13104-66-0

Usage

Uses

Used in Pharmaceutical Industry:
D-4-amino-mandelic acid is utilized as a chiral building block for the synthesis of pharmaceuticals. Its unique structure allows for the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical industry, D-4-amino-mandelic acid serves as a chiral building block for the synthesis of agrochemicals. This enables the creation of more effective and targeted pesticides and other agricultural products.
Used in Polymer Production:
D-4-amino-mandelic acid is also used in the production of polymers. Its incorporation into polymer structures can lead to materials with novel properties and applications.
Used as a Precursor in Organic Synthesis:
D-4-amino-mandelic acid acts as a precursor for the synthesis of other organic compounds, expanding its utility in various chemical reactions and product development.
Used in Therapeutic Applications:
D-4-amino-mandelic acid has potential therapeutic applications due to its ability to inhibit the enzyme phenylalanine ammonia lyase. This property could make it useful in the treatment of certain diseases, offering new avenues for medical research and development.

Upstream product

• 10098-39-2 2-hydroxy-2-(4-nitrophenyl)acetic acid 
• 555-16-8 4-nitrobenzaldehdye 

Downstream Products

• 101090-84-0 (4-amino-phenyl)-(toluene-4-sulfonyloxy)-acetic acid 

Relevant academic research and scientific papers

7-α-Amino-substituted acylamino-3-(1-carboxymethyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acids

Certain 7-acylamido-3-(1-carboxy-loweralkyl-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acids and their salts and easily hydrolyzed esters of the 4-carboxyl group were synthesized and found to be potent antibacterial agents which exhibited good aqueous solubility. In a preferred embodiment the 7-substituent was 2'-aminomethylphenylacetamido.

7-(D-α-Hydroxy-2-arylacetamido)-3-(2-carboxyalkyl-2,3-dihydro-s-triazolo-[4,3-b]pyridazin-3-on-6-ylthiomethyl)-3-cephem-4-carboxylic acids and derivatives

7-(D-α-Hydroxy-2-arylacetamido)-3-(2-carboxyalkyl-2,3-dihydro-s-triazolo[4,3-b]pyridazin-3-on-6-ylthiomethyl)-3-cephem-4-carboxylic acids and derivatives containing blocking groups on the α-hydroxy group and their nontoxic, pharmaceutically acceptable salts are valuable as antibacterial agents and are particularly valuable as therapeutic agents in poultry and in animals, including man, in the treatment of infectious diseases caused by many Gram-positive and Gram-negative bacteria. A preferred compound is 7-(D-mandelamido)-3-(2-carboxyalkyl-2,3-dihydro-s-triazolo[4,3-b]pyridazin-3-on-6-ylthiomethyl)-3-cephem-4-carboxylic acid.

7-(D-α-Hydroxy-2-arylacetamido)-3-(tetrazolo-[4,5-b]pyridazin-6-ylthiomethyl)-3-cephem-4-carboxylic acids

7-(D-α-Hydroxy-2-arylacetamido)-3-(tetrazolo-[4,5-b]pyridazin-6-ylthiomethyl)-3-cephem-4-carboxylic acids and their nontoxic, pharmaceutically acceptable salts are valuable as antibacterial agents and are particularly valuable as therapeutic agents in poultry and animals, including man, in the treatment of infectious diseases caused by many Gram-positive and Gram-negative bacteria.