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Phosphonic diamide, N,N'-dimethyl-P-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14360-84-0

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14360-84-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14360-84-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,6 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14360-84:
(7*1)+(6*4)+(5*3)+(4*6)+(3*0)+(2*8)+(1*4)=90
90 % 10 = 0
So 14360-84-0 is a valid CAS Registry Number.

14360-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-dimethyl-P-phenylphosphonic diamide

1.2 Other means of identification

Product number -
Other names Phenylphosphonic acid bis(N-methylamide)

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:14360-84-0 SDS

14360-84-0Downstream Products

14360-84-0Relevant academic research and scientific papers

Alpha- haloenamine reagents

-

, (2008/06/13)

The present invention describes immobilized haloenamine reagents, immobilized tertiary amides, methods for their preparation, and methods of use.

N-(Alkylphenylphosphinoyl)hydroxylamines: Highly Selective Migration of the Phenyl Group in the Base-induced Rearrangement of their O-Methylsulphonyl Derivatives

Harger, Martin J. P.,Smith, Adrian

, p. 683 - 688 (2007/10/02)

The N-(alkylphenylphosphinoyl)hydroxylamines RPh(O)NHOH (R=Me, Et, or Pri) have been prepared and converted into their O-methylsulphonyl derivatives RPhP(O)NHOMs.These readily rearrange on treatment with methylamine, t-butylamine, or sodium methoxide-methanol to give only the products RP(O)(NHPh)X (X=NHMe, NHBut, or OMe) resulting from migration of the phenyl group.The rates of reaction are essentially the same when R=Me and R=Pri, indicating that the rearrangement is not brought about by nucleophilic attack at phosphorus.A likely mechanism involves base-induced rearrangement to a monomeric metaphosphonimidate which then reacts rapidly with the nucleophile.

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