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Phosphonic acid, [phenyl[(phenylmethyl)amino]methyl]-, diphenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63000-00-0

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63000-00-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63000-00-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,0 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 63000-00:
(7*6)+(6*3)+(5*0)+(4*0)+(3*0)+(2*0)+(1*0)=60
60 % 10 = 0
So 63000-00-0 is a valid CAS Registry Number.

63000-00-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-1-diphenoxyphosphoryl-1-phenylmethanamine

1.2 Other means of identification

Product number -
Other names diphenyl (benzylamino)(phenyl)methylphosphonate

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:63000-00-0 SDS

63000-00-0Downstream Products

63000-00-0Relevant academic research and scientific papers

Visible-Light Mediated Photooxidative Phosphorylation of Benzylamines: A Novel and Mild Pathway Towards α-Aminophosphorus Compounds

Ung, Sosthène P.-M.,Perepichka, Inna,Li, Chao-Jun

, (2021/12/09)

Traditional syntheses of α-aminophosphorus therapeutic targets proceed through the hydrophosphorylation of C=N or C=O bonds, thus necessitating preliminary oxidized substrates. Cross-dehydrogenative coupling strategies can bypass this extra oxidation step by oxidizing simpler substrates in situ before phosphorylating them, but those protocols can suffer from the use of toxic stoichiometric oxidants. Photochemical strategies can access those oxidized intermediates without any harsh conditions and can use molecular oxygen as a benign and sustainable oxidant. We report herein a simple protocol using visible light, phosphinylidenes and benzylamine derivatives for the synthesis of α-aminophosphorus products under aerobic conditions and using an iridium photosensitizer.

Efficient synthesis of α-aminophosphonates via one-pot reactions of aldehydes, amines, and phosphates in ionic liquid

Hajinasiri, Rahimeh,Hossaini, Zinatossadat,Rostami-Charati, Faramarz

experimental part, p. 625 - 629 (2011/12/04)

Ionic liquids such as 1,3-dialkylimidazolium bromides make excellent solvents for synthesis of α-aminophosphonates from aldehydes, amines, and phosphites. The ionic liquids are successfully regenerated and reused. Copyright

Facile synthesis of α-amino phosphonates in water by Kabachnik-Fields reaction using magnesium dodecyl sulfate

Ando, Kaori,Egami, Tomoe

experimental part, p. 358 - 362 (2012/01/06)

The three-component reaction of aldehydes, amines and triethyl or diphenyl phosphite was efficiently catalyzed by magnesium dodecyl sulfate at room temperature in water to give various α-amino phosphonates in high yields. The catalyst is easily available from inexpensive sodium dodecyl sulfate and magnesium bromide.

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