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2-(dimethylphosphoryl)isonicotinic acid is a versatile chemical compound characterized by the presence of a phosphoryl group attached to a dimethyl group and an isonicotinic acid molecule. It exhibits a range of chemical properties and reactivity, making it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and various organic compounds. Its potential applications span across medicine, agriculture, and material science, with ongoing research exploring its biological activities and therapeutic effects.

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  • 1508339-39-6 Structure
  • Basic information

    1. Product Name: 2-(dimethylphosphoryl)isonicotinic acid
    2. Synonyms:
    3. CAS NO:1508339-39-6
    4. Molecular Formula:
    5. Molecular Weight: 199.146
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1508339-39-6.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: 2-(dimethylphosphoryl)isonicotinic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(dimethylphosphoryl)isonicotinic acid(1508339-39-6)
    11. EPA Substance Registry System: 2-(dimethylphosphoryl)isonicotinic acid(1508339-39-6)
  • 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: 1508339-39-6(Hazardous Substances Data)

1508339-39-6 Usage

Uses

Used in Pharmaceutical Industry:
2-(dimethylphosphoryl)isonicotinic acid serves as a crucial intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique chemical structure allows for the creation of compounds with specific biological activities, enhancing the effectiveness of medications and expanding treatment options for various diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(dimethylphosphoryl)isonicotinic acid is utilized as a building block for the production of pesticides, herbicides, and other crop protection agents. Its incorporation into these compounds can improve their efficacy, selectivity, and environmental compatibility, ensuring sustainable agricultural practices and crop yield protection.
Used in Material Science:
2-(dimethylphosphoryl)isonicotinic acid also finds applications in material science, where it can be used to develop novel materials with specific properties. Its reactivity and chemical versatility enable the synthesis of advanced materials for various applications, such as sensors, catalysts, and functional coatings.
Used in Research and Development:
Due to its diverse chemical properties and potential therapeutic effects, 2-(dimethylphosphoryl)isonicotinic acid is a subject of interest for further research and development. Scientists and researchers are exploring its biological activities, aiming to uncover new applications and enhance its potential in various fields, including medicine, agriculture, and material science.

Check Digit Verification of cas no

The CAS Registry Mumber 1508339-39-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,0,8,3,3 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1508339-39:
(9*1)+(8*5)+(7*0)+(6*8)+(5*3)+(4*3)+(3*9)+(2*3)+(1*9)=166
166 % 10 = 6
So 1508339-39-6 is a valid CAS Registry Number.

1508339-39-6Downstream Products

1508339-39-6Relevant articles and documents

Phosphine Oxides (-POMe2) for Medicinal Chemistry: Synthesis, Properties, and Applications

Stambirskyi, Maksym V.,Kostiuk, Tetiana,Sirobaba, Serhii I.,Rudnichenko, Alexander,Titikaiev, Dmytro L.,Dmytriv, Yurii V.,Kuznietsova, Halyna,Pishel, Iryna,Borysko, Petro,Mykhailiuk, Pavel K.

, p. 12783 - 12801 (2021/09/18)

A general practical approach to hetero(aromatic) and aliphatic P(O)Me2-substituted derivatives is elaborated. The key synthetic step was a [Pd]-mediated C-P coupling of (hetero)aryl bromides/iodides with HP(O)Me2. The P(O)Me2 substituent was shown to dramatically increase solubility and decrease lipophilicity of organic compounds. This tactic was used to improve the solubility of the antihypertensive drug prazosin without affecting its biological profile.

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