Di-tert-butyl dicarbonate solution - 2.0M in Toluene

CAS: 24424-99-5

Ref. 3D-FD172651

Produktinformation

• Name: Di-tert-butyl dicarbonate solution - 2.0M in Toluene
• Synonyme: (Boc)2O, (Boc)₂O, Bis(1,1-dimethylethyl) dicarbonate, Bis(tert-butoxycarbonyl) ether, Bis(tert-butyl) dicarbonate, Boc Anhydride, Butyl dicarbonate, Di-tert-, Carbonate de di(tert-butyle), Carbonato De Di(Terc-Butilo), Di(Tert-Butyl) Carbonate, Di(tert-butyl)carbonat, Di-t-butyl-dicarbonate, Di-tert-butyl oxydiformate, Di-tert-butyl pyrocarbonate, Diboc, Dicarbonic acid bis(1,1-dimethylethyl)ester, Dicarbonic acid, 1,3-bis(1,1-dimethylethyl) ester, Dicarbonic acid, C,C'-bis(1,1-dimethylethyl) ester, Formic acid, oxydi-, di-tert-butyl ester, Pyrocarbonic acid di-tert-butyl ester, Tert-Butoxycarbonyl Anhydride, tert-Butoxycarbonyl tert-butyl carbonate, tert-Butoxycarboxylic anhydride, tert-Butyl dicarbonate

Beschreibung

Boc-anhydride is widely used for the introduction of the acid-labile Boc-protecting group in organic synthesis. It is extensively used for the protection of amino groups in the synthesis of amino acids, alkaloids, and peptides. Boc-anhydride reacts rapidly and cleanly with the only by-products being carbon dioxide and t-butanol. It is an efficient tert-butoxycarbonylating agent for alcohols and thiols. This group is easily removed by thermolysis or under moderately acidic conditions, such as, treatment with TFA. The Boc protecting group strategy is the preferred method of choice due to its: easy installation, removal, stability towards nucleophiles, and strong basic conditions. In the presence of moisture, it decomposes into tert-butanol and CO2.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 218.25 g/mol
• Formel: C₁₀H₁₈O₅
• Reinheit: Min. 95%
• InChl: InChI=1S/C10H18O5/c1-9(2,3)14-7(11)13-8(12)15-10(4,5)6/h1-6H3
• InChI Key: InChIKey=DYHSDKLCOJIUFX-UHFFFAOYSA-N
• SMILES: CC(C)(C)OC(=O)OC(=O)OC(C)(C)C