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2-Fluoro-4-(trifluoromethyl)benzaldehyde is an organic compound characterized by the presence of a fluorine atom at the 2nd position and a trifluoromethyl group at the 4th position on a benzene ring. It is an aldehyde, which means it contains a carbonyl group (C=O) bonded to a hydrogen atom and an aromatic ring. 2-FLUORO-4-(TRIFLUOROMETHYL)BENZALDEHYDE is known for its unique chemical properties and potential applications in various fields.

89763-93-9

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89763-93-9 Usage

Uses

Used in Pharmaceutical Industry:
2-Fluoro-4-(trifluoromethyl)benzaldehyde is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity make it a valuable building block for the development of new drugs with improved therapeutic properties.
Used in Chemical Synthesis:
In the field of organic chemistry, 2-Fluoro-4-(trifluoromethyl)benzaldehyde is used as a versatile starting material for the synthesis of a wide range of organic compounds. Its reactivity allows for various chemical reactions, such as condensation, reduction, and substitution, enabling the formation of diverse chemical entities.
Used in the Synthesis of Methyl 3-amino-6-(trifluoromethyl)benzo[b]thiophene-2-carboxylate:
2-Fluoro-4-(trifluoromethyl)benzaldehyde is specifically used in the synthesis of methyl 3-amino-6-(trifluoromethyl)benzo[b]thiophene-2-carboxylate, a compound with potential applications in various industries. This synthesis showcases the compound's utility in creating complex and functionalized molecules for further use.

Check Digit Verification of cas no

The CAS Registry Mumber 89763-93-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,6 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 89763-93:
(7*8)+(6*9)+(5*7)+(4*6)+(3*3)+(2*9)+(1*3)=199
199 % 10 = 9
So 89763-93-9 is a valid CAS Registry Number.
InChI:InChI=1/C20H17F17O6/c1-3-41-9(38)7-12(10(39)42-4-2)5-8(43-11(12)40)6-13(21,22)14(23,24)15(25,26)16(27,28)17(29,30)18(31,32)19(33,34)20(35,36)37/h8H,3-7H2,1-2H3

89763-93-9 Well-known Company Product Price

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  • Alfa Aesar

  • (A18500)  2-Fluoro-4-(trifluoromethyl)benzaldehyde, 97%   

  • 89763-93-9

  • 1g

  • 362.0CNY

  • Detail
  • Alfa Aesar

  • (A18500)  2-Fluoro-4-(trifluoromethyl)benzaldehyde, 97%   

  • 89763-93-9

  • 5g

  • 1292.0CNY

  • Detail
  • Alfa Aesar

  • (A18500)  2-Fluoro-4-(trifluoromethyl)benzaldehyde, 97%   

  • 89763-93-9

  • 25g

  • 5075.0CNY

  • Detail

89763-93-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Fluoro-4-(trifluoromethyl)benzaldehyde

1.2 Other means of identification

Product number -
Other names 2-FLUORO-4-(TRIFLUOROMETHYL)BENZALDEHYDE

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:89763-93-9 SDS

89763-93-9Relevant academic research and scientific papers

Elemental fluorine. Part 21. (1) direct fluorination of benzaldehyde derivatives

Chambers, Richard D.,Sandford, Graham,Trmcic, Jelena,Okazoe, Takashi

, p. 339 - 344 (2013/01/03)

Direct fluorination of a range of benzaldehyde derivatives gives mixtures of fluorobenzaldehyde and benzoyl fluoride products in ratios that depend upon the nature of the ring substituent Electron-withdrawing substituents give predominantly benzoyl fluoride derivatives, whereas electron-donating substituents lead to fluoroarene systems. Separation of ring-fluorinated products can be easily accomplished by esterification of the benzoyl fluoride side products. Scale-up of these processes to provide significant quantities of appropriate fluorobenzaldehyde systems has also been achieved using continuous flow techniques.

Vanilloid receptor ligands and their use in treatments

-

, (2008/06/13)

Compounds having the general structure and compositions containing them, for the treatment of acute, inflammatory and neuropathic pain, dental pain, general headache, migraine, cluster headache, mixed-vascular and non-vascular syndromes, tension headache, general inflammation, arthritis, rheumatic diseases, osteoarthritis, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorders, psoriasis, skin complaints with inflammatory components, chronic inflammatory conditions, inflammatory pain and associated hyperalgesia and allodynia, neuropathic pain and associated hyperalgesia and allodynia, diabetic neuropathy pain, causalgia, sympathetically maintained pain, deafferentation syndromes, asthma, epithelial tissue damage or dysfunction, herpes simplex, disturbances of visceral motility at respiratory, genitourinary, gastrointestinal or vascular regions, wounds, burns, allergic skin reactions, pruritis, vitiligo, general gastrointestinal disorders, gastric ulceration, duodenal ulcers, diarrhea, gastric lesions induced by necrotising agents, hair growth, vasomotor or allergic rhinitis, bronchial disorders or bladder disorders.

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