upstream product

72310-28-2Downstream Products

72310-28-2Relevant articles and documents

Ring size effects in cyclic fluorophosphites: Ligands that span the bonding space between phosphites and PF3

Miles-Hobbs, Alexandra M.,Hunt, Eliza,Pringle, Paul. G.,Sparkes, Hazel A.

, p. 9712 - 9724 (2019/07/10)

The 5- to 8-membered cyclic fluorophosphites L5-8 have been prepared from the corresponding chlorophosphites which are derived from dihydroxyarenes or bis(trimethylsiloxy)arenes. Ligand L5 is very sensitive to hydrolysis but L6-8 are much more kinetically robust. The coordination chemistry of L5-8 has been explored with Mo(0), Pt(0) and Rh(i) and it is shown that the π-acceptor properties of L5-8 increase with decreasing ring size. The IR spectra and X-ray crystal structures of the [Mo(CO)4L2] complexes show that L5-8 lie between PF3 and P(OAr)3 in terms of their σ/π-bonding properties. The [PtL4] complexes are readily prepared from [Pt(nbe)3] and 4 equiv. of L5-8 whereas equilibrium mixtures of PtLx(nbe)y species form when 2 equiv. of L5-8 are added to [Pt(nbe)3]. The CO substitution reactions of [Rh2Cl2(CO)4] with L5-8 to give [Rh2Cl2L4] are evidence of the PF3-like ligand properties of L5-8. The trends in the properties of L5-8 are analysed in terms of their proximity to PF3 or P(OPh)3.

SYNTHESIS AND INVESTIGATION OF 1,8- AND 1,2-NAPHTHYLENE PHOSPHITES

Nifant'ev, E. E.,Milliaresi, E. E.,Ruchkina, N. G.,Druyan-Poleshchuk, L. M.,Vasyanina, L. K.,Tyan, E. A.

, p. 1295 - 1299 (2007/10/02)

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