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18476-18-1

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18476-18-1 Usage

General Description

1,3,2-Benzodioxaphosphole, 2,2'-[1,3-propanediylbis(oxy)]bis- is a chemical compound that contains a phosphorus atom within a benzene ring. It is also known as bis(2,2'-[1,3-propanediylbis(oxy)])-1,3,2-benzodioxaphosphole. 1,3,2-Benzodioxaphosphole, 2,2'-[1,3-propanediylbis(oxy)]bis- has potential uses in coordination chemistry and as a ligand in organometallic complexes. It is used in the synthesis of various organophosphorus compounds and can also be used as a catalyst in organic reactions. The compound's unique structure and reactivity make it an important component in the development of new materials and chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 18476-18-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,7 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18476-18:
(7*1)+(6*8)+(5*4)+(4*7)+(3*6)+(2*1)+(1*8)=131
131 % 10 = 1
So 18476-18-1 is a valid CAS Registry Number.

18476-18-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[3-(1,3,2-benzodioxaphosphol-2-yloxy)propoxy]-1,3,2-benzodioxaphosphole

1.2 Other means of identification

Product number -
Other names -

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:18476-18-1 SDS

18476-18-1Downstream Products

18476-18-1Relevant articles and documents

EVIDENCE IN SUPPORT OF TETRAOXASPIROPHOSPHORANE INTERMEDIATES WITH A SIX-MEMBERED RING AND A P-H BOND IN INTRAMOLECULAR TRANSESTERIFICATION REACTIONS

Lier, Johan J. C. Van,Hermans, Rob J. M.,Buck, Henk M.

, p. 173 - 188 (2007/10/02)

Preparation of tetraoxaspirophosphorane 5 via two possible routes, starting from the isomeric P(V) precursors 10 and 11 results in identical 31P NMR spectra indicative of various P(III) compounds.By analysis of the products and application of low-temperature 31P NMR techniques it is shown that the phosphorane 5 is involved as an intermediate in the intramolecular transesterification 10 ->//- 28 which rules out spirophosphorane 7.These results are rationalized on the basis of orientation effects and Pearson's HASB theory.

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