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Methyl 4-iodopyridine-2-carboxylate is a complex organic compound belonging to the class of pyridines and derivatives. It features an iodine atom and a methyl group attached to a pyridine ring, classifying it as a halogenated derivative. With a chemical formula of C7H6INO2, this light-sensitive material necessitates careful storage and handling. Known by its IUPAC name, methyl 4-iodo-2-pyridinecarboxylate, it is widely utilized in chemical research and industrial processes as a reagent or intermediate for synthesizing other compounds.

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  • 380381-28-2 Structure
  • Basic information

    1. Product Name: Methyl 4-iodopyridine-2-carboxylate
    2. Synonyms: METHYL 4-IODOPYRIDINE-2-CARBOXYLATE 98%METHYL 4-IODOPICOLINATE;Methyl 4-iodopyridine-2-carboxylate 98%;Methyl 4-iodopyridine-2-carboxylate;Methyl-ioddopicolinate;Methyl4-iodopyridine-2-carboxylate98%
    3. CAS NO:380381-28-2
    4. Molecular Formula: C7H6INO2
    5. Molecular Weight: 263.03
    6. EINECS: N/A
    7. Product Categories: blocks;Carboxes;Iodides;Pyridines;Pyridine series
    8. Mol File: 380381-28-2.mol
  • Chemical Properties

    1. Melting Point: 70-73
    2. Boiling Point: 327.568 °C at 760 mmHg
    3. Flash Point: 151.908 °C
    4. Appearance: /
    5. Density: 1.844 g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.604
    8. Storage Temp.: Keep Cold
    9. Solubility: N/A
    10. PKA: -0.21±0.10(Predicted)
    11. CAS DataBase Reference: Methyl 4-iodopyridine-2-carboxylate(CAS DataBase Reference)
    12. NIST Chemistry Reference: Methyl 4-iodopyridine-2-carboxylate(380381-28-2)
    13. EPA Substance Registry System: Methyl 4-iodopyridine-2-carboxylate(380381-28-2)
  • Safety Data

    1. Hazard Codes: Xi
    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: 380381-28-2(Hazardous Substances Data)

380381-28-2 Usage

Uses

Used in Chemical Research and Industrial Processes:
Methyl 4-iodopyridine-2-carboxylate serves as a reagent in various chemical reactions, facilitating the synthesis of a range of compounds. Its unique structure, including the iodine atom and methyl group, contributes to its reactivity and versatility in organic synthesis.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, Methyl 4-iodopyridine-2-carboxylate is employed as an intermediate in the development of new drugs. Its ability to form various chemical bonds and its halogenated nature make it a valuable component in the synthesis of pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Industry:
Methyl 4-iodopyridine-2-carboxylate also finds application in the agrochemical industry, where it is used as an intermediate in the synthesis of pesticides and other agrochemical products. Its chemical properties allow for the creation of compounds that can effectively control pests and diseases in agriculture.
Used in Dye and Pigment Industry:
In the dye and pigment industry, Methyl 4-iodopyridine-2-carboxylate is utilized as an intermediate for the production of various dyes and pigments. Its unique chemical structure enables the development of colorants with specific properties, such as lightfastness and stability, suitable for various applications, including textiles, plastics, and printing inks.
Used in Material Science:
Methyl 4-iodopyridine-2-carboxylate contributes to the field of material science, where it is employed as a component in the synthesis of advanced materials with specific properties. Its incorporation into polymers and other materials can enhance their performance, such as conductivity, stability, or reactivity, depending on the desired application.

Check Digit Verification of cas no

The CAS Registry Mumber 380381-28-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,0,3,8 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 380381-28:
(8*3)+(7*8)+(6*0)+(5*3)+(4*8)+(3*1)+(2*2)+(1*8)=142
142 % 10 = 2
So 380381-28-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H6INO2/c1-11-7(10)6-4-5(8)2-3-9-6/h2-4H,1H3

380381-28-2SDS

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 Methyl 4-iodopicolinate

1.2 Other means of identification

Product number -
Other names Methyl 4-iodopyridine-2-carboxylate

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:380381-28-2 SDS

380381-28-2Downstream Products

380381-28-2Relevant articles and documents

Allosteric modulators of 5-hydroxytryptamine 2C receptor (5-HT2CR)

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, (2017/01/26)

The disclosure is directed to compounds identified as allosteric modulators of 5-HT 2CR, as well as pharmaceutical compositions and methods using the same. Certain embodiments also include methods of identifying and methods of synthesizing the compounds. Optimization and development of allosteric 5-HT 2CR modulators that bind sites other than the primary ligand binding site generate novel, highly selective, and potent ligands of 5-HT2CR. Such molecules can be used as small molecule probes for the nervous system and as effective therapeutics for a variety of diseases.

ALLOSTERIC MODULATORS OF 5-HYDROXYTRYPTAMINE 2C RECEPTOR (5-HT2CR)

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, (2013/06/27)

[000166] Embodiments of the invention are directed to methods of identifying, methods of synthesizing, and compositions identified as allosteric modulators of 5-HT2cR.

LINCOMYCIN DERIVATIVES POSSESSING ANTIBACTERIAL ACTIVITY

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Page 58-59, (2010/02/06)

Novel lincomycin derivatives are disclosed. These lincomycin derivatives exhibit antibacterial activity. As the compounds of the subject invention exhibit potent activities against bacteria, including gram positive organisms, they are useful antimicrobial agents. Methods of synthesis and of use of the compounds are also disclosed.

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