13893-43-1 Usage
Description
(R)-2-AMINO-PENTANOIC ACID ETHYL ESTER, also known as ethyl (R)-2-aminopentanoate, is a chemical compound with the molecular formula C7H15NO2. It is a chiral building block that is widely utilized in the pharmaceutical industry for the synthesis of various pharmaceutical products. (R)-2-AMINO-PENTANOIC ACID ETHYL ESTER is known to exhibit biological activity and has been employed as a precursor in the preparation of enantiomerically pure drugs. Furthermore, it has been investigated for its potential applications in organic chemistry and medicinal chemistry research, with a focus on the development of new drugs and other biologically active compounds.
Uses
Used in Pharmaceutical Industry:
(R)-2-AMINO-PENTANOIC ACID ETHYL ESTER is used as a chiral building block for the synthesis of various pharmaceutical products. Its application is due to its ability to contribute to the creation of enantiomerically pure drugs, which are essential for ensuring the desired therapeutic effects and minimizing potential side effects.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, (R)-2-AMINO-PENTANOIC ACID ETHYL ESTER is used as a precursor in the preparation of enantiomerically pure drugs. Its application is based on its chiral nature, which allows for the development of more effective and targeted medications with fewer side effects.
Used in Organic Chemistry Research:
(R)-2-AMINO-PENTANOIC ACID ETHYL ESTER is also utilized in organic chemistry research, where it serves as a valuable compound for the development of new drugs and other biologically active compounds. Its application in this field is due to its unique chemical properties and potential for further modification and functionalization.
Used in Drug Development:
(R)-2-AMINO-PENTANOIC ACID ETHYL ESTER has potential applications in the development of new drugs, as it can be used as a starting material or a key intermediate in the synthesis of novel pharmaceutical compounds. Its application in drug development is driven by its biological activity and the possibility of creating enantiomerically pure drugs with improved therapeutic profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 13893-43-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,9 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13893-43:
(7*1)+(6*3)+(5*8)+(4*9)+(3*3)+(2*4)+(1*3)=121
121 % 10 = 1
So 13893-43-1 is a valid CAS Registry Number.
13893-43-1Relevant articles and documents
Efficient synthesis of α-substituted amino acid ester: Alkylation and hydrogenation removal of Schiff's base protecting group
Ansari, Aslam M.,Ugwu, Sydney O.
, p. 2330 - 2340 (2008)
A general and efficient synthetic route to α-amino acids by alkylation of the sodium salt of Schiff base ester 1 has been described previously. The α-substituted ethyl glycinates 4a-g are prepared in excellent yield by a two-step sequence involving regios
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Hauser,Reynolds
, p. 4250 (1948)
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The use of alpha-amino acids in the synthesis of derivatives of 2-aminoethanethiol as potential antiradiation agents.
Piper,Stringfellow Jr.,Johnston
, p. 911 - 920 (2007/10/05)
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