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1,4,7,10,13,16-Hexaoxacyclooctadecane-2-methanol

Catalog Number ACM70069044-3
CAS 70069-04-4
Structure 1,4,7,10,13,16-Hexaoxacyclooctadecane-2-methanol
Description 1,4,7,10,13,16-Hexaoxacyclooctadecane-2-methanol, also known as HOCM, is an organic compound that plays an important role in a variety of scientific research applications. HOCM is a versatile compound that has been used in a variety of fields, including organic synthesis, biochemistry, and pharmacology. HOCM is a cyclic ether compound with a molecular weight of 254.3 g/mol, and is composed of a hexagonal ring structure with 18 carbon atoms and 16 oxygen atoms.
IUPAC Name 1,4,7,10,13,16-hexaoxacyclooctadec-2-ylmethanol
Molecular Weight 294.34 g/mol
Molecular Formula C13H26O7
Canonical SMILES C1COCCOCCOC(COCCOCCO1)CO
InChI InChI=1S/C13H26O7/c14-11-13-12-19-8-7-17-4-3-15-1-2-16-5-6-18-9-10-20-13/h13-14H,1-12H2
InChI Key HFRGASADQCZXHH-UHFFFAOYSA-N
Application 1,4,7,10,13,16-Hexaoxacyclooctadecane-2-methanol has been used in a variety of scientific research applications, including organic synthesis, biochemistry, and pharmacology. In organic synthesis, 1,4,7,10,13,16-Hexaoxacyclooctadecane-2-methanol is used as a starting material for the synthesis of a variety of organic compounds, such as alcohols, aldehydes, and ketones. In biochemistry, 1,4,7,10,13,16-Hexaoxacyclooctadecane-2-methanol is used as a reagent for the synthesis of peptides, proteins, and other biomolecules. In pharmacology, 1,4,7,10,13,16-Hexaoxacyclooctadecane-2-methanol is used as a starting material for the synthesis of a variety of drugs and pharmaceuticals.
GHS Pictogram Irritant
Properties The biochemical and physiological effects of 1,4,7,10,13,16-Hexaoxacyclooctadecane-2-methanol are not fully understood. However, 1,4,7,10,13,16-Hexaoxacyclooctadecane-2-methanol has been shown to have a variety of effects on enzymes and other proteins, including changes in their structure and function. In addition, 1,4,7,10,13,16-Hexaoxacyclooctadecane-2-methanol has been shown to interact with metal ions, leading to changes in their reactivity and stability.

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