Welcome to LookChem.com Sign In|Join Free
  • or
(3S)-3-AMINO-3-(2,4-DIMETHOXYPHENYL)PROPANOIC ACID is a chemical compound that belongs to the class of amino acids. It is a derivative of proline, an essential amino acid that plays a crucial role in protein synthesis and overall cellular function. The presence of the amino group and the dimethoxyphenyl group makes (3S)-3-AMINO-3-(2,4-DIMETHOXYPHENYL)PROPANOIC ACID important in the field of medicinal chemistry, as it can potentially be used as a building block for the synthesis of various pharmaceuticals and biologically active molecules. Its specific chemical structure and properties make it a valuable tool for researchers in drug discovery and development.

951174-49-5

Post Buying Request

951174-49-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

951174-49-5 Usage

Uses

Used in Pharmaceutical Industry:
(3S)-3-AMINO-3-(2,4-DIMETHOXYPHENYL)PROPANOIC ACID is used as a building block for the synthesis of various pharmaceuticals and biologically active molecules. Its unique chemical structure and properties make it a valuable tool for researchers in drug discovery and development.
Used in Medicinal Chemistry:
(3S)-3-AMINO-3-(2,4-DIMETHOXYPHENYL)PROPANOIC ACID is used as a key component in the development of new drugs and therapeutic agents. Its presence in the class of amino acids and its derivative nature from proline make it a promising candidate for the creation of novel pharmaceuticals with potential therapeutic benefits.

Check Digit Verification of cas no

The CAS Registry Mumber 951174-49-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,1,1,7 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 951174-49:
(8*9)+(7*5)+(6*1)+(5*1)+(4*7)+(3*4)+(2*4)+(1*9)=175
175 % 10 = 5
So 951174-49-5 is a valid CAS Registry Number.

951174-49-5Relevant academic research and scientific papers

Parallel synthesis of homochiral β-amino acids

Davies, Stephen G.,Mulvaney, Andrew W.,Russell, Angela J.,Smith, Andrew D.

, p. 1554 - 1566 (2008/02/09)

The parallel asymmetric synthesis of an array of 30 β-amino acids of high enantiomeric purity using the conjugate addition of homochiral lithium N-benzyl-N-(α-methylbenzyl)amide as the key step is accomplished. The experimental simplicity and highly practical nature of the protocol is demonstrated by the efficient parallel conversion of 15 α,β-unsaturated esters to both enantiomeric series of the corresponding β-amino acids in high overall yields and selectivities with minimal purification involved in each step of the reaction protocol.

One-Pot Cyclization of Alkoxy-3-Aminoindan-1-ones.

Dallemagne, Patrick,Rault, Sylvain,Pilo, Juan Carlos,Foloppe, Marie Paule,Robba, Max

, p. 6327 - 6328 (2007/10/02)

3-Amino-3-alkoxyphenylpropionic acids, prepared from alkoxybenzaldehydes, are cyclized in one step into 3-aminoindan-1-ones using trifluoroacetic acid and trifluoroacetic anhydride. Key Words: One-pot cyclization; Aminoindanones; Electrodonating substitue

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 951174-49-5