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5398-65-2

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5398-65-2 Usage

Physical state

Colorless liquid

Odor

Pungent

Classification

Halogenated organic compound

Structure

Cyclopropane derivative with two bromine atoms and a vinyl group

Uses

Intermediate in the synthesis of various organic compounds, reagent in organic synthesis, building block for specialty chemicals

Safety

Handle with care, follow proper safety protocols due to halogenated nature

Check Digit Verification of cas no

The CAS Registry Mumber 5398-65-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,9 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5398-65:
(6*5)+(5*3)+(4*9)+(3*8)+(2*6)+(1*5)=122
122 % 10 = 2
So 5398-65-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H6Br2/c1-2-4-3-5(4,6)7/h2,4H,1,3H2

5398-65-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-vinyl-1,1-dibromocyclopropane

1.2 Other means of identification

Product number -
Other names 1,1-Dibromo-2-ethenylcyclopropane

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:5398-65-2 SDS

5398-65-2Relevant articles and documents

Enantiomerically pure 2,2-dibromocyclopropanecarboxylic acids, simple chiral building blocks

Baird, Mark S.,Licence, Peter,Tverezovsky, Viacheslav V.,Bolesov, Ivan G.,Clegg, William

, p. 2773 - 2784 (1999)

Simple chiral building blocks 1-(R)- and 1-(S)-2,2- dibromocyclopropanecarboxylic acids and 2-(R)-bromo-1-(S')- cyclopropanecarboxylic acids and their 1-methyl analogues, have been obtained on a preparatively useful laboratory scale.

Thermodynamic control of diastereoselectivity in the formal nucleophilic substitution of bromocyclopropanes

Banning, Joseph E.,Prosser, Anthony R.,Rubin, Michael

supporting information; experimental part, p. 1488 - 1491 (2010/06/21)

(Figure Presented) A new, general, and chemoselective protocol for the formal nucleophilic substitution of 2-bromocyclopropylcarboxamides is described. A wide range of alcohols and phenols can be employed as pronucleophiles in this transformation, providi

Synthese von funktionalisierten bi(cyclopropylidenen)

Huwyler, Rolf,Al-Dulayymi, Ahmad,Neuenschwander, Markus

, p. 2336 - 2347 (2007/10/03)

In view of the synthesis of attractive triafulvalene precursors 9, a series of bi(cyclopropylidenes) 8 with vinyl(8a), alkoxycarbonyl (8c-f), hydroxymethyl (8h), as well as protected hydroxymethyl groups (8g, 8i) have been prepared by simple one-pot react

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