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Diisopropyl (hydroxy(p-tolyl)Methyl)phosphonate is an organophosphorus compound known for its high thermal stability, low volatility, and excellent resistance to chemicals and weathering. It is commonly used in various applications due to its unique properties.

106736-84-9

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106736-84-9 Usage

Uses

Used in Polymer and Resin Production:
Diisopropyl (hydroxy(p-tolyl)Methyl)phosphonate is used as a flame retardant, plasticizer, and reactive diluent in the production of polymers and resins. Its properties contribute to enhancing the performance and safety of these materials.
Used in Pharmaceutical and Agrochemical Synthesis:
This chemical compound serves as an intermediate in the synthesis of pharmaceuticals and agrochemicals, playing a crucial role in the development of various medicinal and agricultural products.
Used in Engineering Plastics:
Diisopropyl (hydroxy(p-tolyl)Methyl)phosphonate is used as a flame retardant additive in engineering plastics, improving their fire resistance and safety characteristics.
Used in Polyurethane Foam Production:
In the production of polyurethane foam, diisopropyl (hydroxy(p-tolyl)Methyl)phosphonate is utilized as a flame retardant additive, enhancing the flame resistance of the final product.
Used in Production of Phosphorus-Containing Compounds:
Diisopropyl (hydroxy(p-tolyl)Methyl)phosphonate is also used as an intermediate in the production of phosphorus-containing compounds, which have various applications in different industries.
It is important to handle diisopropyl (hydroxy(p-tolyl)Methyl)phosphonate with caution, as it can be harmful if ingested, inhaled, or absorbed through the skin and may cause irritation to the eyes and skin.

Check Digit Verification of cas no

The CAS Registry Mumber 106736-84-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,7,3 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 106736-84:
(8*1)+(7*0)+(6*6)+(5*7)+(4*3)+(3*6)+(2*8)+(1*4)=129
129 % 10 = 9
So 106736-84-9 is a valid CAS Registry Number.

106736-84-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name diisopropyl (+/-)-[hydroxy(4-methylphenyl)methyl]phosphonate

1.2 Other means of identification

Product number -
Other names diisopropyl hydroxy(4-methylphenyl)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:106736-84-9 SDS

106736-84-9Relevant academic research and scientific papers

Cholic acid-alpha-amino phosphonate derivative and synthesis method thereof

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Paragraph 0015; 0016; 0026; 0030, (2016/10/09)

The invention belongs to the field of medicine chemistry and particularly relates to a cholic acid-alpha-amino phosphonate derivative and a preparation method thereof.Cholic acid and phosphate ester serve as raw materials, and the cholic acid-alpha-amino

Bile acid-alpha-hydroxyphosphonate derivatives and synthetic method thereof

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Paragraph 0017; 0018; 0020; 0022, (2016/12/22)

The invention belongs to the field of pharmaceutical chemistry and particularly relates to novel bile acid-alpha-hydroxyphosphonate compounds and a preparation method thereof. Bile acid and phosphate ester are taken as raw materials, the bile acid-alpha-h

Copper-catalyzed synthesis of α-hydroxy phosphonates from H-phosphonates and alcohols or ethers

Zhao, Zengxiang,Xue, Wanhua,Gao, Yuxing,Tang, Guo,Zhao, Yufen

supporting information, p. 713 - 716 (2013/05/09)

Easy PC: α-Hydroxy phosphonates were synthesized by copper/tert-butyl hydroperoxide (TBHP)-catalyzed oxidative addition reactions of H-phosphonates with alcohols or ethers. Diverse α-hydroxy phosphonates were obtained from substituted benzyl alcohols or alkyl alcohols and alkyl ethers in moderate to good yields. Copyright

Mechanistic approach for expeditious and solvent-free synthesis of α-hydroxy phosphonates using potassium phosphate as catalyst

Kulkarni, Makarand A.,Lad, Uday P.,Desai, Uday V.,Mitragotri, Satish D.,Wadgaonkar, Prakash P.

, p. 148 - 152 (2013/04/24)

An extremely simple, high yielding, highly rapid and solvent-free protocol has been described for hydrophosphylation of aldehydes using potassium phosphate as catalyst. Easy commercial availability of the reusable catalyst, operational simplicity at ambie

Asymmetric hydrogenation of α-keto phosphonates with chiral palladium catalysts

Goulioukina, Nataliya S.,Bondarenko, Grigorii N.,Bogdanov, Alexei V.,Gavrilov, Konstantin N.,Beletskaya, Irina P.

experimental part, p. 510 - 515 (2009/07/19)

Under atmospheric hydrogen pressure, a catalytic amount of palladium(II) trifluoroacetate and (R)-MeO-BIPHEP in 2,2,2-trifluoroethanol promoted the asymmetric hydrogenation of diisopropyl α-keto phosphonates 1 to afford the corresponding α-hydroxy phospho

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