14927-65-2

Basic information

• Product Name: 1,2,3,6,7,8-Hexahydroas-Indacen-1-One
• Synonyms: 1,2,3,6,7,8-Hexahydroas-Indacen-1-One;1,2,3,6,7,8-Hexahydroas-Indacen-1-One(WXC03723)
• CAS NO: 14927-65-2
• Molecular Formula: C12H12O
• Molecular Weight: 172.22308
• Mol File: 14927-65-2.mol
• Article Data: 4

Chemical Properties

• Melting Point: 89-90 °C
• Boiling Point: 323.8±42.0 °C(Predicted)
• Appearance: /
• Density: 1.195±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1,2,3,6,7,8-Hexahydroas-Indacen-1-One(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3,6,7,8-Hexahydroas-Indacen-1-One(14927-65-2)
• EPA Substance Registry System: 1,2,3,6,7,8-Hexahydroas-Indacen-1-One(14927-65-2)

Safety Data

• Hazardous Substances Data: 14927-65-2(Hazardous Substances Data)

Usage

General Description

1,2,3,6,7,8-Hexahydroas-Indacen-1-One, also known as dihydroheliocarpan, is a chemical compound with the molecular formula C13H16O. It is a bicyclic ketone with a six-membered ring fused to a seven-membered ring. 1,2,3,6,7,8-Hexahydroas-Indacen-1-One is commonly used in the fragrance industry for its sweet, floral, and woody odor. It is also known for its potential biological activities, including anti-inflammatory and antiproliferative properties. Additionally, 1,2,3,6,7,8-Hexahydroas-Indacen-1-One has been studied for its potential applications in pharmaceuticals, agriculture, and materials science due to its interesting chemical and structural properties.

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Relevant articles and documents

DIHYDRO-CYCLOPENTA-ISOQUINOLINE SULFONAMIDES DERIVATIVES

The present invention relates to dihydro‐cyclopenta‐isoquinoline derivatives of formula (I): processes for preparing them, pharmaceutical compositions containing them and their use in treating disorders caused by IgE (such as allergic responses, non‐allergic mast cell responses or certain autoimmune responses), and in particular, disorders caused by the interaction of IgE with the FcεRI receptor.

Aromatic Spiranes, XIV: Syntheses of 2,2'-Spirobi-(s-hydrindacene) and its precursors

The title compound 35 was prepared by catalytic reduction of the diones 29a and 11a. 29a was synthesized by systematic anellation of fivemembered rings to the positions 5,6 and 5',6', resp., of 2,2'-spirobiindane.The preparation of 11a was achieved by Friedel-Crafts cyclisation of bis-(5-indanylmethyl)-malonic acid. s-Hydrindacene-1-one 5a was prepared as a precursor for the synthesis of 11a (see forthcoming publication) and its derivates as models for corresponding anellation and substitution reactions. - Keywords: s-Hydrindacene-1-one and derivates; Mono- and bisanellation; 2,2'-Spirobiindane; 1H-nmr spectra