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Benzoic acid, 2,4,5-trifluoro-, ethyl ester is a colorless, aromatic liquid with a fruity odor and the molecular formula C9H7F3O2. It is a chemical compound commonly used in the production of pharmaceuticals, fragrances, and flavorings due to its antimicrobial properties and versatile applications in various industries.

351354-41-1

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351354-41-1 Usage

Uses

Used in Pharmaceutical Industry:
Benzoic acid, 2,4,5-trifluoro-, ethyl ester is used as an antimicrobial agent for its effectiveness in inhibiting the growth of various bacteria and fungi, ensuring the safety and stability of pharmaceutical products.
Used in Fragrance and Flavoring Industry:
Benzoic acid, 2,4,5-trifluoro-, ethyl ester is used as a key ingredient in the creation of fragrances and flavorings, providing a fruity scent and taste to various products.
Used in Coatings and Adhesives Industry:
Benzoic acid, 2,4,5-trifluoro-, ethyl ester is used as a solvent in the manufacturing of lacquers, varnishes, and resins, contributing to the performance and quality of these materials.
Used in Agricultural Chemicals Industry:
Benzoic acid, 2,4,5-trifluoro-, ethyl ester is utilized in the production of agricultural chemicals, where its antimicrobial properties can help protect crops and enhance their growth.
Used in Organic Synthesis:
Benzoic acid, 2,4,5-trifluoro-, ethyl ester serves as an intermediate in organic synthesis, enabling the creation of various chemical compounds for different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 351354-41-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,1,3,5 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 351354-41:
(8*3)+(7*5)+(6*1)+(5*3)+(4*5)+(3*4)+(2*4)+(1*1)=121
121 % 10 = 1
So 351354-41-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H7F3O2/c1-2-14-9(13)5-3-7(11)8(12)4-6(5)10/h3-4H,2H2,1H3

351354-41-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 2,4,5-trifluorobenzoate

1.2 Other means of identification

Product number -
Other names PC7793

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:351354-41-1 SDS

351354-41-1Downstream Products

351354-41-1Relevant articles and documents

HETEROCYCLIC INHIBITORS OF THE SODIUM CHANNEL

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Page/Page column 65-66, (2015/09/28)

The invention relates to compounds useful in treating conditions associated with voltage-gated ion channel function, particularly conditions associated with sodium channel activity. More specifically, the invention concerns heterocyclic compounds (e.g., compounds according to any of Formulas (l)-(ll l) or Compounds (1 )-(65) of Table 1 ) that are that are useful in treatment of conditions such as epilepsy, cancer, pain, migraine, Parkinson's Disease, mood disorders, schizophrenia, psychosis, tinnitus, amyotropic lateral sclerosis, glaucoma, ischaemia, spasticity disorders, obsessive compulsive disorder, restless leg syndrome and Tourette syndrome.

Pyridonecarboxylic acids as antibacterial agents. VIII. Synthesis and structure-activity relationship of 7-(1-aminocyclopropyl)-4-oxo-1,8-naphthyridine-3-carboxylic acids and 7-(1-aminocyclopropyl)-4-oxoquinoline-3-carboxylic acids

Todo,Nitta,Miyajima,Fukuoka,Yamashiro,Nishida,Saikawa,Narita

, p. 2063 - 2070 (2007/10/02)

4-Oxo-1,8-naphthyridine- and 4-oxoquinoline-3-carboxylic acids (2a, b and 3a-l) possessing a 1-aminocyclopropyl group at the 7-position have been synthesized and evaluated for in vitro antibacterial activities. The three quinolones (3d, h, i) exhibited potent antibacterial activities against both gram-positive and gram-negative bacteria, which are comparable to those of ciprofloxacin (CPFX) and ofloxacin (OFLX). Among the three compounds, the best pharmacological and pharmacokinetic profile was obtained with 3i, an OFLX analogue, which was considerably less toxic than three reference quinolones (1, CPFX, and OFLX).

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