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1,3,2-Dioxaphosphorinane, 2-(diphenylphosphino)-5,5-dimethyl-, 2-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54166-37-9

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54166-37-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54166-37-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,1,6 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54166-37:
(7*5)+(6*4)+(5*1)+(4*6)+(3*6)+(2*3)+(1*7)=119
119 % 10 = 9
So 54166-37-9 is a valid CAS Registry Number.

54166-37-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Diphenylphosphanyl-5,5-dimethyl-[1,3,2]dioxaphosphinane 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:54166-37-9 SDS

54166-37-9Upstream product

54166-37-9Downstream Products

54166-37-9Relevant academic research and scientific papers

Condensation reactions giving rise to P-P bonded compounds

Abraham, Kuzhikalail M.,Van Wazer, John R.

, p. 1099 - 1103 (2007/10/05)

The room-temperature condensation of CH3P(OCH3)2 with an equimolar amount of (C6H5)2PCl leads to the new compound (C6H5)2P-P(O)(CH3)OCH3, whereas the related reaction between CH3PCl2 and (C6H5)2POCH3 leads first to exchange of the chloro and methoxyl groups followed by slow self-condensation of the resulting CH3P(OCH3)Cl molecules. When CH3P(OCH3)2 is combined with an excess of (C6H5)2PCl, the product is found to react further with this excess reagent to give (C6H5)2P-P(C6H5) 2. Furthermore, the room-temperature reaction of CH3P(OCH3)2 with C6H5PCl2 leads to condensation products apparently based on the combination of the C6H5(CH3O)P- end group with CH3P(O)6H5P(O)3(CH3O)P(O)- group. The new compound (C6H5)2P-P(O)(OCH2) 2C(CH3)2 was obtained by reaction of (C6H5)2POCH3 with (CH3)2C(CH2O)2PCl, whereas, also at room temperature, only exchange of chloro for methoxyl group was observed in the reaction between o-C6H4O2PCl and (C6H5)2POCH3. At 140°, the reagents underwent exchange and condensation to give what appeared to be a P-O-P bridged structure, [C6H4O2P]2O.

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