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1919-48-8

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1919-48-8 Usage

Chemical Properties

OFF-WHITE TO LIGHT BEIGE FLUFFY POWDER

Uses

2,4,6-Triphenoxy-1,3,5-triazine was used to study the steric structure effects in the triazine system for formation of polymeric structures.

Check Digit Verification of cas no

The CAS Registry Mumber 1919-48-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,1 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1919-48:
(6*1)+(5*9)+(4*1)+(3*9)+(2*4)+(1*8)=98
98 % 10 = 8
So 1919-48-8 is a valid CAS Registry Number.
InChI:InChI=1/C21H15N3O3/c1-4-10-16(11-5-1)25-19-22-20(26-17-12-6-2-7-13-17)24-21(23-19)27-18-14-8-3-9-15-18/h1-15H

1919-48-8 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
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  • Detail
  • Alfa Aesar

  • (H33572)  2,4,6-Triphenoxy-1,3,5-triazine, 96%   

  • 1919-48-8

  • 10g

  • 260.0CNY

  • Detail
  • Alfa Aesar

  • (H33572)  2,4,6-Triphenoxy-1,3,5-triazine, 96%   

  • 1919-48-8

  • 50g

  • 1042.0CNY

  • Detail
  • Aldrich

  • (153664)  2,4,6-Triphenoxy-1,3,5-triazine  98%

  • 1919-48-8

  • 153664-10G

  • 460.98CNY

  • Detail

1919-48-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-TRIPHENOXY-1,3,5-TRIAZINE

1.2 Other means of identification

Product number -
Other names EINECS 217-644-5

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:1919-48-8 SDS

1919-48-8Relevant articles and documents

-

Gibson,Murray

, p. 880 (1965)

-

Choline Hydroxide as a Versatile Medium for Catalyst-Free O-Functionalization of Phenols

Joo, Seong-Ryu,Kim, Seung-Hoi,Kwon, Gyu-Tae,Park, Soo-Youl

, p. 1200 - 1205 (2020/11/30)

A versatile synthetic protocol for benzyl phenyl ether preparation via O-alkylation of phenolic oxygen with readily available benzyl derivatives was demonstrated. The newly designed procedure was carried out using an eco-friendly medium, room-temperature ionic liquid (choline hydroxide), under metal- and base-catalyst-free aerobic conditions. The reaction platform was also successfully applied to phenol protection strategy.

Nickel-catalyzed reductive amidation of aryl-triazine ethers

Heravi, Majid M.,Panahi, Farhad,Iranpoor, Nasser

supporting information, p. 1992 - 1995 (2020/02/22)

The reaction of activated phenolic compounds, 2,4,6-triaryloxy-1,3,5-triazine (aryl-triazine ethers), with various isocyanates or carbodiimides in the presence of a nickel pre-catalyst resulted in the synthesis of aryl amides in good to excellent yields.

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