Welcome to LookChem.com Sign In|Join Free
  • or
Benzene, 1,4-bis(1-phenylethenyl)-, also known as 1,4-bis(1-phenylethenyl)benzene or 1,4-diphenyl-1,3-butadiene, is an organic compound with the chemical formula C20H18. It is a symmetrical molecule consisting of a central benzene ring with two phenyl groups attached to the 1 and 4 positions, each connected to a vinyl group. Benzene, 1,4-bis(1-phenylethenyl)- is an important intermediate in the synthesis of various organic compounds, particularly in the production of polymers and pharmaceuticals. It is known for its aromatic character and conjugated double bonds, which contribute to its unique chemical properties and reactivity. The compound is typically synthesized through various methods, including the reaction of benzene with butadiene in the presence of a catalyst. Due to its potential applications and chemical versatility, it is a subject of interest in organic chemistry research.

1605-19-2

Post Buying Request

1605-19-2 Suppliers

Recommended suppliers

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

1605-19-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1605-19-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1605-19:
(6*1)+(5*6)+(4*0)+(3*5)+(2*1)+(1*9)=62
62 % 10 = 2
So 1605-19-2 is a valid CAS Registry Number.

1605-19-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-bis(1-phenylethenyl)benzene

1.2 Other means of identification

Product number -
Other names Ph(4-(Ph)C(CH2)C6H3)CCH2

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:1605-19-2 SDS

1605-19-2Downstream Products

1605-19-2Relevant academic research and scientific papers

Direct synthesis of 1,1-diarylalkenes from alkenyl phosphates via nickel(0)-catalysed Suzuki-Miyaura coupling

Hansen, Anders L.,Ebran, Jean-Philippe,Gogsig, Thomas M.,Skrydstrup, Troels

, p. 4137 - 4139 (2007/10/03)

A combination of Ni(COD)2 and PCy3 promotes effectively the Suzuki-Miyaura cross coupling of 1-arylalkenyl phosphates with aryl boronic acids with yields attaining 99%. The Royal Society of Chemistry 2006.

Electron delocalization in cross-conjugated p-phenylenevinylidene oligomers

Klokkenburg, Mark,Lutz, Martin,Spek, Anthony L.,Van der Maas, John H.,Van Walree, Cornelis A.

, p. 3544 - 3554 (2007/10/03)

The synthesis, structure, and electronic properties of a series of cross-conjugated p-phenylenevinylidene oligomers with one to four double bonds are reported. The X-ray crystal structure of the compound with two double bonds reveals a nonplanar conformat

Multifunctional lithium containing initiator

-

, (2008/06/13)

Highly desirable multifunctional lithium containing initiators are prepared by reacting a compound such as an organo lithium with an organic compound containing at least two 1,1-diphenylethylene groups. Such initiators can be prepared in the absence of polar solvents and are very desirable for the polymerization of dienes such as butadiene to a desirable 1,4 configuration. Several di-lithium compounds have been employed to initiate polymerization of various unsaturated organic monomers.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1605-19-2