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589284 Aldrich

1-[(Trimethylsilyl)methyl]benzotriazole

99%

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Properties

Related Categories C-C Bond Formation, Chemical Synthesis, Other Synthetic Reagents for C-C Bond Formation, Synthetic Reagents
InChI Key   VRGRHLJMRVGQCS-UHFFFAOYSA-N
assay   99%
mp   56-60 °C(lit.)

Description

Packaging

5 g in glass bottle

Application

New Benzotriazole Reagents

Reactant for:
• Alkylation reactions
• Preparation of inhibitor of p53-MDM2 complex formation

• Used as a one-carbon synthon for one-carbon homologation of carboxylic acids

Price and Availability


Cross-Coupling Guide
Safety & Documentation

Safety Information

Symbol 
GHS07  GHS07
Signal word 
Warning
Hazard statements 
Precautionary statements 
Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
3
Protocols & Articles

Articles

Benzotriazole Reagents

Benzotriazole has been commonly employed as a leaving group and has been used extensively as a novel synthetic auxiliary.  Much of its attractiveness lies in its ability to be introduced readily and ...

Related Content

Benzotriazole Reagents in Chemical Synthesis

Benzotriazole has been commonly employed as a leaving group and has been used extensively as a novel synthetic auxiliary.  Much of its attractiveness lies in its ability to be introduced readily and ...
Keywords: Aldrichimica Acta, Methods

Indoles, Purines, and Their Isosteres

Substituted indoles and purines have frequently been referred to as “privileged structures” since they are capable of binding to multiple receptors with high affinity, and thus have applications acro...
Keywords: Building blocks, Medicinal chemistry

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