1810074-59-9 Usage
Description
(R)-5-Amino-5-phenylpentanoic acid hydrochloride is a chemical compound derived from the amino acid valine, featuring an added phenyl group. With the molecular formula C11H15NO2Cl, this hydrochloride salt form is widely utilized in the pharmaceutical and research sectors as a chiral building block and intermediate for synthesizing a variety of compounds.
Uses
Used in Pharmaceutical Industry:
(R)-5-Amino-5-phenylpentanoic acid hydrochloride is used as a chiral building block for the development of neuroprotective agents and drugs targeting neurological disorders. Its unique structure allows for the creation of compounds that can potentially protect and repair neurons, offering new treatment options for patients suffering from such conditions.
Used in Research and Development:
In the research and development sector, (R)-5-Amino-5-phenylpentanoic acid hydrochloride serves as a key intermediate in the synthesis of drugs aimed at treating depression, anxiety, and other mood disorders. Its role in the development of these medications is crucial, as it can contribute to the creation of more effective and targeted therapies for individuals struggling with these mental health issues.
Used in Peptide and Bioactive Compound Production:
Furthermore, (R)-5-Amino-5-phenylpentanoic acid hydrochloride is employed in the production of various peptides and other bioactive compounds. Its versatile structure makes it a valuable component in the synthesis of molecules with potential applications in medicine, biotechnology, and other related fields.
Check Digit Verification of cas no
The CAS Registry Mumber 1810074-59-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,8,1,0,0,7 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1810074-59:
(9*1)+(8*8)+(7*1)+(6*0)+(5*0)+(4*7)+(3*4)+(2*5)+(1*9)=139
139 % 10 = 9
So 1810074-59-9 is a valid CAS Registry Number.
1810074-59-9Relevant articles and documents
An Efficient Two-Step Preparation of α-, β-, γ- or δ-Amino Acids from 2-Pyrazinones, 2-Hydroxypyrimidines or 2-Pyridones Respectively
Zacharie, Boulos,Abbott, Shaun D.,Baigent, Christopher B.,Doyle, Christopher,Yalagala, Ravi Shekar
, p. 6486 - 6493 (2018)
A practical and efficient two-step procedure is reported for the preparation of a variety of α-, β-, γ- and δ-amino acids from 2-pyridone, 2-pyrazinone or 2-hydroxypyrimidine and derivatives. The procedure is amenable to scale-up and in most cases no chromatographic purification of the product is required. This approach is useful, especially in the synthesis of amino acids or deuterated amino acids that are not obtained by other methods.
