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37610-80-3

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37610-80-3 Usage

General Description

(1,3-Dioxolan-2-ylethyl)magnesium bromide is a chemical compound with the formula C6H11BrO2Mg. It is commonly used as a reagent in organic synthesis, especially in the formation of carbon-carbon bonds and the introduction of the (1,3-dioxolan-2-yl)ethyl group into organic molecules. (1,3-DIOXOLAN-2-YLETHYL)MAGNESIUM BROMIDE is highly reactive and must be handled with care due to its flammability and potential to react violently with water. It is often used in conjunction with other reagents and catalysts to carry out a variety of chemical reactions, and has found applications in the pharmaceutical and agrochemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 37610-80-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,6,1 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 37610-80:
(7*3)+(6*7)+(5*6)+(4*1)+(3*0)+(2*8)+(1*0)=113
113 % 10 = 3
So 37610-80-3 is a valid CAS Registry Number.

37610-80-3SDS

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 (2-(1,3-dioxolan-2-yl)ethyl)magnesium bromide

1.2 Other means of identification

Product number -
Other names [2-(1,3-dioxolan-2-yl)ethyl]magnesium 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:37610-80-3 SDS

37610-80-3Downstream Products

37610-80-3Relevant articles and documents

Enantioselective Synthesis of Cyclic Nitrones by Chemoselective Intramolecular Allylic Alkylation of Oximes

Sandmeier, Tobias,Carreira, Erick M.

supporting information, p. 9913 - 9918 (2021/03/29)

The enantio- and chemoselective iridium-catalyzed N-allylation of oximes is described for the first time. Intramolecular kinetic resolution provides access to cyclic nitrones and enantioenriched aliphatic allylic alcohols. Salient features of this transformation are its ability to employ E/Z-isomeric mixtures of oxime starting materials convergently and high functional group tolerance. The implementation of N-allylation/1,3-dipolar cycloaddition reaction sequences furnishes tricyclic isoxazolidines in highly enantio- and diastereoselective fashion. The synthetic utility of the approach is demonstrated by the efficient, formal synthesis of the marine natural product (+)-halichlorine.

DIAZASPIRODECANE OREXIN RECEPTOR ANTAGONISTS

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Page/Page column 27-28, (2008/06/13)

The present invention is directed to diazaspirodecane compounds which are antagonists of orexin receptors, and which are useful in the treatment or prevention of neurological and psychiatric disorders and diseases in which orexin receptors are involved. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which orexin receptors are involved.

An efficient synthesis of cholanic acids from 20-ketopregnanes

Fukumoto,Suzuki,Nemoto,et al.

, p. 3701 - 3704 (2007/10/02)

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