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39691-62-8

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39691-62-8 Usage

General Description

. Nonylmagnesium bromide 1.0M solution is a chemical compound that consists of nonyl (C9H19) groups attached to a magnesium atom through a bromide bond. It is commonly used as a reagent in organic synthesis and as a catalyst in various chemical reactions. Nonylmagnesium bromide 1.0M solution is known for its ability to facilitate Grignard reactions, which involve the addition of an alkyl or aryl group to a carbonyl compound. NONYLMAGNESIUM BROMIDE 1.0M SOLUTION I& is typically stored in a nonpolar solvent such as tetrahydrofuran (THF) to prevent it from reacting with moisture or air. Nonylmagnesium bromide 1.0M solution is considered a highly reactive and potent reagent and should be handled with care under appropriate safety measures.

Check Digit Verification of cas no

The CAS Registry Mumber 39691-62-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,6,9 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 39691-62:
(7*3)+(6*9)+(5*6)+(4*9)+(3*1)+(2*6)+(1*2)=158
158 % 10 = 8
So 39691-62-8 is a valid CAS Registry Number.

39691-62-8SDS

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 NONYLMAGNESIUM BROMIDE 1.0M SOLUTION I&

1.2 Other means of identification

Product number -
Other names nonylmagnesium 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:39691-62-8 SDS

39691-62-8Relevant articles and documents

Towards enantioselective adsorption in surface-confined nanoporous systems

Ghijsens, Elke,Cao, Hai,Noguchi, Aya,Ivasenko, Oleksandr,Fang, Yuan,Tahara, Kazukuni,Tobe, Yoshito,De Feyter, Steven

, p. 4766 - 4769 (2015)

The adsorption of chiral molecules in surface-confined chiral porous networks shows pronounced selectivity, as a result of complementary host-guest interactions. This journal is

IRON CATALYZED CROSS-COUPLING REACTIONS OF ACYL CHLORIDES WITH GRIGNARD REAGENTS. A MILD, GENERAL, AND CONVENIENT SYNTHESIS OF ALIPHATIC AND AROMATIC KETONES.

Fiandanese, V.,Marchese, G.,Martina, V.,Ronzini, L.

, p. 4805 - 4808 (2007/10/02)

Acyl chlorides couple with Grignard reagents at room temperature in the presence of catalytic amounts of tris(acetylacetonate)iron(III), Fe(acac)3.The reaction is general with respect to both reactants and provides a very mild and convenient method for the synthesis of aliphatic and aromatic ketones.

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