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1,2-Azaphosphorine, 1-(1,1-dimethylethyl)-1,2-dihydro-3,5-dimethyl-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111077-76-0

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111077-76-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111077-76-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,0,7 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 111077-76:
(8*1)+(7*1)+(6*1)+(5*0)+(4*7)+(3*7)+(2*7)+(1*6)=90
90 % 10 = 0
So 111077-76-0 is a valid CAS Registry Number.

111077-76-0SDS

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 1-tert-butyl-3,5-dimethyl-2-phenyl-1,2-dihydro-1,2-λ3-azaphosphinine

1.2 Other means of identification

Product number -
Other names 1-tert-butyl-3,5-dimethyl-2-phenyl-1,2-dihydro-1,2λ3-azaphosphinine

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:111077-76-0 SDS

111077-76-0Relevant academic research and scientific papers

REACTIONS DE LA DICHLOROPHENYLPHOSPHINE AVEC LES IMINES: SYNTHESE DES DIHYDRO-1,2 λ3-AZAPHOSPHININES-1,2 ET DES OXO-2 AZAPHOSPHOLENES-1,2,4

Tan, Wai He-Line Wai,Bourdieu, Catherine,Foucaud, Andre

, p. 6715 - 6730 (2007/10/02)

The reaction of one equivalent of dichlorophenylphosphine with two equivalents of aliphatic imines gives a mixture of 1,2-dihydro 1,2 λ3-azaphosphinines 2 and 2-oxo 1,2,4-azaphospholenes 3.Compounds 2 are the major product when the imines are prepared from amines with bulky group.The yield of azaphospholenes 3 is enhanced when the dichlorophenylphosphine is used in excess.Oxidation of azaphosphinines 2 with hydrogen peroxide gives 2-oxo 1,2-azaphosphinines 4.

SYNTHESIS OF THE 1,2-DIHYDRO 1,2-λ3-AZAPHOSPHORINES

Bourdieu, Catherine,Foucaud, Andre

, p. 365 - 368 (2007/10/02)

1,2-Dihydro 1,2-λ3-azaphosphorines were prepared by reaction of dichlorophenylphosphine with two equivalents of imines. 2-Oxo 1,2-azaphospholenes were also obtained in some cases.

FIRST SYNTHESIS OF 1,2-DIHYDRO 1,2-λ3-AZAPHOSPHORINES

Bourdieu, Catherine,Foucaud, Andre

, p. 4725 - 4726 (2007/10/02)

1,2-dihydro 1,2-λ3-azaphosphorines were prepared by reaction of dichlorophenylphosphine with two equivalents of imines derived from propanal.In some cases, 2-oxo 1,2-azaphospholenes were also obtained.

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