38075-43-3 Usage
Description
(2S)-2-[(Z)-[(5-chloro-2-hydroxy-phenyl)-phenyl-methylene]amino]-3-methyl-butanoic acid is a complex and potentially biologically active derivative of the amino acid leucine. It features a unique structural arrangement, including a hydroxyphenyl group, a phenyl group, a chloro substituent, a methylene bridge, and an amino group, all attached to a central carbon atom. The presence of a methyl and carboxylic acid functional group further contributes to its chemical diversity. The specific (2S) and (Z) stereochemistry of the molecule suggests that its interactions with biological systems may be influenced by its spatial configuration, indicating a wide range of potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
(2S)-2-[(Z)-[(5-chloro-2-hydroxy-phenyl)-phenyl-methylene]amino]-3-methyl-butanoic acid is used as a pharmaceutical candidate for its potential biological activity and reactivity. (2S)-2-[(Z)-[(5-chloro-2-hydroxy-phenyl)-phenyl-methylene]amino]-3-methyl-butanoic acid's diverse chemical functionalities and specific stereochemistry may contribute to its interactions with biological systems, making it a promising molecule for the development of new drugs and therapies.
Used in Chemical Research:
In the field of chemical research, (2S)-2-[(Z)-[(5-chloro-2-hydroxy-phenyl)-phenyl-methylene]amino]-3-methyl-butanoic acid serves as a valuable subject for studying the effects of stereochemistry on molecular interactions and reactivity. Its complex structure and functional groups provide opportunities for exploring various chemical reactions and mechanisms, contributing to the advancement of chemical knowledge and techniques.
Used in Material Science:
(2S)-2-[(Z)-[(5-chloro-2-hydroxy-phenyl)-phenyl-methylene]amino]-3-methyl-butanoic acid may also find applications in material science, where its unique structural features and chemical properties can be harnessed to develop new materials with specific properties. (2S)-2-[(Z)-[(5-chloro-2-hydroxy-phenyl)-phenyl-methylene]amino]-3-methyl-butanoic acid's potential to form complexes or interact with other molecules could be utilized in the design of novel materials for various applications, such as sensors, catalysts, or advanced materials with tailored properties.
Check Digit Verification of cas no
The CAS Registry Mumber 38075-43-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,0,7 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38075-43:
(7*3)+(6*8)+(5*0)+(4*7)+(3*5)+(2*4)+(1*3)=123
123 % 10 = 3
So 38075-43-3 is a valid CAS Registry Number.
38075-43-3Relevant articles and documents
Process for the preparation and purification of valgancyclovir
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Page/Page column 8, (2010/11/29)
A process for the preparation of valgancyclovir which comprises: a) reacting a compound of formula 7, in an aprotic solvent, in the presence of a condensing agent, with a compound of formula 8, wherein R1, and R2 may be, each independently, hydrogen, an halogen atom or an hydroxyl group; the double bond may either be in the E or Z configuration or a mixture thereof to yield a compound of formula 9 b) mild hydrolysis of compound obtained in a) to give valgancyclovir.
