14927-65-2 Usage
Bicyclic ketone structure
Six-membered ring fused to a seven-membered ring
The compound has a unique bicyclic structure, with one six-membered ring connected to a seven-membered ring, which contributes to its chemical and structural properties.
Chemical compound classification
Bicyclic ketone
As a bicyclic ketone, it has a carbonyl group (C=O) within its molecular structure, which is responsible for its reactivity and properties.
Fragrance industry use
Sweet, floral, and woody odor
1,2,3,6,7,8-Hexahydroas-Indacen-1-One is valued in the fragrance industry for its pleasant and complex scent, which can be used to create various perfumes and scented products.
Biological activities
Anti-inflammatory and antiproliferative properties
The compound has been found to exhibit potential anti-inflammatory and antiproliferative effects, which could be useful in the development of pharmaceuticals and other treatments.
Potential applications
Pharmaceuticals, agriculture, and materials science
Due to its interesting chemical and structural properties, 1,2,3,6,7,8-Hexahydroas-Indacen-1-One has been studied for its potential use in various fields, including pharmaceuticals, agriculture, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 14927-65-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,2 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14927-65:
(7*1)+(6*4)+(5*9)+(4*2)+(3*7)+(2*6)+(1*5)=122
122 % 10 = 2
So 14927-65-2 is a valid CAS Registry Number.
14927-65-2Relevant articles and documents
DIHYDRO-CYCLOPENTA-ISOQUINOLINE SULFONAMIDES DERIVATIVES
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Page/Page column 26, (2021/07/02)
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
Neudeck, Horst K.
, p. 627 - 658 (2007/10/02)
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
