Welcome to LookChem.com Sign In|Join Free

CAS

  • or

77658-97-0

Post Buying Request

77658-97-0 Suppliers

Recommended suppliersmore

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

77658-97-0 Usage

Originator

Anaxirone, Onbio Inc.

Uses

Triglycidylurazole is a drug shown to reduce tumor-induced bone destruction in the rat.

Manufacturing Process

In a 4-liter three-necked flask equipped with a stirrer, thermometer and reflux condenser, 101 g (1 mole) of triazolidine-3,5-dione, 2775 g (30 moles) of epichlorohydrin and 2 ml of triethylamine are heated to 80°C by means of an oil bath. The mixture reacts exothermically so that the oil bath may be removed. After the exothermic reaction has abated, the reaction mixture is stirred at 80°C. The total reaction time is 10 hours. 250 g of 50% sodium hydroxide solution are added dropwise to the solution obtained over a period of 4 hours at from 30 to 40°C in such a way that the water added and the water formed during the reaction is continuously removed by azeotropic distillation at from 30 to 60 Torr using a water separator. To complete the reaction, the reaction mixture is stirred for another hour and the sodium chloride formed is separated by filtration. The sodium chloride is washed twice with 200 g of epichlorohydrin and the combined epichlorohydrin solutions are washed with 200 ml of water. After the organic phase has been dried over sodium sulfate, the solvent is removed by concentration in a rotary evaporator and the residue is dried, ultimately at 80°C/0.2 mbar, to constant weight. 240 g of a light brown viscous oil are obtained. It was found to have an epoxide value of 0.93 and has a chlorine content of 2.75%. The viscous oil crystallizes after standing for from a few hours to days. The practically pure 1,2,4- triglycidyl triazolidine-3,5-dione melting at from 98° to 103°C crystallizes by dissolution in methanol and cooling to 5°C. IR- and NMR-spectra in conjunction with elemental analysis and epoxide determination confirm the assumed structure. Melting point 94-96°C.

Therapeutic Function

Antineoplastic

Check Digit Verification of cas no

The CAS Registry Mumber 77658-97-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,6,5 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 77658-97:
(7*7)+(6*7)+(5*6)+(4*5)+(3*8)+(2*9)+(1*7)=190
190 % 10 = 0
So 77658-97-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H15N3O5/c15-10-12(1-7-4-17-7)11(16)14(3-9-6-19-9)13(10)2-8-5-18-8/h7-9H,1-6H2

77658-97-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,4-tris(oxiran-2-ylmethyl)-1,2,4-triazolidine-3,5-dione

1.2 Other means of identification

Product number -
Other names EINECS 278-745-8

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:77658-97-0 SDS

77658-97-0Downstream Products

77658-97-0Relevant articles and documents

SYNTHESIS AND ANTITUMOR ACTIVITY OF EPOXY HETEROCYCLIC COMPOUNDS. 1. GLYCIDYL TRIAZOLONE AND IMIDAZOLONE DERIVATIVES

Korotkikh, N.I.,Losev, G.A.,Lipnitskii, V.F.,Kalistratov, S.G.,Sokolova, A.S.,Shvaika, O.P.

, p. 67 - 71 (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 77658-97-0