225233-69-2 Usage
Uses
Used in Pharmaceutical Industry:
2-Methyl-DL-homophenylalanine is used as a pharmaceutical intermediate for the synthesis of various drugs and therapeutic agents. Its unique structure allows it to be incorporated into the development of new medications, potentially offering novel treatments for a range of diseases and conditions.
Used in Peptide and Protein Synthesis:
In the field of biochemistry, 2-Methyl-DL-homophenylalanine is utilized as a building block in the synthesis of custom peptides and proteins. Its incorporation into these biological molecules can alter their properties, enabling the creation of new compounds with specific functions or improved stability.
Used in Food Industry:
2-Methyl-DL-homophenylalanine is used as a food additive, where it may contribute to the enhancement of flavor, texture, or other qualities in food products. Its role in this industry is based on its chemical properties and potential effects on the sensory attributes of food.
Used in Animal Feed Supplementation:
In the agricultural sector, 2-Methyl-DL-homophenylalanine may be employed as a supplement in animal feed. Its inclusion can support the nutritional needs of livestock, potentially improving their health and growth performance.
Overall, 2-Methyl-DL-homophenylalanine is a versatile chemical with a range of applications across different industries, highlighting its importance in both pharmaceutical development and food production.
Check Digit Verification of cas no
The CAS Registry Mumber 225233-69-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,5,2,3 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 225233-69:
(8*2)+(7*2)+(6*5)+(5*2)+(4*3)+(3*3)+(2*6)+(1*9)=112
112 % 10 = 2
So 225233-69-2 is a valid CAS Registry Number.
225233-69-2Relevant academic research and scientific papers
Synthesis of optically active (2-arylvinyl)glycine derivatives by palladium-catalyzed arylation of (s)-n-(benzyloxycarbonyl)vinylglycine
Itaya, Taisuke,Hozumi, Yoshitaka
, p. 1094 - 1101 (2007/10/03)
Phenyl, tolyl, anisyl, and 1-naphthyl iodides (7a-g,n) smoothly reacted with (S)-N-(benzyloxycarbonyl)-vinylglycine (6) in H2O in the presence of Pd(OAc)2, Bu4NCI, and NaHCO3 at 45°C, producing [S-(E)]-(2- arylvinyl)glycine derivatives 8a-g, n of high enantiomeric purity. The yields of the reactions of 3- (7f), 2- (7e), and 4-iodoanisoles (7g) increased in this order. This relationship between the yield and the position of substitution has been found to hold for bromophenyl iodides (7i-k), although somewhat lower chemical and optical yields were realized in these cases. Phenyl iodide 71 carrying an electron-withdrawing 4-acetyl group gave an unsatisfactory result, and more electron-deficient 4-nitrophenyl iodide (7m) did not provide the desired product. All these results suggest that the reaction is advantageous with electron-sufficient substrates 7. However, this was not the case for 4-iodophenol (7h), as well as some heterocyclic iodides.
