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3283-12-3

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3283-12-3 Usage

Description

Dimethylphosphinic acid, a white crystalline compound, is an organophosphorus compound with the chemical formula (CH3)2PHO2H. It is known for its unique chemical properties and ability to form hydrogen-bonded cyclic dimers. The molecular structure of this compound has been studied using gas-phase electron diffraction at various temperatures, including 433K.

Uses

Used in Chemical Synthesis:
Dimethylphosphinic acid is used as a key intermediate in the synthesis of various organophosphorus compounds, including organometallic coordination polymers. Its unique chemical properties make it a valuable building block for creating complex molecular structures with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, dimethylphosphinic acid may be utilized as a precursor for the development of new drugs or drug candidates. Its ability to form stable complexes with metal ions can be exploited to design novel therapeutic agents with improved pharmacological properties.
Used in Material Science:
Dimethylphosphinic acid can be employed in the preparation of microcrystalline organometallic coordination polymers, which have potential applications in various fields, such as catalysis, gas storage, and electronic devices. These coordination polymers can exhibit unique properties due to their metal-organic framework (MOF) structures, making them attractive for research and development.
Used in Analytical Chemistry:
The infrared spectra of dimethylphosphinic acid, both in gaseous and polycrystalline forms, can be used for analytical purposes. Understanding the vibrational modes and bonding characteristics of this compound can provide valuable insights into its chemical behavior and potential interactions with other molecules, which can be useful in various analytical techniques.

Check Digit Verification of cas no

The CAS Registry Mumber 3283-12-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,8 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3283-12:
(6*3)+(5*2)+(4*8)+(3*3)+(2*1)+(1*2)=73
73 % 10 = 3
So 3283-12-3 is a valid CAS Registry Number.
InChI:InChI=1/C2H7O2P/c1-4-5(2)3/h5H,1-2H3

3283-12-3 Well-known Company Product Price

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  • Aldrich

  • (328294)  Dimethylphosphinicacid  97%

  • 3283-12-3

  • 328294-100MG

  • 558.09CNY

  • Detail
  • Aldrich

  • (328294)  Dimethylphosphinicacid  97%

  • 3283-12-3

  • 328294-500MG

  • 1,838.07CNY

  • Detail

3283-12-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethylphosphinic acid

1.2 Other means of identification

Product number -
Other names Phosphinic acid, dimethyl-

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:3283-12-3 SDS

3283-12-3Relevant articles and documents

Broad spectrum catalytic system for the deep oxidation of toxic organics in aqueous medium using dioxygen as the oxidant

Pifer, Anne,Hogan, Terrence,Snedeker, Benjamin,Simpson, Robert,Lin, Minren,Shen, Chengyu,Sen, Ayusman

, p. 7485 - 7492 (1999)

In water, metallic palladium was found to catalyze the deep oxidation of a wide variety of functional organics by dioxygen at 80-90°C in the presence of carbon monoxide or dihydrogen. Several classes of organic compounds were examined: benzene, phenol and substituted phenols, nitro and halo organics, organophosphorus, and organosulfur compounds. In every case, deep oxidation to carbon monoxide, carbon dioxide, and water occurred in high yields, resulting in up to several hundred turnovers over a 24 h period. For substrates susceptible to hydrogenation, the conversions were generally higher with dihydrogen than with carbon monoxide. For organophosphorus compounds, the system presents the first examples of catalytic cleavage of phosphorus - alkyl bonds.

A dimethyl secondary phosphate preparation method and its product and application (by machine translation)

-

Paragraph 0040; 0041, (2017/03/14)

The invention discloses a method for preparing dimethyl hypophosphite, first, the halogenated methane and methyl dimethyl phosphite according to mol ratio of 0.1-10:100 mixed, 90-150 °C reaction under 4-6h, be dimethyl phosphinic acid methyl ester; and then the the dimethyl phosphinic acid methyl ester mix with deionized water, the 80-120 °C hydrolysis reaction under acidic conditions 6-8h, be dimethyl phosphinic acid; soluble salt of the metal with the dimethyl phosphinic acid mixing, reaction to obtain the precipitate, then post-processed to obtain dimethyl hypophosphite; the metal as Al, Zn, Ti, Ca, mg or Fe. The invention also discloses the method the prepared dimethyl hypophosphite, has higher phosphorus content, will be applied to the engineering plastic, especially in glass fiber reinforced nylon and glass fiber reinforced polyester will obtain better fire retardant effect. (by machine translation)

COMPOSITIONS AND METHODS FOR TREATING CANCER

-

, (2012/12/13)

The instant invention provides a method of treating a cancer selected from the group consisting of non-small cell lung cancer and breast cancer with an mTOR inhibitor and an αvβ3 integrin antagonist, wherein the mTOR inhibitor is ridaforolimus, everolimus, temsirolimus or a combination thereof.

Phosphorus-containing compounds and uses thereof

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, (2008/06/13)

This invention concerns a new family of phosphorus-containing compounds containing a moiety JQA—in which: A is absent or is —O—, —S— or —NR2—; Q is absent or (if A is —O—, —S— or —NR2—) Q may be —V—, —OV—, —SV—, or —NR2V—, where V is an aliphatic, heteroaliphatic, aryl, or heteroaryl moiety, such that J is linked to the cyclohexyl ring directly, through A or through VA, OVA, SVA or NR2VA; K is O or S; each occurrence of Y is independently —O—, —S—, —NR2—, or a chemical bond linking a R5 moiety to P; and the other variables are as defined herein.

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