Welcome to LookChem.com Sign In|Join Free

CAS

  • or

5435-96-1

Post Buying Request

5435-96-1 Suppliers

Recommended suppliersmore

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

5435-96-1 Usage

Composition

Piperazine ring with furan-2-ylcarbonyl group attached
Cyanomethoxy-3-methoxyphenylprop-2-enoate group

Structure

Cyclic structure due to piperazine ring
Functional groups: furan-2-ylcarbonyl and cyanomethoxy-3-methoxyphenylprop-2-enoate

Potential applications

Pharmaceuticals, research, industry

Unique properties

Requires further study and analysis for potential uses and properties

Check Digit Verification of cas no

The CAS Registry Mumber 5435-96-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,3 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5435-96:
(6*5)+(5*4)+(4*3)+(3*5)+(2*9)+(1*6)=101
101 % 10 = 1
So 5435-96-1 is a valid CAS Registry Number.

5435-96-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name hexaethyl propane-1,1,2,2,3,3-hexacarboxylate

1.2 Other means of identification

Product number -
Other names Propan-1,1,2,2,3,3-hexacarbonsaeure-hexaaethylester

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:5435-96-1 SDS

5435-96-1Downstream Products

5435-96-1Relevant articles and documents

Electrochemical oxidation of malonic esters in acetonitrile in the presence of iodides as mediators

Fedukovich,Elinson,Nikishin

, p. 599 - 602 (2007/10/03)

Electrochemical oxidation of malonic esters in acetonitrile in the presence of iodides follows two different pathways depending on the nature of the cation. In the presence of LiI, alkyl 1,1,2,2,3,3-propanetetracarboxylates were obtained in 85-98% yields. In the presence of NaI, KI, or Bu4NI, the formation of 1,1,2,2-ethanetetracarboxylates and their subsequent dehydrogenation to ethenetetracarboxylates was the main reaction pathway.

ELECTROCHEMICAL OXIDATION OF MALONIC ESTERS IN THE PRESENCE OF CATALYST CARRIERS - SALTS OF HYDRIODIC ACID

Elinson, M. N.,Fedukovich, S. K.,Nikishin, G. I.

, p. 2285 - 2289 (2007/10/02)

-

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 5435-96-1