4443-39-4 Usage
Description
PHT-DL-ASP-OH is a chemical compound with the molecular formula C11H13NO5, characterized as an amino acid derivative featuring a phenylthio group and an aspartic acid residue. It has been the subject of research for its potential pharmaceutical applications, particularly in the development of drugs for cancer and infectious diseases. PHT-DL-ASP-OH is recognized for its cytotoxic properties and is being investigated as a prodrug for targeted drug delivery. It also holds promise as a valuable tool in medicinal chemistry for designing novel therapeutics with improved efficacy and minimized side effects.
Uses
Used in Pharmaceutical Industry:
PHT-DL-ASP-OH is used as a potential drug candidate for the development of therapeutics targeting cancer and infectious diseases due to its cytotoxic properties and potential as a prodrug for targeted drug delivery.
Used in Medicinal Chemistry:
PHT-DL-ASP-OH serves as a valuable tool for designing novel therapeutics with the aim of enhancing efficacy and reducing side effects in the treatment of various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 4443-39-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,4 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4443-39:
(6*4)+(5*4)+(4*4)+(3*3)+(2*3)+(1*9)=84
84 % 10 = 4
So 4443-39-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H9NO6/c14-9(15)5-8(12(18)19)13-10(16)6-3-1-2-4-7(6)11(13)17/h1-4,8H,5H2,(H,14,15)(H,18,19)
4443-39-4Relevant articles and documents
DESIGN AND SYNTHETIC APPLICATIONS OF NEW HETEROMETALLACYCLES
Echavarren, Antonio M.,Cardenas, Diego J.,Castano, Ana M.,Cuerva, Juan M.,Mateo, Cristina
, p. 549 - 558 (2007/10/02)
The reaction of cyclic anhydrides with Ni(0) complexes lead to the formation of nickelacycles by oxidative addition followed by decarbonylation.The preparation of chiral nickelacycles from anhydrides derived from amino acids and their reactivity is described.The formation of new heteropalladacycles by C-H activation or transmetallation reactions and their reactivity will be also discussed.
