Welcome to LookChem.com Sign In|Join Free

CAS

  • or

66056-60-8

Post Buying Request

66056-60-8 Suppliers

Recommended suppliersmore

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

66056-60-8 Usage

Class

Cyclic imides

Structure

Pyrrolidin-2,4-dione

Usage

Manufacturing of pharmaceuticals, precursor in organic synthesis

Applications

Medicine, drug development

Characteristics

Interacts with biological macromolecules

Industry usage

Pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 66056-60-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,0,5 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 66056-60:
(7*6)+(6*6)+(5*0)+(4*5)+(3*6)+(2*6)+(1*0)=128
128 % 10 = 8
So 66056-60-8 is a valid CAS Registry Number.

66056-60-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Acetyltetramic acid

1.2 Other means of identification

Product number -
Other names 3-[1-Hydroxy-eth-(E)-ylidene]-pyrrolidine-2,4-dione

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:66056-60-8 SDS

66056-60-8Downstream Products

66056-60-8Relevant articles and documents

1,3-Dipolar cycloaddition route to nitrogen heterocyclic triones

Jones, Raymond C. F.,Bhalay, Gurdip,Carter, Paul A.,Duller, Kathryn A. M.,Dunn, Stephen H.

, p. 765 - 776 (2007/10/03)

1,3-Dipolar cycloaddition of nitrile oxides, formed in situ by dehydration of primary nitro compounds, with pyrrolidine enamines of protected γ- or δ-amino-β-keto esters affords isoxazole-4-carboxylates; these undergo lactam formation and N-O bond cleavage to afford 3-acyltetramic acids and 3-acyl-4-hydroxypyridin-2-ones.

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 66056-60-8