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Piperidine, 1-[(diphenylphosphinyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95038-61-2

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95038-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95038-61-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,0,3 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 95038-61:
(7*9)+(6*5)+(5*0)+(4*3)+(3*8)+(2*6)+(1*1)=142
142 % 10 = 2
So 95038-61-2 is a valid CAS Registry Number.

95038-61-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(diphenylphosphorylmethyl)piperidine

1.2 Other means of identification

Product number -
Other names (piperidin-1-ylmethyl)diphenylphosphine oxide

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:95038-61-2 SDS

95038-61-2Relevant academic research and scientific papers

Synthesis and biological activity of dialkylamino-substituted phosphine oxides

Yarkevich,Petrova,Bachurin

, p. 1659 - 1664 (2013/02/23)

A series of dialkylamino-substituted phosphine oxides was synthesized and their physiological activity was studied. Pleiades Publishing, Ltd., 2012.

The synthesis of α-amino-substituted diphenylphosphine oxides

Broekhof, N. L. J. M.,Elburg, P. van,Gen, A. van der

, p. 312 - 316 (2007/10/02)

Four methods with differing but overlapping specificity are described for the synthesis of α-unsubstituted as well as α-substituted (aminomethyl)diphenylphosphine oxides.The first method is based on the Arbusov reaction, the second on a Mannich-type condensation of diphenylphosphine oxide with aldehydes and secondary amines, the third on the addition of Ph2P(O)H to enamines and the fourth on the reaction of anions derived from α-unsubstituted (aminomethyl)diphenylphosphine oxides with various electrophiles.

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