Detail of "13380-94-4"

CAS Number:
13380-94-4
Name:
4,7-Methano-5H-inden-5-one,octahydro-
Molecular Structure:
Formula:
C10H14 O
Molecular Weight:
150.24
Synonyms:
4,7-Methanoindan-5(4H)-one,tetrahydro- (6CI,7CI,8CI); 8-Ketotricyclo[5.2.1.02,6]decane;8-Oxotricyclo[5.2.1.02,6]decane; NSC 77098; Tricyclo[5.2.1.02,6]decan-8-one
Density:
1.105 g/cm³
Boiling Point:
234.9ºC at 760 mmHg
Flash Point:
101.1 ºC
Safety:
Moderately toxic by ingestion and skin contact. When heated to decomposition it emits acrid smoke and irritating fumes. Details

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Soothing cosmetic lotions: Soothing cosmetic lotions. (Kao Corp., Japan). Jpn. 96297-56-2 which is the cas registry number is also used here. Kokai Tokkyo Koho JP 59219208 A2 10 Dec 1984 Showa, 8 pp. (Japanese). (Japan). CODEN: JKXXAF. CLASS: ICM: A61K007-00. ICS: A23L001-00; A61K007-32; A61K047-00. ICA: A23G003-00; A23L002-00. APPLICATION: JP 83-93454 27 May 1983. DOCUMENT TYPE: Patent CA Section: 62 (Essential Oils and Cosmetics) Section cross-reference(s): 24 Soothing cosmetic lotions contain tricyclic alcs. I (R = C1-8 alkyl). Thus, a lotion comprises 8-ethyltricyclo[5.2.1.02,6]decan-8-ol (II) [96297-56-2] 1.0 and EtOH 99.0% by wt. II was prepd. by treating tricyclo[5.In this experiment, several chemicals are used like 96297-56-2 2.1.02,6]decan-8-one [13380-94-4] in Et2O with EtI in the presence of Mg. ..

Derivatives of dicyclopentadiene in ground water: Derivatives of dicyclopentadiene in ground water. Van Breemen, Richard B.; Fenselau, Catherine C.; Cotter, Robert J.; Curtis, Allan J.; Connolly, Gaydie (Sch. Med., Johns Hpkins Univ., Baltimore 21205, USA). Biomed. Environ.Some commonly used reagents like 77-73-6 and 13380-94-4 are used in this experiment. Mass Spectrom., 14(3), 97-102 (English) 1987. CODEN: BEMSEN. ISSN: 0887-6134. DOCUMENT TYPE: Journal CA Section: 61 (Water) Section cross-reference(s): 60 Dicyclopentadiene (I) [77-73-6], a waste product of manufg. at the Rocky Mountain Arsenal near Denver, Colorado, was detd. in groundwater by gas chromatog.-mass spectrometry (GC/MS), and derivs. of I were present in addn. to I and other chem. wastes. The derivs. thus identified were characterized by GC high resoln. MS, D exchange for active H in the chem. ionization source of the mass spectrometer, and GC/MS following on-column base catalyzed deuteration of enolizable H. Two ketone derivs. of I were identified by comparison with synthetic stds. Groundwater derivs. of I were compared with mammalian enzymic metabolites produced in vitro by incubation with immobilized rabbit liver cytochromes P-450. The metabolites were analyzed by GC/MS and by GC/MS following derivatization and D labeling. Although not found in groundwater samples, the two metabolites were identified as monoepoxides of I by comparison with compds. synthesized in the lab. .