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4443-39-4

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4443-39-4 Usage

General Description

PHT-DL-ASP-OH is a chemical compound with the molecular formula C11H13NO5. It is an amino acid derivative containing a phenylthio group and an aspartic acid residue. The compound has been studied for its potential pharmaceutical applications, particularly in the development of drugs for cancer and infectious diseases. PHT-DL-ASP-OH exhibits cytotoxic properties and has been investigated as a potential prodrug for targeted drug delivery. PHT-DL-ASP-OH shows promise as a tool in medicinal chemistry for the design of novel therapeutics with enhanced efficacy and reduced side effects.

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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