126771-41-3

Usage

Uses

Used in Pharmaceutical Industry:
4-(Bromomethyl)phenoxyacetic acid is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
4-(Bromomethyl)phenoxyacetic acid is used as a key component in the preparation of pesticides and herbicides, leveraging its ability to inhibit the growth and development of unwanted plants and pests, thereby enhancing crop protection and yield.
Used in Organic Synthesis:
4-(BROMOMETHYL)PHENOXYACETIC ACID acts as a building block in the synthesis of other organic compounds, serving as a versatile starting material for the creation of a wide range of chemical products across various industries.
Safety Considerations:
It is crucial to handle 4-(Bromomethyl)phenoxyacetic acid with care due to its toxic nature and potential to cause irritation to the skin, eyes, and respiratory system, ensuring proper safety measures are in place during its use and manipulation.

InChI:InChI=1/C9H9BrO3/c10-5-7-1-3-8(4-2-7)13-6-9(11)12/h1-4H,5-6H2,(H,11,12)

Upstream product

• 940-64-7 2-(4-methylphenoxy)acetic acid 

Downstream Products

• 126771-40-2 2,4-dichlorophenyl-4-bromomethyl-phenoxyacetate 
• 68858-21-9 [4-(hydroxymethyl)phenoxy]acetic acid 
• 1404550-02-2 1,3-bis(4-(carboxymethoxy)benzyl)-4,5-dichloro-1H-imidazol-3-ium bromide 
• 1404550-00-0 1-(4-(carboxymethoxy)benzyl)-4,5-dichloro-3-(naphthalen-2-ylmethyl)-1H-imidazol-3-ium bromide 
• 126771-53-7 (R)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-tritylsulfanyl-propionic acid 4-(2,4-dichloro-phenoxycarbonylmethoxy)-benzyl ester 
• 126771-47-9 (S)-6-tert-Butoxycarbonylamino-2-(9H-fluoren-9-ylmethoxycarbonylamino)-hexanoic acid 4-(2,4-dichloro-phenoxycarbonylmethoxy)-benzyl ester 
• 126771-52-6 (S)-3-(4-tert-Butoxy-phenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-propionic acid 4-(2,4-dichloro-phenoxycarbonylmethoxy)-benzyl ester 
• 126771-44-6 (S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-pentanedioic acid 5-tert-butyl ester 1-[4-(2,4-dichloro-phenoxycarbonylmethoxy)-benzyl] ester 
• 126771-48-0 (S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-(1H-indol-3-yl)-propionic acid 4-(2,4-dichloro-phenoxycarbonylmethoxy)-benzyl ester 
• 126771-45-7 (S)-3-tert-Butoxy-2-(9H-fluoren-9-ylmethoxycarbonylamino)-propionic acid 4-(2,4-dichloro-phenoxycarbonylmethoxy)-benzyl ester 
• 126771-50-4 (S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-3-phenyl-propionic acid 4-(2,4-dichloro-phenoxycarbonylmethoxy)-benzyl ester 
• 126771-42-4 (S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-succinamic acid 4-(2,4-dichloro-phenoxycarbonylmethoxy)-benzyl ester 
• 126771-49-1 (S)-Pyrrolidine-1,2-dicarboxylic acid 2-[4-(2,4-dichloro-phenoxycarbonylmethoxy)-benzyl] ester 1-(9H-fluoren-9-ylmethyl) ester 
• 126771-51-5 (S)-2-(9H-Fluoren-9-ylmethoxycarbonylamino)-4-methyl-pentanoic acid 4-(2,4-dichloro-phenoxycarbonylmethoxy)-benzyl ester 

Relevant academic research and scientific papers

Racemization free attachment of amino acids to a solid phase

This invention pertains to amino acids attached to a solid support in a racemization free manner and to a method of covalently linking amino acids to solid supports for use in solid phase peptide syntheses.

AN EFFICIENT METHOD FOR RACEMIZATION FREE ATTACHMENT OF 9-FLUORENYLMETHYLOXYCARBONYL-AMINO ACIDS TO PEPTIDE SYNTHESIS SUPPORTS

An efficient, general, and racemization free method of covalently attaching N α-Fmoc protected amino acids to solid supports for peptide synthesis is described.The process involves the preparation of 2,4-dichlorophenyl-N α-Fmoc- aminoacyl-4-oxymethyl-phen