CAS 14812-59-0 2-Chloro-4,4,5,5-tetramethyl-1,3,2-dioxaphospholane

Synonyms

AKOS015915850; FT-0739179; 14812-59-0; 2-Chloro-4,4,5,5-tetramethyl-1,3,2-dioxaphospholane, 95%; DTXSID80404385; SCHEMBL1818442; 1,3,2-Dioxaphospholane, 2-chloro-4,4,5,5-tetramethyl-; DB-023477; I14-53007; TC-170771;

IUPAC Name

2-chloro-4,4,5,5-tetramethyl-1,3,2-dioxaphospholane;

Molecular Weight

182.584g/mol

Molecular Formula

C6H12ClO2P;

Canonical SMILES

CC1(C(OP(O1)Cl)(C)C)C;

InChI

InChI=1S/C6H12ClO2P/c1-5(2)6(3,4)9-10(7)8-5/h1-4H3;

InChI Key

WGPCXYWWBFBNSS-UHFFFAOYSA-N;

Complexity

131

Covalently-Bonded Unit Count

Exact Mass

182.026g/mol

H-Bond Acceptor

Heavy Atom Count

Monoisotopic Mass

182.026g/mol

Topological Polar Surface Area

18.5A^2

Application

2-Chloro-4,4,5,5-tetramethyl-1,3,2-dioxaphospholane is an essential solid-state organic reagent predominantly used in chemical and experimental research. Its primary purpose is to facilitate the phosphorylation of alcohols and heteroatoms, thereby enabling the creation of valuable glycosyl donors and ligands. It also plays a crucial role in analytical studies, particularly in the derivatization of lignin samples for 31P NMR analysis. Additionally, this compound serves as a catalyst in CuO/TiO2 catalyzed lignin oxidation research. Known for its reliable performance in various applications, it has specific storage requirements, including maintaining a temperature between 10°C and 25°C, keeping it dry, and storing it under inert nitrogen gas to preserve its efficacy.

February 26, 2025

Essential Tool for Phosphorylation in Research

2-Chloro-4,4,5,5-tetramethyl-1,3,2-dioxaphospholane excels in alcohol phosphorylation for glycosyl donor formation. It's pivotal in lignin oxidation studies, providing consistent results. Highly recommended for seamless integration in experimental research.