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319918-15-5

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319918-15-5 Usage

Description

2-(Allyloxy)benzyl bromide, with the molecular formula C10H11BrO, is a brominated benzyl ether that features an allyl group. It is a significant building block in organic chemistry, known for its versatile reactivity and structural properties. 2-(Allyloxy)benzyl BroMide is utilized in various applications, including the synthesis of pharmaceutical and agrochemical intermediates, as well as the production of specialty chemicals. However, due to its toxic and potentially hazardous nature, careful handling is required.

Uses

Used in Organic Synthesis:
2-(Allyloxy)benzyl bromide is used as a reagent for the introduction of the benzyl bromide functional group in organic synthesis. Its ability to easily introduce this functional group makes it a valuable tool in the creation of a wide range of organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(Allyloxy)benzyl bromide is used as a key intermediate in the preparation of various pharmaceutical compounds. Its unique structure and reactivity contribute to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 2-(Allyloxy)benzyl bromide serves as an important intermediate for the synthesis of agrochemicals. Its role in creating effective and targeted agrochemicals is vital for agricultural productivity and pest control.
Used in Specialty Chemicals Manufacturing:
2-(Allyloxy)benzyl bromide is also utilized in the manufacturing of specialty chemicals, where its unique properties allow for the production of high-quality and specialized chemical products for various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 319918-15-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,9,9,1 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 319918-15:
(8*3)+(7*1)+(6*9)+(5*9)+(4*1)+(3*8)+(2*1)+(1*5)=165
165 % 10 = 5
So 319918-15-5 is a valid CAS Registry Number.

319918-15-5SDS

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-(bromomethyl)-2-(prop-2-en-1-yloxy)benzene

1.2 Other means of identification

Product number -
Other names 2-(Allyloxy)benzyl Bromide

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:319918-15-5 SDS

319918-15-5Relevant articles and documents

Tetrahydrobenzochromene Synthesis Enabled by a Deconjugative Alkylation/Tsuji-Saegusa-Ito Oxidation on Knoevenagel Adducts

Navaratne, Primali V.,Grenning, Alexander J.

, p. 4566 - 4570 (2018/08/09)

A modular and practical route to versatile cyano-1,3-dienes by a sequence involving deconjugative alkylation and "Tsuji-Saegusa-Ito oxidation" is reported. In this letter, the versatility of the products is also explored, including a route to benzochromene scaffolds common to many natural products.

Rhodium-catalyzed cycloisomerization involving cyclopropenes: Efficient stereoselective synthesis of medium-sized heterocyclic scaffolds

Miege, Frederic,Meyer, Christophe,Cossy, Janine

supporting information; experimental part, p. 5932 - 5937 (2011/08/02)

A happy medium: The title reaction of cyclopropenyl carbinols and carbinylamines gives carbo- and heterocycles with a [6.1.0] bicyclic ring fused to an aromatic ring (see scheme, Alloc=allyloxycarbonyl, Boc=tert- butyloxycarbonyl). These reactions are the first examples of the formation of medium-sized rings by the intramolecular cyclopropanation of an alkene with a donor-substituted rhodium carbenoid, which is not generated from a diazo compound.

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