Welcome to LookChem.com Sign In|Join Free

CAS

  • or

75001-09-1

Post Buying Request

75001-09-1 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

75001-09-1 Usage

General Description

2-[2-(2-Phthalimidoethoxy)ethoxy]acetic acid, also known as Daunomycinone, is a chemical compound with the formula C14H15NO6. 2-[2-(2-Phthalimidoethoxy)ethoxy]acetic acid generally features a cyclic structure known as a phthalimide group. Phthalimides are commonly used in the generation of a variety of pharmaceutical substances due to their useful properties. They are typically known for their ability to aid in the treatment of diseases such as cancer or HIV. This specific chemical, 2-[2-(2-Phthalimidoethoxy)ethoxy]acetic acid, has notable use in the production of medicines and therapeutic compounds. The compound's behavior in biological settings or additional potential uses are in continuous research study and investigation.

Check Digit Verification of cas no

The CAS Registry Mumber 75001-09-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,0,0 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75001-09:
(7*7)+(6*5)+(5*0)+(4*0)+(3*1)+(2*0)+(1*9)=91
91 % 10 = 1
So 75001-09-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H15NO6/c16-12(17)9-21-8-7-20-6-5-15-13(18)10-3-1-2-4-11(10)14(15)19/h1-4H,5-9H2,(H,16,17)

75001-09-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(2-Phthalimidoethoxy)ethoxy]acetic acid

1.2 Other means of identification

Product number -
Other names 3,6-Dioxa-8-phthalimidooctanoic 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:75001-09-1 SDS

75001-09-1Downstream Products

75001-09-1Relevant articles and documents

Preparation method of precursor raw material Pht-AEEA-AEEA for somatostatin side chain

-

Paragraph 0047; 0057-0059; 0083; 0093-0095; 0119; 0129-0131, (2021/10/05)

The preparation method comprises the following steps: in the reaction kettle, adding AEEA phthalic AEEA anhydride, toluene, opening stirring, heating and refluxing, separating the 100 ml water Pht through a water separator, ending the reaction, and lowering the temperature to room temperature. Post-treatment: addition of saturated NaHCO3 The solution was washed 1h. The method is scientific and reasonable in structure, safe and convenient to use, and safe and convenient to use; the product is prepared by using @timetime@ petroleum ether 1:20, AEEA-AEEA ethyl ester as a raw material, PA-AEEA - ethyl ester preparation third and deamination, and then PA ethyl ester is prepared by using the solid phase method AEEA AEEA . 4th-Pht-AEEA Ethyl AEEA -ethyl ester.

Synthesis of novel amphiphilic spin probes with the paramagnetic doxyl group in the polar region

Pajk, Stane,Pe?ar, Slavko

scheme or table, p. 659 - 665 (2009/04/07)

The use of ESR and specially designed spin probes has led to major breakthroughs in understanding the complexity of biological membranes. Research has been focused mainly on molecular events within the?lipid bilayer, and few probes have been designed for studying events in the extracellular space near the membrane surface. We have prepared a series of amphiphilic spin probes in which an ethylene glycol type hydrophilic spacer was introduced between a hydrophobic anchor and the doxyl group, placing the latter above the membrane in the extracellular space. Furthermore, the 2pπ orbital, containing the unpaired electron of the nitroxide group, would be orientated perpendicular to the membrane surface, making it more useful for ESR investigations of structural and dynamic properties close to the membrane surface in different situations of the cell life.

THE SYNTHESIS OF GLYCOLIPIDS CONTAINING A HYDROPHILIC SPACER-GROUP

Slama, James,Rando, Robert R.

, p. 213 - 222 (2007/10/02)

Cholesterol-containing glycolipids incorporating a new hydrophilic specer-group, 8-amino-3,6-dioxaoctanoic acid, were synthesized.This spacer group eliminates many of the problems inherent in the use of hydrophobic or charged, spacer arms.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 75001-09-1