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(4-dimethylamino-phenyl)-phosphonous acid dichloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 29972-74-5 Structure
  • Basic information

    1. Product Name: (4-dimethylamino-phenyl)-phosphonous acid dichloride
    2. Synonyms: (4-dimethylamino-phenyl)-phosphonous acid dichloride
    3. CAS NO:29972-74-5
    4. Molecular Formula:
    5. Molecular Weight: 222.054
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 29972-74-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (4-dimethylamino-phenyl)-phosphonous acid dichloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4-dimethylamino-phenyl)-phosphonous acid dichloride(29972-74-5)
    11. EPA Substance Registry System: (4-dimethylamino-phenyl)-phosphonous acid dichloride(29972-74-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 29972-74-5(Hazardous Substances Data)

29972-74-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 29972-74-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,9,7 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 29972-74:
(7*2)+(6*9)+(5*9)+(4*7)+(3*2)+(2*7)+(1*4)=165
165 % 10 = 5
So 29972-74-5 is a valid CAS Registry Number.

29972-74-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name dichloro(4-N,N-dimethylaminophenyl)phosphine

1.2 Other means of identification

Product number -
Other names 4-dichlorophosphino-N,N-dimethyl-aniline

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:29972-74-5 SDS

29972-74-5Relevant articles and documents

Reactive intermediates: A transient electrophilic phosphinidene caught in the act

Jansen, Helen,Samuels, Michiel C.,Couzijn, Erik P.A.,Slootweg, J. Chris,Ehlers, Andreas W.,Chen, Peter,Lammertsma, Koop

, p. 1454 - 1458 (2010)

Trapped! Transient electrophilic phosphinidenes [R-P=W(CO)5] have emerged as versatile intermediates that are highly valuable in the synthesis of a plethora of organophosphorus compounds, nevertheless their existence has never been unequivocall

The Formation of P-C Bonds Utilizing Organozinc Reagents for the Synthesis of Aryl- A nd Heteroaryl-Dichlorophosphines

Kirst, Christin,Tietze, Jonathan,Ebeling, Marian,Horndasch, Lukas,Karaghiosoff, Konstantin

, p. 17337 - 17343 (2021/11/18)

Aryl- A nd heteroaryl-dichlorophosphines are mildly and selectively made in a one-pot synthesis in moderate to good yields starting from the respective aryl bromides or five-membered heterocycles, following lithiation with nBuLi, transmetalation with ZnCl

Metal control of non-polar binding shape selectivity

Wang, Fen,Schwabacher, Alan W.

, p. 7641 - 7644 (2007/10/03)

Ligand 1 forms a hydrophobic cavity upon binding to metals, the shape of which depends on the metal. A reversal in binding preference for naphthalene or biphenyl groups is found when the metal is changed from zinc to copper, with a selectivity change of 260 fold.

Tuning of Binding Selectivity: Metal Control of Organic Guest Binding and Allosteric Perturbation of Fluorescent Metal Sensor

Wang, Fen,Schwabacher, Alan W.

, p. 8922 - 8928 (2007/10/03)

Ligand 1, bearing two ethylenediamine groups, was designed to form a Hydrophobic cavity upon binding to metals. The shape of its nonpolar cavity depends on the metal: a reversal in binding preference for naphthalene or biphenyl groups is found when the metal is changed from zinc to copper, with a selectivity change of 260-fold. In the presence of dansylated amino acids, the new ligand constitutes a fluorescent sensor for zinc ion. Variations are seen in affinity for dansylamino acid with minor structural changes, and organic selectivity changes with complexes of variant metals. These findings suggest that sensor tuning of affinity and selectivity for metal is possible by choice of simple organic guest and for organic guest by choice of metal.

The kinetics and mechanism of the reaction of tricoordinate phosphorus compounds with sulfenate esters

Hall, C. Dennis,Tweedy, Bruce R.,Lowther, Nicholas

, p. 341 - 358 (2007/10/03)

The kinetics and mechanism of the reaction of tricoordinate phosphorus compounds, ArnP(OCH2CF3)3-n with arylsulfenate esters, ArSOCH2CF3, are reported. Product analysis, kinetic order, activation parameters, Hammett data and solvent effects are the criteria used to elucidate the two step mechanism involving arylthiophosphoranes as intermediates.

Effect of para Substituents on Decomposition Rates of 2-(N,N'-Dimethylamino)ethyl Phenyl Phenylphosphonates

Manninen, P. Antti

, p. 635 - 640 (2007/10/02)

Spontaneous decomposition of nineteen of the title phosphonates to their 1,1,4,4-tetramethylpiperazinium salts was followed in 50 percent aqueous ethanol at different temperatures.The effect of substituents of the phenyl group on reaction rates was about

SYNTHESIS OF PHOSPHONIC DICHLORIDES AND CORRELATION OF THEIR P-31 CHEMICAL SHIFTS

Grabiak, Raymond C.,Miles, James A.,Schwenzer, Gretchen M.

, p. 197 - 202 (2007/10/02)

Various mono-substituted diethyl arylphosphonates were prepared in good yield by treatment of aryl bromides or iodides with triethyl phosphite in the presence of NiCl2 or alternatively, addition of the aryl grignard reagent to diethyl phosphorochloridate.

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