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ALLYL-2-D1 BROMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60468-26-0

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60468-26-0 Usage

Properties

1. Synthetic chemical compound
2. Composed of bromine and allyl
3. Used in organic synthesis
4. Acts as a halogenating agent
5. Effective in introducing bromine atoms into organic molecules
6. Used in pharmaceutical and agrochemical industries
7. Building block for synthesis of complex chemical compounds

Composition

bromine and allyl

Uses

organic synthesis, reagent in chemical reactions, halogenating agent, pharmaceutical industry, agrochemical production

Role

crucial in development and production of chemical products

Check Digit Verification of cas no

The CAS Registry Mumber 60468-26-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,6 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 60468-26:
(7*6)+(6*0)+(5*4)+(4*6)+(3*8)+(2*2)+(1*6)=120
120 % 10 = 0
So 60468-26-0 is a valid CAS Registry Number.

60468-26-0SDS

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 ALLYL-2-D1 BROMIDE

1.2 Other means of identification

Product number -
Other names 3-Brom-cyclohexen-2-on

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:60468-26-0 SDS

60468-26-0Upstream product

60468-26-0Downstream Products

60468-26-0Relevant academic research and scientific papers

Evidence for alkene cis-aminocupration, an aminooxygenation case study: Kinetics, EPR spectroscopy, and DFT calculations

Paderes, Monissa C.,Belding, Lee,Fanovic, Branden,Dudding, Travis,Keister, Jerome B.,Chemler, Sherry R.

supporting information; experimental part, p. 1711 - 1726 (2012/04/10)

Alkene difunctionalization reactions are important in organic synthesis. We have recently shown that copper(II) complexes can promote and catalyze intramolecular alkene aminooxygenation, carboamination, and diamination reactions. In this contribution, we

Nickel-catalyzed cycloisomerization of enynes: catalyst generation via C-H activation of carbene ligands

Tekavec, Thomas N.,Louie, Janis

, p. 6870 - 6875 (2008/09/21)

The combination of Ni(0) and an N-heterocyclic carbene acts as a precatalyst for the cycloisomerization of enynes to afford 1,3-dienes. During the course of the reaction, a nickel hydride is formed from oxidative addition of the ortho C-H on the carbene ligand. Deuterium labeling studies are presented. Crown Copyright

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