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2-FLUORO-4-METHOXYBENZOIC ACID ETHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

773135-34-5

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773135-34-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 773135-34-5 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 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 773135-34:
(8*7)+(7*7)+(6*3)+(5*1)+(4*3)+(3*5)+(2*3)+(1*4)=165
165 % 10 = 5
So 773135-34-5 is a valid CAS Registry Number.

773135-34-5SDS

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-fluoro-4-methoxy-benzoate

1.2 Other means of identification

Product number -
Other names ethyl 2-fluoro-4-methoxybenzoate

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:773135-34-5 SDS

773135-34-5Relevant academic research and scientific papers

Synthesis, characterization and biological activity of some new 1,3,4-oxadiazole bearing 2-flouro-4-methoxy phenyl moiety

Chandrakantha,Shetty, Prakash,Nambiyar, Vijesh,Isloor, Nishitha,Isloor, Arun M.

experimental part, p. 1206 - 1210 (2010/04/26)

In the present study a series of new 1,3,4-oxadiazole derivatives containing 2-fluoro-4-methoxy moiety were synthesized. These newly synthesized compounds were characterized by NMR, mass spectral, IR spectral study and also by C, H, N analyses. All the newly synthesized compounds were screened for their antibacterial and antifungal studies. Antimicrobial studies revealed that compounds 4a and 4b showed significant antibacterial activity against Escherichia coli and Pseudomonas aeruginosa Compound 4i showed significant antifungal activity against C. albicans.

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