Welcome to LookChem.com Sign In|Join Free

CAS

  • or

2294-43-1

Post Buying Request

2294-43-1 Suppliers

Recommended suppliersmore

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

2294-43-1 Usage

Family

Benzene family

Contains

a. Bromine atom
b. Prop-2-enyl group on the benzene ring

Usage

a. Intermediate in organic synthesis
b. Production of pharmaceuticals and agrochemicals
c. Manufacturing of fragrances and flavors

Potential applications

a. Field of organic chemistry
b. Synthesis of various organic compounds

Safety precautions

Handle with care due to potential health and safety hazards

Check Digit Verification of cas no

The CAS Registry Mumber 2294-43-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,9 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2294-43:
(6*2)+(5*2)+(4*9)+(3*4)+(2*4)+(1*3)=81
81 % 10 = 1
So 2294-43-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H9Br/c1-2-3-8-4-6-9(10)7-5-8/h2,4-7H,1,3H2

2294-43-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-bromo-4-prop-2-enylbenzene

1.2 Other means of identification

Product number -
Other names 3-(4-Bromophenyl)-1-propene

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:2294-43-1 SDS

2294-43-1Relevant articles and documents

Synthesis of new cellulose ethers using Suzuki-Miyaura reactions

Goncalves, Cédric,Favre, Camille,Feuardant, Pierre,Klein, Sarah,Vaca-Garcia, Carlos,Cecutti, Christine,Thiébaud-Roux, Sophie,Vedrenne, Emeline

, p. 51 - 59 (2014)

Cellulose ethers are functionalized biopolymers that are industrially produced through drastic conditions employing gaseous reactants with a high risk of industrial accident. The cellulose ethers that are commercially available generally bear short carbon-chains. In this work, an alternative method using non-gaseous chemicals is proposed. It relies on the use of the Suzuki-Miyaura reaction employing mild, moisture- and air-stable conditions. Relatively innocuous reagents are used for this step, which allows the formation of a wide range of cellulose ethers bearing various functional groups with different chain-length.

Catalytic, contra-Thermodynamic Positional Alkene Isomerization

Occhialini, Gino,Palani, Vignesh,Wendlandt, Alison E.

supporting information, p. 145 - 152 (2022/01/19)

The positional isomerization of C═C double bonds is a powerful strategy for the interconversion of alkene regioisomers. However, existing methods provide access to thermodynamically more stable isomers from less stable starting materials. Here, we report

MIDA boronate allylation-synthesis of ibuprofen

Brodie, Glen,France, David J.,Memarzadeh, Sarah,Phillips, David,Tang, Gi Lum

, p. 30624 - 30630 (2020/09/11)

MIDA boronates are among the most useful reagents for the Suzuki-Miyaura reaction. This chemistry typically generates new bonds between two aromatic rings, thereby restricting access to important areas of chemical space. Here we demonstrate the coupling of MIDA boronates to allylic electrophiles, including a new synthesis of the well-known COX inhibitor ibuprofen. This journal is

Palladium-Catalyzed Oxidative Allylation of Sulfoxonium Ylides: Regioselective Synthesis of Conjugated Dienones

Li, Chunsheng,Li, Meng,Zhong, Wentao,Jin, Yangbin,Li, Jianxiao,Wu, Wanqing,Jiang, Huanfeng

supporting information, p. 872 - 875 (2019/05/16)

The first examples of palladium-catalyzed allylic C-H oxidative allylation of sulfoxonium ylides to afford the corresponding conjugated dienones with moderate to good yields have been established. The features of this novel conversion include mild reaction conditions, wide substrate scope, and excellent regioselectivity.

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 2294-43-1