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Methyl 5-chloro-3-fluoropyridine-2-carboxylate is a pyridine derivative with the molecular formula C7H5ClFNO2, featuring a methyl ester group attached to the carboxylate. It is a versatile chemical compound used as an intermediate in the synthesis of biologically active compounds and agricultural chemicals.

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  • 1200498-40-3 Structure
  • Basic information

    1. Product Name: Methyl 5-chloro-3-fluoropyridine-2-carboxylate
    2. Synonyms: Methyl 5-chloro-3-fluoropyridine-2-carboxylate;Methyl 5-chloro-3-fluoropicolinate;Methyl 5-chloro-3-fluoropicolinate, 5-Chloro-3-fluoro-2-(methoxycarbonyl)pyridine;5-Chloro-3-fluoro-pyridine-2-carboxylic acid methyl ester
    3. CAS NO:1200498-40-3
    4. Molecular Formula: C7H5ClFNO2
    5. Molecular Weight: 189.5715032
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1200498-40-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Methyl 5-chloro-3-fluoropyridine-2-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methyl 5-chloro-3-fluoropyridine-2-carboxylate(1200498-40-3)
    11. EPA Substance Registry System: Methyl 5-chloro-3-fluoropyridine-2-carboxylate(1200498-40-3)
  • 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: 1200498-40-3(Hazardous Substances Data)

1200498-40-3 Usage

Uses

Used in Pharmaceutical Industry:
Methyl 5-chloro-3-fluoropyridine-2-carboxylate is used as a key intermediate for the synthesis of various drugs and pharmaceuticals. Its unique structure and functional groups make it a valuable building block in the development of new medications with improved therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, Methyl 5-chloro-3-fluoropyridine-2-carboxylate serves as an essential intermediate for the production of agricultural chemicals, including pesticides and herbicides. Its incorporation into these compounds enhances their effectiveness in controlling pests and weeds, thereby contributing to increased crop yields and food security.
Used in Research and Development:
Methyl 5-chloro-3-fluoropyridine-2-carboxylate is also utilized in the research and development of novel molecules for a wide range of applications. Its unique chemical properties and potential for modification make it an attractive candidate for the creation of new compounds with diverse functionalities and applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1200498-40-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,0,4,9 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1200498-40:
(9*1)+(8*2)+(7*0)+(6*0)+(5*4)+(4*9)+(3*8)+(2*4)+(1*0)=113
113 % 10 = 3
So 1200498-40-3 is a valid CAS Registry Number.

1200498-40-3SDS

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 methyl 5-chloro-3-fluoropyridine-2-carboxylate

1.2 Other means of identification

Product number -
Other names Methyl 5-chloro-3-fluoropicolinate

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:1200498-40-3 SDS

1200498-40-3Relevant articles and documents

NOVEL GALACTOSIDE INHIBITOR OF GALECTINS

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Page/Page column 99; 100, (2019/08/20)

The present invention relates to a compound of the general formula (I) wherein the pyranose ring is a-D-galactopyranose, R1 is selected from the group consisting of (II) wherein the asterix 1 * indicates the carbon atom of the heteroaromatic ring that is covalently attached to the triazole group of formula (I). The compound of formula (I) is suitable for use in a method for treating a disorder relating to the binding of a galectin, such as galectin-1 to a ligand in a mammal, such as a human.

TRICYCLIC PIPERIDINE COMPOUNDS

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Page/Page column 76, (2016/11/21)

The present invention relates to compounds of the formula (I) wherein R1a, R1b, R2, R3, (R4)n and ring (A) are as described in the description, to their preparation, to pharmaceutically acc

TRICYCLIC PIPERIDINE COMPOUNDS

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Page/Page column 119, (2015/06/08)

The present invention relates to compounds of the formula (I), wherein R, R1a, R1b, R2, R3, and X are as described in the description, to their preparation, to pharmaceutically acceptable salts thereof, and to their use as pharmaceuticals, to pharmaceutical compositions containing one or more compounds of formula (I), to methods for the preparation of such compounds of formula (I), and especially to their use as TPH modulators.

TRICYCLIC IMIDAZOLE COMPOUNDS AS INHIBITORS OF TRYPTOPHAN HYDROXYLASE

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Page/Page column 84; 85, (2015/06/08)

The present invention relates to compounds of the formula (I), wherein R1a, R1b, R2, R3, and X are as described in the description, to their preparation, to pharmaceutically acceptable salts thereof, and to thei

SULFUR-CONTAINING HETEROCYCLIC DERIVATIVE HAVING ?-SECRETASE-INHIBITING ACTIVITY

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, (2011/04/25)

The following compound is provided as an agent for treating a disease induced by production, secretion and/or deposition of amyloid β protein, for example,. a compound represented by the formula (I): wherein ruing A is an optionally substituted carbocyclic group or an optionally substituted heterocyclic group, R1 is optionally substituted lower alkyl or the like, R2a and R2b are each independently hydrogen, optionally substituted lower alkyl or the like, R3a and R3c are each independently hydrogen, halogen, hydroxy, optionally substituted lower alkyl or the like, or a pharmaceutically acceptable salt thereof, or a solvate thereof.

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