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Ethyl 2-chloro-6-fluoro-benzoat, a chemical compound with the molecular formula C9H8ClFO2, belongs to the benzoate family. It is a colorless liquid with a slightly sweet odor and is stable under normal conditions. ethyl 2-chloro-6-fluoro-benzoat is commonly used in the pharmaceutical and agrochemical industries for the synthesis of various compounds.

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  • 773134-56-8 Structure
  • Basic information

    1. Product Name: ethyl 2-chloro-6-fluoro-benzoat
    2. Synonyms: ethyl 2-chloro-6-fluoro-benzoat;Ethyl 2-chloro-6-fluorobenzoate
    3. CAS NO:773134-56-8
    4. Molecular Formula: C9H8ClFO2
    5. Molecular Weight: 202.6100232
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 773134-56-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 252.1±25.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.266±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: ethyl 2-chloro-6-fluoro-benzoat(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-chloro-6-fluoro-benzoat(773134-56-8)
    11. EPA Substance Registry System: ethyl 2-chloro-6-fluoro-benzoat(773134-56-8)
  • 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: 773134-56-8(Hazardous Substances Data)

773134-56-8 Usage

Uses

Used in Pharmaceutical Industry:
Ethyl 2-chloro-6-fluoro-benzoat is used as an intermediate in the production of various pharmaceuticals. It plays a crucial role in the synthesis of drugs, contributing to the development of new medications and improving the efficacy of existing ones.
Used in Agrochemical Industry:
In the agrochemical industry, ethyl 2-chloro-6-fluoro-benzoat is utilized as an intermediate for the synthesis of various agrochemicals. It helps in the development of pesticides, herbicides, and other agricultural chemicals, enhancing crop protection and yield.
Safety Precautions:
It is essential to handle ethyl 2-chloro-6-fluoro-benzoat with care and use appropriate safety measures when working with it. This chemical can be harmful if inhaled, ingested, or comes in contact with skin or eyes. Proper handling and storage are necessary to ensure the safety of individuals and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 773134-56-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,3,1,3 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 773134-56:
(8*7)+(7*7)+(6*3)+(5*1)+(4*3)+(3*4)+(2*5)+(1*6)=168
168 % 10 = 8
So 773134-56-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H8ClFO2/c1-2-13-9(12)8-6(10)4-3-5-7(8)11/h3-5H,2H2,1H3

773134-56-8SDS

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 ethyl 2-chloro-6-fluorobenzoate

1.2 Other means of identification

Product number -
Other names Benzoic acid,2-chloro-6-fluoro-,ethyl ester

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:773134-56-8 SDS

773134-56-8Relevant articles and documents

Regio- and chemoselective C-H chlorination/bromination of electron-deficient arenes by weak coordination and study of relative directing-group abilities

Sun, Xiuyun,Shan, Gang,Sun, Yonghui,Rao, Yu

supporting information, p. 4440 - 4444 (2013/05/22)

It's all relative: A practical and efficient PdII-catalyzed regio- and chemoselective chlorination/bromination has been developed for the facile synthesis of a broad range of aromatic chlorides. The reaction demonstrates excellent reactivity, good functional-group tolerance, and high yields. A preliminary study was conducted to evaluate relative directing-group abilities of various functionalities. Copyright

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