13104-66-0 Usage
Description
D-4-amino-mandelic acid is a chiral chemical compound with the molecular formula C8H9NO3. It is an amino acid derivative that features a mandelic acid backbone with an amino group attached to the fourth carbon. This unique structure makes it a valuable chiral building block in various industries.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 13104-66-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,0 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13104-66:
(7*1)+(6*3)+(5*1)+(4*0)+(3*4)+(2*6)+(1*6)=60
60 % 10 = 0
So 13104-66-0 is a valid CAS Registry Number.
13104-66-0Relevant articles and documents
7-α-Amino-substituted acylamino-3-(1-carboxymethyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acids
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, (2008/06/13)
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-(tetrazolo-[4,5-b]pyridazin-6-ylthiomethyl)-3-cephem-4-carboxylic acids
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, (2008/06/13)
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.
