t-Butyl Magnesium Chloride Series

CAS Number: 677-22-5

Molecular Formula: C4H9ClMg

Purity: t-Butyl Magnesium Chloride Series 95% purity

About t-Butyl Magnesium Chloride Series

t-Butylmagnesium chloride (CAS 677-22-5) is a cornerstone of the API intermediates market, serving as a highly effective Grignard reagent for the sterically hindered introduction of the tert-butyl group in complex pharmaceutical syntheses (Pharma purity 99%). Chloro(1,1-dimethylethyl)magnesium has seen a surge in deman...

Variants

tert-Butylmagnesium chloride

CAS: 677-22-5

t-Butyl Magnesium Chloride Series Specifications

CAS Number

677-22-5

Molecular Formula

C4H9ClMg

Molecular Weight

116.87 g/mol

IUPAC Name

magnesium;2-methylpropane;chloride

Canonical SMILES

CC(C)(C)[Mg]Cl

InChI Key

ZDRJSYVHDMFHSC-UHFFFAOYSA-M

CAS Number

677-22-5

Molecular Formula

C4H9ClMg

Molecular Weight

116.87 g/mol

IUPAC Name

magnesium;2-methylpropane;chloride

Canonical SMILES

CC(C)(C)[Mg]Cl

InChI Key

ZDRJSYVHDMFHSC-UHFFFAOYSA-M

Molecular Weight

116.87 g/mol

Purity

t-Butyl Magnesium Chloride Series 95% purity

Boiling Point

ca. 34.7 °C at 1,013 hPa (Diethyl ether)

Freezing point

-108°C (Tetrahydrofuran)

Grignard Reagent

A powerful carbon nucleophile and organometallic compound primarily used for C-C bond formation in the synthesis of complex organic molecules and pharmaceuticals

Pharmaceutical Intermediate

A critical building block utilized in the synthesis of various medicinal compounds, active pharmaceutical ingredients (APIs), and new allylamine antifungal drugs

Organic Synthesis Building Block

A versatile reagent employed for the introduction of the bulky tert-butyl group into organic molecules via nucleophilic addition or cross-coupling reactions

Chemical Base

A strong, weakly nucleophilic base used in deprotonation reactions within academic and industrial research

Fine Chemical Intermediate

A high-purity reagent used in metalation and Grignard metathesis reactions for the production of specialized chemicals and polymers like polyhexylthiophenes.