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87280-01-1

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87280-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87280-01-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,8 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 87280-01:
(7*8)+(6*7)+(5*2)+(4*8)+(3*0)+(2*0)+(1*1)=141
141 % 10 = 1
So 87280-01-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H11BrO/c1-2-7-12-8-9-5-3-4-6-10(9)11/h2-6H,1,7-8H2

87280-01-1 Well-known Company Product Price

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  • Aldrich

  • (586897)  Allyl2-bromobenzylether  95%

  • 87280-01-1

  • 586897-1G

  • 510.12CNY

  • Detail

87280-01-1SDS

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-2-(prop-2-enoxymethyl)benzene

1.2 Other means of identification

Product number -
Other names allyl o-bromobenzyl ether

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:87280-01-1 SDS

87280-01-1Relevant articles and documents

A Short and Efficient Synthesis of the [3]Triangulene Ring System

Holt, Carter J.,Wentworth, Katelyn J.,Johnson, Richard P.

, p. 15793 - 15796 (2019)

Triangulenes are of current interest for potential applications in molecular electronics. We describe here a three step synthesis of the 4,8,12-trihydro[3]triangulenium cation by cascade cyclization of a tetra-benzyl alcohol precursor in triflic acid solu

Electrochemical Vicinal Difluorination of Alkenes: Scalable and Amenable to Electron-Rich Substrates

Doobary, Sayad,Sedikides, Alexi T.,Caldora, Henry P.,Poole, Darren L.,Lennox, Alastair J. J.

supporting information, p. 1155 - 1160 (2019/12/11)

Fluorinated alkyl groups are important motifs in bioactive compounds, positively influencing pharmacokinetics, potency and conformation. The oxidative difluorination of alkenes represents an important strategy for their preparation, yet current methods are limited in their alkene-types and tolerance of electron-rich, readily oxidized functionalities, as well as in their safety and scalability. Herein, we report a method for the difluorination of a number of unactivated alkene-types that is tolerant of electron-rich functionality, giving products that are otherwise unattainable. Key to success is the electrochemical generation of a hypervalent iodine mediator using an “ex-cell” approach, which avoids oxidative substrate decomposition. The more sustainable conditions give good to excellent yields in up to decagram scales.

Selectivity in the tandem cyclization - Carboxylation reaction of unsaturated haloaryl ethers catalyzed by electrogenerated nickel complexes

Olivero,Du?ach

, p. 1885 - 1891 (2007/10/03)

The electrochemical reduction of a series of 2-haloaryl ethers containing allyl and propargyl groups under CO2 allows the synthesis of benzofuranacetic acid derivatives. This novel intramolecular cyclization- carboxylation reaction is carried out in single-compartment cells and is catalyzed by [Ni(cyclam)Br2].

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