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1,3,2-Dioxaphospholane, 4,4,5,5-tetramethyl-2-(phenylmethoxy)-, 2-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

113612-67-2

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113612-67-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113612-67-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,6,1 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 113612-67:
(8*1)+(7*1)+(6*3)+(5*6)+(4*1)+(3*2)+(2*6)+(1*7)=92
92 % 10 = 2
So 113612-67-2 is a valid CAS Registry Number.

113612-67-2SDS

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-Benzyloxy-4,4,5,5-tetramethyl-[1,3,2]dioxaphospholane 2-oxide

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:113612-67-2 SDS

113612-67-2Downstream Products

113612-67-2Relevant academic research and scientific papers

1H-Tetrazole Catalysed Reactions of Trialkyl Phosphites: Observation of a Five-membered Cyclic Hydrophosphorane Intermediate during the Transesterification

Watanabe, Yutaka,Maehara, Shin-ichi,Ozaki, Shoichiro

, p. 1879 - 1880 (2007/10/02)

1H-Tetrazole-catalysed transesterification of a trialkyl phosphite with an alcohol and a (31)P NMR experiment in the case of 4,4,5,5-tetramethyl-2-(3-phenylpropoxy)-1,3,2-dioxaphospholane showed the existence of the corresponding cyclic five-coordinate hydrophosphorane as an intermediate.

SYNTHESE ET REACTIVITE D'UN ESTER CYCLIQUE D'α-AMINODIPHOSPHONATE. II.

Burgada, R.,Manouni, D. El,Tromelin, A.,Fauduet, H.

, p. 275 - 282 (2007/10/02)

The reactions of methoxy dioxaphospholan and corresponding hydrogen phosphonate 1 with (MeN=CHCl)Cl, (MeO)2CHNMe2 and MeOCH2NMe2 have been studied.These reactions lead either to amino diphosphonate 5 or to amino phosphonate 3 and phosphate 2.The hydrolysi

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