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1,3,2-Benzodioxaphosphole, 2-(phenylmethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69626-77-3

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69626-77-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69626-77-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,6,2 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 69626-77:
(7*6)+(6*9)+(5*6)+(4*2)+(3*6)+(2*7)+(1*7)=173
173 % 10 = 3
So 69626-77-3 is a valid CAS Registry Number.

69626-77-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenylmethoxy-1,3,2-benzodioxaphosphole

1.2 Other means of identification

Product number -
Other names 2-benzyloxy-4,5-benzo-1,3,2-dioxaphospholane

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:69626-77-3 SDS

69626-77-3Relevant academic research and scientific papers

Structure-property-reactivity studies on dithiaphospholes

Ould, Darren M. C.,Tran, Thao T. P.,Rawson, Jeremy M.,Melen, Rebecca L.

, p. 16922 - 16935 (2019/11/26)

The reaction of either toluene-3,4-dithiol or benzene dithiol with phosphorus(iii) trihalides generates the corresponding benzo-fused 1,3,2-dithiaphospholes, RC6H3S2PX (R = Me (1), R = H (2); X = Cl, Br, I). The P-chloro-dithiaphospholes undergo: (a) halogen abstraction reactions with Lewis acids forming phosphenium cations; (b) substitution with LiHMDS base and; (c) reduction chemistry with sodium metal to generate the P-P σ-bonded dimer, (RC6H3S2P)2. Reduction catalysis of aldehydes with pinacolborane using dithiaphospholes is compared with their dioxaphosphole and diazaphosphole counterparts as pre-catalysts, revealing interesting differences in the reactivity of this series of compounds.

Syntheses und NMR-Spektren phosphororganischer Antioxidantien und verwandter Verbindungen

Koenig, T.,Habicher, W.D.,Haehner, U.,Pionteck, J.,Rueger, C.,Schwetlick, K.

, p. 333 - 349 (2007/10/02)

The syntheses of various aliphatic, aromatic, sterically hindered, and cyclic organophosphorus compounds (phosphorous acid esters, esters chlorides and ester amides, hydrogen phosphites, phosphinates and phosphates) are reported, and general procedures for preparation are given.The compounds synthesized were investigated by means of 31P-, 1H- and 13C-n.m.r. spectroscopy, and the chemical shifts measured are listed.

REACTIONS OF P(III) THIOBENZYL ESTERS WITH METHYL IODIDE

Burilov, A. R.,Drozdova, Ya. A.,Pudovik, M. A.,Pudovik, A. N.

, p. 2491 - 2492 (2007/10/02)

The reactions of S-benzyl diphenylthiophosphinite and 2-benzylthio-4,5-benzo-1,3,2-dioxaphospholane with methyl iodide have been examined.In contrast to the oxygen analogs, the reaction occurs under mild conditions, and does not give Arbuzov reaction products.

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