Gelest, Inc. t-BUTYLDIMETHYLCHLOROSILANE, 2.85M in toluene, 48-52% solution SIB1935.5

Description
Additional Properties Hydrolytic Sensitivity 7: reacts slowly with moisture/water Safety Packaging Under Nitrogen Trialkylsilyl Blocking Agent Used as a protecting group for reactive hydrogens in alcohols, amines, thiols, and carboxylic acids. Organosilanes are hydrogen-like, can be introduced in high yield, and can be removed under selective conditions. They are stable over a wide range of reaction conditions and can be removed in the presence of other functional groups, including other protecting groups. The tolerance of silylated alcohols to chemical transformations summary is presented in Table 1 of the Silicon-Based Blocking Agents brochure. tert-Butyldimethylch lorosilane; TBS-Cl; Chlorodimethyl-t-but ylsilane; tert-Butylchlorodime thylsilane; Chloro(1,1-dimethyle thyl)dimethylsilane 2.85M in toluene Used for the protection of alcohols, amines, thiols, lactams, and carboxylic acids Clean NMR characteristics of protecting group Facile removal with flouride ion sources Summary of selective deprotection conditions is provided in Table 7 through Table 20 of the Silicon-Based Blocking Agents brochure
Datasheet
Description
Additional Properties Hydrolytic Sensitivity 7: reacts slowly with moisture/water Safety Packaging Under Nitrogen Trialkylsilyl Blocking Agent Used as a protecting group for reactive hydrogens in alcohols, amines, thiols, and carboxylic acids. Organosilanes are hydrogen-like, can be introduced in high yield, and can be removed under selective conditions. They are stable over a wide range of reaction conditions and can be removed in the presence of other functional groups, including other protecting groups. The tolerance of silylated alcohols to chemical transformations summary is presented in Table 1 of the Silicon-Based Blocking Agents brochure. tert-Butyldimethylch lorosilane; TBS-Cl; Chlorodimethyl-t-but ylsilane; tert-Butylchlorodime thylsilane; Chloro(1,1-dimethyle thyl)dimethylsilane 2.85M in toluene Used for the protection of alcohols, amines, thiols, lactams, and carboxylic acids Clean NMR characteristics of protecting group Facile removal with flouride ion sources Summary of selective deprotection conditions is provided in Table 7 through Table 20 of the Silicon-Based Blocking Agents brochure
Datasheet

Suppliers

Company
Product
Description
Supplier Links
t-BUTYLDIMETHYLCHLOROSILANE, 2.85M in toluene, 48-52% solution - SIB1935.5 - Gelest, Inc.
Morrisville, PA, United States
t-BUTYLDIMETHYLCHLOROSILANE, 2.85M in toluene, 48-52% solution
SIB1935.5
t-BUTYLDIMETHYLCHLOROSILANE, 2.85M in toluene, 48-52% solution SIB1935.5
Additional Properties Hydrolytic Sensitivity 7: reacts slowly with moisture/water Safety Packaging Under Nitrogen Trialkylsilyl Blocking Agent Used as a protecting group for reactive hydrogens in alcohols, amines, thiols, and carboxylic acids. Organosilanes are hydrogen-like, can be introduced in high yield, and can be removed under selective conditions. They are stable over a wide range of reaction conditions and can be removed in the presence of other functional groups, including other protecting groups. The tolerance of silylated alcohols to chemical transformations summary is presented in Table 1 of the Silicon-Based Blocking Agents brochure. tert-Butyldimethylch lorosilane; TBS-Cl; Chlorodimethyl-t-but ylsilane; tert-Butylchlorodime thylsilane; Chloro(1,1-dimethyle thyl)dimethylsilane 2.85M in toluene Used for the protection of alcohols, amines, thiols, lactams, and carboxylic acids Clean NMR characteristics of protecting group Facile removal with flouride ion sources Summary of selective deprotection conditions is provided in Table 7 through Table 20 of the Silicon-Based Blocking Agents brochure

Additional Properties


  • Hydrolytic Sensitivity 7: reacts slowly with moisture/water
    Safety
  • Packaging Under Nitrogen
    Trialkylsilyl Blocking Agent
    Used as a protecting group for reactive hydrogens in alcohols, amines, thiols, and carboxylic acids. Organosilanes are hydrogen-like, can be introduced in high yield, and can be removed under selective conditions. They are stable over a wide range of reaction conditions and can be removed in the presence of other functional groups, including other protecting groups. The tolerance of silylated alcohols to chemical transformations summary is presented in Table 1 of the Silicon-Based Blocking Agents brochure.
    tert-Butyldimethylchlorosilane; TBS-Cl; Chlorodimethyl-t-butylsilane; tert-Butylchlorodimethylsilane; Chloro(1,1-dimethylethyl)dimethylsilane
  • 2.85M in toluene
  • Used for the protection of alcohols, amines, thiols, lactams, and carboxylic acids
  • Clean NMR characteristics of protecting group
  • Facile removal with flouride ion sources
  • Summary of selective deprotection conditions is provided in Table 7 through Table 20 of the Silicon-Based Blocking Agents brochure
Supplier's Site Datasheet

Technical Specifications

  Gelest, Inc.
Product Category Organic Chemicals
Product Number SIB1935.5
Product Name t-BUTYLDIMETHYLCHLOROSILANE, 2.85M in toluene, 48-52% solution
Chemical Formula C 6 H 1 5 ClSi
Unlock Full Specs
to access all available technical data

Similar Products

Intermediates and Ingredients for Pharmaceuticals and Agrochemical Compounds -  - AGC Chemicals Americas, Inc.
Specs
Chemical Family All Halogenated
Chemical Name Trifluoroacetic Acid, Trifluoroacetic Anhydride, Ethyl Trifluoroacetate, Sodium Trifluoroacetate, 2,3,4-Trifluoro aniline, Trifluoroacetamide, & More
CAS Number 76-05-1, 407-25-0, 383-63-1, 2923-18-4, 3862-73-5, 354-38-1, 148043-73-6, 30071-93-3, 677-69-0, 122665-97-8, 118612-00-3, 136040-19-2, and More
View Details
DMI 1,3 Dimethyl-2-Imidazolidinone -  - Mitsui Chemicals America, Inc.
Mitsui Chemicals America, Inc.
Specs
Trigger Solvent
Chemical Name DMI 1,3 Dimethyl-2-Imidazolidinone
State of Matter Liquid / Solution
View Details
A.G. Scientific, Inc.
Specs
Trigger Salt
Chemical Formula C12H6N4O6S. 2Na
CAS Number 118876-58-7 (for non salt form)
View Details
TITRATION SOLVENT - LC261404 - LabChem Inc.
Specs
Trigger Solvent
View Details