109971-52-0 Usage
Description
(2R)-2-AMINO-2-(3-CHLORO-4-METHOXYPHENYL)ACETIC ACID is a chiral amino acid derivative with a molecular formula C9H11ClNO3. It is composed of a central carbon atom bonded to an amino group, a carboxylic acid group, and a phenyl group substituted with a chlorine atom and a methoxy group. (2R)-2-AMINO-2-(3-CHLORO-4-METHOXYPHENYL)ACETIC ACID is commonly used as a building block in the synthesis of pharmaceutical drugs and can be found in various medications. It is also known for its potential pharmacological activities, including anti-inflammatory and analgesic properties. Additionally, its chiral nature makes it an important component in the development of chiral drugs.
Uses
Used in Pharmaceutical Industry:
(2R)-2-AMINO-2-(3-CHLORO-4-METHOXYPHENYL)ACETIC ACID is used as a building block for the synthesis of pharmaceutical drugs. Its chiral nature allows for the development of chiral drugs, which can have different pharmacological effects and properties compared to their non-chiral counterparts.
Used in Medications:
(2R)-2-AMINO-2-(3-CHLORO-4-METHOXYPHENYL)ACETIC ACID is used as an active ingredient in various medications. Its potential pharmacological activities, such as anti-inflammatory and analgesic properties, contribute to the therapeutic effects of these medications.
Used in Drug Development:
(2R)-2-AMINO-2-(3-CHLORO-4-METHOXYPHENYL)ACETIC ACID is used in the research and development of new drugs. Its unique structure and properties make it a valuable compound for exploring novel therapeutic approaches and creating innovative pharmaceutical products.
Check Digit Verification of cas no
The CAS Registry Mumber 109971-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,9,7 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 109971-52:
(8*1)+(7*0)+(6*9)+(5*9)+(4*7)+(3*1)+(2*5)+(1*2)=150
150 % 10 = 0
So 109971-52-0 is a valid CAS Registry Number.
109971-52-0Relevant articles and documents
Ruthenium-promoted diaryl ether synthesis in the construction of the F- O-G ring system of a teicoplanin model
Pearson, Anthony J.,Belmont, Philippe O.
, p. 1671 - 1675 (2007/10/03)
An end-game approach is described for the synthesis of glycopeptide antibiotics related to teicoplanin, using ruthenium-promoted diaryl ether formation, followed by cycloamidation. (C) 2000 Elsevier Science Ltd.
