7765-11-9 Usage
Uses
Used in Scientific Research:
Chloroacetyl-DL-Phenylalanine is used as a research compound for exploring its chemical properties, interactions with biological systems, and potential applications in various scientific fields. Its presence of two enantiomers makes it an interesting subject for studies in biochemistry and pharmacology, as these mirror image molecules can exhibit different biological activities and interactions.
Used in Biochemical Studies:
In the field of biochemistry, Chloroacetyl-DL-Phenylalanine is used as a model compound to investigate the effects of enantiomers on biological processes. This can help researchers understand the role of chirality in molecular recognition and the development of new drugs and therapeutic agents.
Used in Pharmaceutical Development:
Chloroacetyl-DL-Phenylalanine may be used as a starting material or intermediate in the synthesis of new pharmaceutical compounds. Its unique structure and the presence of enantiomers can provide insights into the design of more effective and targeted drugs, potentially leading to the development of novel therapeutic agents.
Used in Analytical Chemistry:
In analytical chemistry, Chloroacetyl-DL-Phenylalanine can be used as a reference compound or standard for the development and validation of analytical methods. Its distinct properties can help in the accurate determination of the enantiomeric composition of other chiral compounds, which is essential in quality control and regulatory compliance.
Used in Materials Science:
The potential applications of Chloroacetyl-DL-Phenylalanine in materials science could involve its use in the development of new materials with unique properties, such as chiral catalysts, sensors, or materials with specific optical or electronic properties. The presence of enantiomers in CHLOROACETYL-DL-PHENYLALANINE may contribute to the creation of novel materials with enhanced performance characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 7765-11-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,6 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7765-11:
(6*7)+(5*7)+(4*6)+(3*5)+(2*1)+(1*1)=119
119 % 10 = 9
So 7765-11-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H12ClNO3/c12-7-10(14)13-9(11(15)16)6-8-4-2-1-3-5-8/h1-5,9H,6-7H2,(H,13,14)(H,15,16)/t9-/m1/s1
7765-11-9Relevant academic research and scientific papers
Kinetic Resolution of Unnatural and Rarely Occuring Amino Acids: Enantioselective Hydrolysis of N-Acyl Amino Acids Catalyzed by Acylase I
Chenault, H. Keith,Dahmer, Juergen,Whitesides, George M.
, p. 6354 - 6364 (2007/10/02)
Acylase I (aminoacylase; N-acylamino-acid amidohydrolase, EC 3.5.1.14, from porcine kidney and the fungus Aspergillus) is broadly applicable enzymatic catalyst for the kinetic resolution of unnatural and rarely occuring α-amino acids.Its enantioselectivity for the hydrolysis of N-acyl L-α-amino acids is nearly absolute, yet it accepts substrates having a wide range of structure and functionality.This paper reports the initial rates of enzyme-catalyzed hydrolysis of over 50 N-acyl amino acids and analogues, the stabilities of the enzymes in aqueous and aqueous/organic solutions, and the effects of different acyl groups and metal ions on the rates of enzymatic hydrolysis.Eleven α-amino and α-methyl α-amino acids were resolved on a 2-29-g scale.Crude L- and D-amino acid products had generally >90percent ee.The utility of resolved amino acids as chiral synthons was illustrated by the preparation of (R)- and (S)-1-butene oxide and the diastereoselective (cis:trans, 7-8:1) iodolactonization of three 2-amino-4-alkenoic acid derivatives.
Halogenated acylamino acids as fungicides
-
, (2008/06/13)
Compounds of the formula STR1 wherein Y is chlorinated alkyl of 1 to 6 carbon atoms; wherein R is Cn H2n or R2 Cn H2n-1 wherein n is an integer of 1 to 11 and R2 is aralkyl or carboxyalky; and wherein R' is hydrogen, alkyl, haloalkyl, alkaryl or aryl; have fungicidal activity. The compounds can be used in the free acid or salt form.
