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703591

Sigma-Aldrich

Ethylmagnesiumbromid -Lösung

greener alternative

3.4 M in 2-methyltetrahydrofuran

Synonym(e):

Bromoethylmagnesium

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About This Item

Lineare Formel:
CH3CH2MgBr
CAS-Nummer:
925-90-6
Molekulargewicht:
133.27
Beilstein:
3587203
MDL-Nummer:
MFCD00000043
UNSPSC-Code:
12352103
PubChem Substanz-ID:
329762053
NACRES:
NA.22

Form

liquid

Eignung der Reaktion

reaction type: Grignard Reaction

Grünere Alternativprodukt-Eigenschaften

Safer Solvents and Auxiliaries
Use of Renewable Feedstocks
Inherently Safer Chemistry for Accident Prevention
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

Konzentration

3.4 M in 2-methyltetrahydrofuran
40 % (w/w)

Dichte

1.142 g/mL at 25 °C

Grünere Alternativprodukt-Kategorie

, Aligned

SMILES String

CC[Mg]Br

InChI

1S/C2H5.BrH.Mg/c1-2;;/h1H2,2H3;1H;/q;;+1/p-1

InChIKey

TWTWFMUQSOFTRN-UHFFFAOYSA-M

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Allgemeine Beschreibung

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product, 1.0 M in 2-methyltetrahydrofuran aligns with Safer Solvents and Auxiliaries, Use of Renewable Feedstocks and Inherently Safer Chemistry for Accident Prevention. Click here for more information.

Anwendung

Grignard reagent in greener solvent, 2-methyltetrahydrofuran (2-MeTHF)

2-Methyltetrahydrofuran (2-MeTHF): A Biomass-Derived Solvent with Broad Application in Organic Chemistry

Rechtliche Hinweise

Chemetall Product

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - Water-react 1

Zusätzliche Gefahrenhinweise

EUH014,EUH019

Lagerklassenschlüssel

4.3 - Hazardous materials which set free flammable gases upon contact with water

WGK

WGK 2

Flammpunkt (°F)

24.8 °F - closed cup

Flammpunkt (°C)

-4 °C - closed cup

Persönliche Schutzausrüstung

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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2-Methyltetrahydrofuran BioRenewable, anhydrous, ≥99.0%, contains 250 ppm BHT as stabilizer

Sigma-Aldrich

414247

2-Methyltetrahydrofuran

2-Methyltetrahydrofuran BioRenewable, anhydrous, ≥99%, Inhibitor-free

Sigma-Aldrich

673277

2-Methyltetrahydrofuran

Titan(IV)isopropoxid 97%

Sigma-Aldrich

205273

Titan(IV)isopropoxid

Janne E Tønder et al.
Organic & biomolecular chemistry, 2(10), 1447-1455 (2004-05-12)
Copper mediated allylic substitutions and conjugate additions to geranyl, cinnamyl and allylic indole compounds have been investigated with the aim of finding a method for the creation of the all-carbon quaternary centre present in the natural product lyngbyatoxin A. Reaction
T Nishiyama et al.
Chemical & pharmaceutical bulletin, 48(12), 1999-2002 (2001-01-06)
The direct alpha-bromination of various ketones using trifluoromethanesulfonic anhydride and Grignard reagent or magnesium bromide in ether gave the corresponding alpha-bromo ketones in moderate to good yields under mild reaction conditions.
F Turon et al.
Lipids, 37(8), 817-821 (2002-10-10)
An analytical procedure was developed for regiodistribution analysis of TAG using alpha-MAG prepared by an ethyl magnesium bromide deacylation. In the present communication, the deacylation procedure is shown to lead to representative alpha-MAG, allowing the composition of the native TAG
R G Xie et al.
Steroids, 55(11), 488-490 (1990-11-01)
The reaction of ethyl magnesium bromide and 17 alpha-ethynylestradiol with formaldehyde in the presence of triethyl phosphate or hexamethylphosphoramide gave the 2- and 4-formyl-17 alpha-ethynylestradiol in high yield. Treatment of the formyl derivatives with an alkaline solution of hydrogen peroxide
Yuichi Kobayashi et al.
Organic letters, 7(2), 183-186 (2005-01-14)
[Reaction: see text] Low regioselectivity of RMgBr (R = aryl, alkenyl) in the CuCN-catalyzed reaction with 4-cyclopentene-1,3-diol monoacetate is improved by addition of LiCl or MgCl2 to a similar extent as previously obtained with RMgCl (>90:10). The limitation encountered in
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