170242-34-9 Usage
Description
2-AMINO-5-[1,3]DIOXOLAN-2-YL-PENTANOIC ACID is a chemical compound with the molecular formula C9H15NO4. It is a derivative of pentanoic acid and contains a dioxolane ring. This white solid at room temperature is sparingly soluble in water and serves as a building block in organic synthesis and pharmaceutical research. Its unique structure and properties make it a valuable component in the development of potential pharmaceutical drugs and new chemicals for various industrial applications.
Uses
Used in Pharmaceutical Research and Development:
2-AMINO-5-[1,3]DIOXOLAN-2-YL-PENTANOIC ACID is used as a key building block for the synthesis of potential pharmaceutical drugs. Its unique structure allows it to be incorporated into various drug candidates, potentially leading to the discovery of new treatments for a range of medical conditions.
Used in Organic Synthesis:
In the field of organic synthesis, 2-AMINO-5-[1,3]DIOXOLAN-2-YL-PENTANOIC ACID is used as a versatile intermediate. Its dioxolane ring and amino group provide opportunities for further chemical reactions, making it a valuable component in the creation of new chemical entities for a variety of applications.
Used in Industrial Applications:
2-AMINO-5-[1,3]DIOXOLAN-2-YL-PENTANOIC ACID is also utilized in various industrial applications. Its properties make it suitable for use in the development of new chemicals and materials, contributing to advancements in different sectors such as materials science, agriculture, and environmental technology.
Check Digit Verification of cas no
The CAS Registry Mumber 170242-34-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,2,4 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 170242-34:
(8*1)+(7*7)+(6*0)+(5*2)+(4*4)+(3*2)+(2*3)+(1*4)=99
99 % 10 = 9
So 170242-34-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H15NO4/c9-6(8(10)11)2-1-3-7-12-4-5-13-7/h6-7H,1-5,9H2,(H,10,11)
170242-34-9Relevant articles and documents
The combination of hydroformylation and biocatalysis for the large-scale synthesis of (S)-allysine ethylene acetal
Cobley, Christopher J.,Lloyd, Michael C.,Simmonds, Shaun,Hanson, Christopher H.,Peng, Wei Jun
experimental part, p. 284 - 290 (2011/10/02)
The compound, (S)-2-amino-5-[1,3]dioxolan-2-yl-pentanoic acid [(S)-allysine ethylene acetal], is a key intermediate in a number of angiotension-I converting enzyme (ACE) and neutral endopeptidase (NEP) inhibitors currently in clinical trials. Through a co
Method for producing L-Allysine acetal
-
, (2008/06/13)
A method for producing L-allysine acetal represented by general formula (II), comprising reacting D,L-allysinamide acetal represented by general formula (I) with cells of microorganism or treated cell product having an activity of stereoselectively hydrolyzing L-allysinamide acetal, wherein R1and R2, which may be the same or different, each independently represent a lower alkyl group, or R1and R2are combined to form an alkylene group represented by [CH2]n, and n is 2 to 3. D,L-allysinamide acetal represented by general formula (I) is also in the scope of the invention. According to the present invention, L-allysine acetal useful as a raw material for medicine can be produced in a smaller number of steps at low costs.
