Skip to Content
Merck
All Photos(1)

Key Documents

256021

Sigma-Aldrich

(Trimethylsilyl)methylmagnesium chloride solution

1.0 M in diethyl ether

Synonym(s):

(Trimethylsilyl)methyl magnesium chloride, Chloro(trimethylsilylmethyl)magnesium

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(CH3)3SiCH2MgCl
CAS Number:
Molecular Weight:
146.97
Beilstein:
3587255
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

Quality Level

reaction suitability

reaction type: Grignard Reaction

concentration

1.0 M in diethyl ether

density

0.777 g/mL at 25 °C

SMILES string

C[Si](C)(C)C[Mg]Cl

InChI

1S/C4H11Si.ClH.Mg/c1-5(2,3)4;;/h1H2,2-4H3;1H;/q;;+1/p-1

InChI key

NAQATMJWCJCHOZ-UHFFFAOYSA-M

Looking for similar products? Visit Product Comparison Guide

Application

Reagent used in a variety of nickel catalyzed reactions including alkenation of dithioacetals, cross-coupling with aryl triflates and carbamates, and cross-coupling with vinyl selenides.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3

Target Organs

Central nervous system

Supplementary Hazards

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

-40.0 °F - closed cup

Flash Point(C)

-40 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Accounts of Chemical Research, 24, 257-257 (1991)
Tetrahedron Letters, 35, 6729-6729 (1994)
The Journal of Organic Chemistry, 57, 4066-4066 (1992)

Articles

We carry a large variety of electrophiles and nucleophiles that are widely used in C–C bond-forming reactions. This group of products contains many organometallic reagents as well as commonly-used alkylating and acylating reagents.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service