Welcome to LookChem.com Sign In|Join Free
  • or
"Benzene, 1,1'-(1-propenylidene)bis[4-chloro-" is a complex organic chemical compound, characterized by its unique structure. It is a derivative of benzene, with two 4-chloro substituents attached to the 1 and 1' positions. The key feature of Benzene, 1,1'-(1-propenylidene)bis[4-chloro- is the 1-propenylidene bridge that connects the two benzene rings, creating a rigid structure. Benzene, 1,1'-(1-propenylidene)bis[4-chloro- is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its reactive sites and the presence of chlorine atoms, which can be further functionalized. It is important to handle Benzene, 1,1'-(1-propenylidene)bis[4-chloro- with care due to its potential reactivity and the presence of chlorine, which can pose environmental and health concerns if not managed properly.

3439-04-1

Post Buying Request

3439-04-1 Suppliers

Recommended suppliers

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

3439-04-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3439-04-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,3 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3439-04:
(6*3)+(5*4)+(4*3)+(3*9)+(2*0)+(1*4)=81
81 % 10 = 1
So 3439-04-1 is a valid CAS Registry Number.

3439-04-1Relevant academic research and scientific papers

Regioselective Diboron-Mediated Semireduction of Terminal Allenes

Gates, Ashley M.,Santos, Webster L.

, p. 4619 - 4624 (2019/12/11)

A method for the regioselective reduction of the terminal double bond of 1,1-disubstituted allenes has been developed. In the presence of a palladium catalyst, tetrahydroxydiboron and stoichiometric water, allene semireduction proceeds in high yield to afford Z-alkenes selectively.

Iron-catalyzed decarboxylative methylation of α,β-unsaturated acids under ligand-free conditions

Rong, Guangwei,Liu, Defu,Lu, Linhua,Yan, Hong,Zheng, Yang,Chen, Jie,Mao, Jincheng

, p. 5033 - 5037 (2014/12/10)

It is the first time to find that iron-catalyzed decarboxylative methylation of α,β-unsaturated acids could be performed in the absence of any ligands. During the reaction, the configuration of the double bond could be retained. It is noteworthy that di-t

Iron-catalyzed decarboxylative methylation of α,β-unsaturated acids under ligand-free conditions

Rong, Guangwei,Liu, Defu,Lu, Linhua,Yan, Hong,Zheng, Yang,Chen, Jie,Mao, Jincheng

, p. 5033 - 5037 (2014/07/08)

It is the first time to find that iron-catalyzed decarboxylative methylation of α,β-unsaturated acids could be performed in the absence of any ligands. During the reaction, the configuration of the double bond could be retained. It is noteworthy that di-t

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 3439-04-1