13960-33-3

• 

• Basic information

  1. Product Name: 2-(4-nitrophenyl)-4,6-diphenyl-1,3,5-triazine
  2. Synonyms: 2-(P-NITROPHENYL)-4,6-DIPHENYL-S-TRIAZINE
  3. CAS NO:13960-33-3
  4. Molecular Formula: C₂₁H₁₄N₄O₂
  5. Molecular Weight: 354.3615
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 13960-33-3.mol
  9. Article Data: 11

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 609.8°C at 760 mmHg
  3. Flash Point: 322.6°C
  4. Appearance: N/A
  5. Density: 1.28g/cm³
  6. Vapor Pressure: 3.67E-14mmHg at 25°C
  7. Refractive Index: 1.649
  8. Storage Temp.: N/A
  9. Solubility: N/A
  10. CAS DataBase Reference: 2-(4-nitrophenyl)-4,6-diphenyl-1,3,5-triazine(CAS DataBase Reference)
  11. NIST Chemistry Reference: 2-(4-nitrophenyl)-4,6-diphenyl-1,3,5-triazine(13960-33-3)
  12. EPA Substance Registry System: 2-(4-nitrophenyl)-4,6-diphenyl-1,3,5-triazine(13960-33-3)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 13960-33-3(Hazardous Substances Data)

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• Downstream Products
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• 2-(4-Nitrophenyl)-4,6-Diphenyl-1,3,5-Triazine

  Cas No: 13960-33-3

• No Data

• 100 Gram

• 100 Metric Ton/Year

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13960-33-3 Usage

General Description

2-(4-nitrophenyl)-4,6-diphenyl-1,3,5-triazine is a chemical compound that belongs to the triazine family. It is a crystalline solid with a molecular formula C21H14N4O2 and a molecular weight of 350.36 g/mol. 2-(4-nitrophenyl)-4,6-diphenyl-1,3,5-triazine is often used in the field of organic chemistry and pharmaceutical research due to its unique structure and properties. It has been studied for its potential applications in organic synthesis and as a building block for the development of new pharmaceutical compounds. Additionally, 2-(4-nitrophenyl)-4,6-diphenyl-1,3,5-triazine has also been investigated for its potential biological activities, including its antibacterial and antifungal properties.

Check Digit Verification of cas no

The CAS Registry Mumber 13960-33-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,6 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13960-33:
(7*1)+(6*3)+(5*9)+(4*6)+(3*0)+(2*3)+(1*3)=103
103 % 10 = 3
So 13960-33-3 is a valid CAS Registry Number.

13960-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name	2-(4-nitrophenyl)-4,6-diphenyl-1,3,5-triazine

1.2 Other means of identification

Product number	-
Other names	2-(4-nitro-phenyl)-4,6-diphenyl-[1,3,5]triazine

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:13960-33-3 SDS

13960-33-3Upstream product

• 104-03-0 4-nitrobenzeneacetic acid 
• 1670-14-0 benzamidine monohydrochloride 
• 100-19-6 (4-nitrophenyl)ethanone 
• 7409-30-5 p-nitrobenzylamine 
• 99-99-0 1-methyl-4-nitrobenzene 
• 620-40-6 tribenzylamine 
• 15723-90-7 4-nitrobenzamidine hydrochloride 
• 619-73-8 4-nitrobenzyl chloride 
• 5496-39-9 2-(4-nitrophenyl)-4,5-diphenyl-1H-imidazole 

13960-33-3Downstream Products

13960-33-3Relevant articles and documents

-

Silversmith

, p. 3568 (1963)

-

Transition Metal-Free sp3 C–H Functionalization of Arylacetic Acids for the Synthesis of 1,3,5-Triazines

Pardeshi, Sachin D.,Sathe, Pratima A.,Pawar, Balu V.,Vadagaonkar, Kamlesh S.,Chaskar, Atul C.

, p. 2098 - 2102 (2018/05/31)

A one-pot simple, efficient and practically viable protocol for the synthesis of substituted 1,3,5-triazines has been reported from arylacetic acids and benzamidine hydrochloride. In addition, we demonstrated first transition metal-free conversion of phenylacetic acid to benzaldehyde which on condensation with two equivalents of benzamidine hydrochloride offered 2,4,6-trisubstituted 1,3,5-triazines. This protocol is environmentally benign and economically viable which makes it feasible for gram scale synthesis.

Iridium-catalyzed cascade dehydrogenation, ring-closure reaction leading to 2,4,6-triaryl-1,3,5-triazines

Shi, Gang,He, Fei,Che, Youxin,Ni, Caihua,Li, Ying

, p. 380 - 386 (2016/04/20)

An efficient iridium-catalyzed dehydrogenation, ring-closure reaction, has been developed via a cascade sequence, in which [Cp?IrI2]2/Xantphos proved to be the most efficient catalyst for the synthesis of 2,4,6-triaryl-1,3,5-triazines from stable aryl-substituted alcohols and amidines. It was the first case of iridium catalyst successful application in such transformation.

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