41486-97-9 Usage
Uses
Used in Pharmaceutical Industry:
Z-VAL-ILE-OH is used as a building block for the synthesis of drugs and other compounds, leveraging its unique combination of essential amino acids and a carboxylic acid group. This allows for the creation of novel pharmaceuticals that can target specific biological pathways or conditions.
Used in Research and Development:
Z-VAL-ILE-OH serves as a valuable compound in scientific research, where its biological and chemical properties can be explored and harnessed for various applications. This may include studying its interactions with biological systems, understanding its role in protein synthesis, and developing new methodologies for its synthesis and modification.
Used in Nutritional Supplements:
Given that valine and isoleucine are essential amino acids, Z-VAL-ILE-OH may be utilized in the development of nutritional supplements designed to support muscle growth, recovery, and overall health. Its inclusion in such supplements could provide a concentrated source of these critical amino acids for individuals seeking to enhance their dietary intake.
Used in Cosmetics and Personal Care Products:
The properties of Z-VAL-ILE-OH, including its role in protein synthesis and its potential for interaction with biological systems, may also find applications in the cosmetics and personal care industry. It could be incorporated into formulations to support skin health, hair growth, or other beauty and wellness applications.
Check Digit Verification of cas no
The CAS Registry Mumber 41486-97-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,8 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 41486-97:
(7*4)+(6*1)+(5*4)+(4*8)+(3*6)+(2*9)+(1*7)=129
129 % 10 = 9
So 41486-97-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H28N2O5/c1-5-13(4)16(18(23)24)20-17(22)15(12(2)3)21-19(25)26-11-14-9-7-6-8-10-14/h6-10,12-13,15-16H,5,11H2,1-4H3,(H,20,22)(H,21,25)(H,23,24)
41486-97-9Relevant articles and documents
An Effective Water-Free Aprotic System for Dissolving Free Amino Acids
Raydnov, M. G.,Klimenko, L. V.,Mitin, Yu. V.
, p. 283 - 287 (2007/10/03)
An effective water-free system was proposed for dissolution and subsequent use in peptide synthesis of free amino acids and their derivatives. It consists of dimethylformamide, a tertiary base, and inorganic additives. Neutral salts (CF3COONa, Ba(ClO4)2, Ca(ClO4)2, NaClO4, BaI2, or Ca(NO3)2) serve as the inorganic additives that increase the solubility of free amino acids in dimethylformamide and provide true 0.2-3 M amino acid solutions. Triethylamine and N-methylmorpholine are most suitable as the tertiary bases. This system was used in reactions with acylating agents: Boc2O, ZOSu, FmocOSu, and activated derivatives of Nα-protected amino acids or peptides. The corresponding amino acid derivatives or Nα-protected di-, tri-, and tetrapeptides were obtained in yields of 80-99 percent at the reaction times of 30-240 min.
