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4443-39-4

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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)

4443-39-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1,3-dioxoisoindol-2-yl)butanedioic acid

1.2 Other means of identification

Product number -
Other names N,N-phthaloyl-aspartic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4443-39-4 SDS

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.

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