82006-84-6

Usage

Uses

Used in Chemical Research:
(3E)-2,5-diamino-2-(fluoromethyl)pent-3-enoic acid is used as a research compound for studying its chemical properties and reactivity. Its unique structure allows scientists to explore new reactions and mechanisms that could lead to the development of novel chemical processes.
Used in Pharmaceutical Development:
(3E)-2,5-diamino-2-(fluoromethyl)pent-3-enoic acid is used as a starting material or intermediate in the synthesis of new pharmaceutical compounds. Its potential biological activities and unique structure make it a promising candidate for the development of new drugs, particularly in areas where existing treatments are limited or ineffective.
Used in Drug Design:
(3E)-2,5-diamino-2-(fluoromethyl)pent-3-enoic acid is used as a structural component in drug design, where its fluoromethyl group and double bond may confer specific properties to the resulting drug molecules. This can lead to the creation of new drugs with improved pharmacokinetics, selectivity, and efficacy.
Used in Biochemical Studies:
(3E)-2,5-diamino-2-(fluoromethyl)pent-3-enoic acid is used in biochemical studies to investigate its interactions with biological systems. Understanding how (3E)-2,5-diamino-2-(fluoromethyl)pent-3-enoic acid interacts with enzymes, receptors, or other biomolecules can provide insights into its potential therapeutic applications and mechanisms of action.
Note: The specific applications and industries for (3E)-2,5-diamino-2-(fluoromethyl)pent-3-enoic acid are not explicitly mentioned in the provided materials. The uses listed above are inferred based on the compound's potential properties and typical applications of similar organic compounds in the fields of chemical research and pharmaceutical development.

Upstream product

• 151028-34-1 (E)-5-Bromo-2-tert-butoxycarbonylamino-2-fluoromethyl-pent-3-enoic acid methyl ester 
• 151028-35-2 (E)-2-tert-Butoxycarbonylamino-5-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-2-fluoromethyl-pent-3-enoic acid methyl ester 
• 151028-33-0 2-tert-Butoxycarbonylamino-2-fluoromethyl-3-hydroxy-pent-4-enoic acid methyl ester 

Relevant academic research and scientific papers

A versatile entry into the synthesis of α-(monofluoromethyl) amino acids : Preparation of α-(monofluoromethyl) serine and (E)-dehydro-α-(monofluoromethyl) ornithine

A new entry to the synthesis of α-(monofluoromethyl) amino acids is described. The synthesis is based on a Strecker reaction on an α-(monofluoromethyl) ketone. As an example, α-(monofluoromethyl) serine was synthesized and used as starting material for a new synthesis of (E)-dehydro-α-(monoflouromethyl) ornithine.

Fluorinated pentene diamine derivatives

Fluorinated alkenylene diamine compounds are inhibitors of ornithine decarboxylase enzyme in vivo and have the following formula: STR1 wherein: Ra represents hydrogen or R2, where R2 is as defined below; Rb represents hydrogen or, when Ra is hydrogen, R2, where R2 is as defined below; Rc represents hydrogen or --COR3, where R3 is as defined below; R1 represents hydrogen or C1 --C6 alkyl; each R2, independently, represents C2 -C5 alkylcarbonyl, phenylcarbonyl, phenyl-(C1 -C4 alkyl) carbonyl, or an aminocarboxylic acid residue derived by removal of an hydroxy group from a carboxy moiety of an L-aminocarboxylic acid; R3 represents hydroxy, or, when Ra and Rb are both hydrogen, C1 -C8 alkoxy, --NR4 R5, where R4 and R5 are as defined below, or an aminocarboxylic acid residue derived by removal of an hydrogen atom from the amino moiety of an L-aminocarboxylic acid; R4 and R5, independently, represent hydrogen or C1 -C4 alkyl; and p represents 1 or 2.

Method of inhibiting the growth of protozoa

α-Substituted amines and α-substituted-α-amino acids are described which are useful in inhibiting the growth of protozoa in animals.

Method of inhibiting algae

α-Substituted amines and α-substituted-α-amino acids are described which are useful in controlling the growth of algae.