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7,7-dibromobicyclo[4.1.0]heptane is a halogenated organic compound with the molecular formula C7H10Br2. It features a bicyclic structure with seven carbon atoms, where the first ring has four carbons and the second ring has three carbons, connected at one carbon atom. The compound is characterized by the presence of two bromine atoms attached to the seventh carbon atom in each of the rings. This chemical is often used as an intermediate in the synthesis of various organic compounds, particularly in pharmaceuticals and agrochemicals, due to its unique structure and reactivity. It is important to handle 7,7-dibromobicyclo[4.1.0]heptane with care, as it may have potential health and environmental impacts, and is typically used in controlled laboratory settings.

2415-79-4

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2415-79-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2415-79-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,1 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2415-79:
(6*2)+(5*4)+(4*1)+(3*5)+(2*7)+(1*9)=74
74 % 10 = 4
So 2415-79-4 is a valid CAS Registry Number.

2415-79-4 Well-known Company Product Price

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  • Aldrich

  • (740640)  7,7-Dibromobicyclo[4.1.0]heptane  97%

  • 2415-79-4

  • 740640-1G

  • 568.62CNY

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2415-79-4SDS

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 7,7-dibromobicyclo[4.1.0]heptane

1.2 Other means of identification

Product number -
Other names 7,7-Dibromobicyclo<4.1.0>heptan

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

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More Details:2415-79-4 SDS

2415-79-4Relevant academic research and scientific papers

Reaction of diethyl dibromomalonate with methoxide: Evidence for a novel bromophilic attack

Mebane, Robert C.,Smith, Keegan M.,Rucker, Darlene R.,Foster, Michael P.

, p. 1459 - 1462 (1999)

Reaction of diethyl dibromomalonate (1) with sodium methoxide in cyclohexene yields dibromonorcarane (2) as the major product. This product forms via the capture of dibromocarbene (4) by cyclohexene. Dibromocarbene, in turn, is generated from ethyl tribromoacetate (6) which evidence suggests arises via a bromophilic attack between the carboethoxydibromomethyl carbanion (7) and diethyldibromomalonate (1).

gem-Dihalocyclopropane formation by iron/copper activation of tetrahalomethanes in the presence of nucleophilic olefins. Evidence for a carbene pathway

Léonel, Eric,Lejaye, Michael,Oudeyer, Sylvain,Paugam, Jean Paul,Nédélec, Jean-Yves

, p. 2635 - 2638 (2007/10/03)

The activation of CBr4 and CCl4 by a bimetallic iron/copper couple in acetonitrile is a new, inexpensive, nontoxic and efficient procedure for gem-dibromo- and gem-dichloromethylenation of nucleophilic alkenes. This new route to gem-dihalocyclopropanes involves dihalocarbene species.

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