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573-22-8

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573-22-8 Usage

Description

3,4-Dihydro-2H-phenanthren-1-one, also known as Dibenzo[a,e]cyclooctene-5,7-dione, is a chemical compound belonging to the phenanthrene class with the molecular formula C14H10O. It is a dihydrophenanthrene derivative featuring a ketone functional group. Although not widely studied or commonly used in industry or research, this compound holds potential interest for chemists and researchers in the field of phenanthrene compounds.

Uses

Given the limited information on 3,4-Dihydro-2H-phenanthren-1-one, its applications are currently not well-documented. However, based on its chemical structure and the properties of similar compounds, potential uses may include:
Used in Chemical Research:
3,4-Dihydro-2H-phenanthren-1-one is used as a research compound for [application reason], such as studying the properties and reactions of phenanthrene derivatives, which could contribute to the development of new chemical processes or materials.
Used in Pharmaceutical Development:
3,4-Dihydro-2H-phenanthren-1-one may be used as a starting material or intermediate in the synthesis of pharmaceutical compounds, given its unique structure and the presence of a ketone functional group, which can be further modified for medicinal chemistry applications.
Used in Material Science:
3,4-Dihydro-2H-phenanthren-1-one could potentially be used in the development of new materials, such as organic semiconductors or polymers, due to its aromatic and conjugated structure, which may exhibit interesting electronic or optical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 573-22-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,7 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 573-22:
(5*5)+(4*7)+(3*3)+(2*2)+(1*2)=68
68 % 10 = 8
So 573-22-8 is a valid CAS Registry Number.
InChI:InChI=1/C14H12O/c15-14-7-3-6-12-11-5-2-1-4-10(11)8-9-13(12)14/h1-2,4-5,8-9H,3,6-7H2

573-22-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-Dihydro-2H-phenanthren-1-one

1.2 Other means of identification

Product number -
Other names 1-keto-1,2,3,4-tetrahydrophenanthrene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:573-22-8 SDS

573-22-8Relevant articles and documents

Photolyses of (3-Naphthoxypropyl)-, (4-Naphthylbutyl)-, and (4-Naphthyl-4-oxobutyl)cobaloxime

Tada, Masaru,Hiratsuka, Mitsunori,Goto, Hiroyuki

, p. 4364 - 4370 (2007/10/02)

The cobalt-carbon bond of the titled compounds is photochemically cleaved to generate an organoradical and a cobaloxime(II) radical pair. 3-(1- or 2-naphtoxy)propyl, 4-(1- or 2-naphthyl)butyl, and 4-(1-or 2-napthyl)-4-oxobutyl radicals thus formed undergo three types of reactions: (a) hydrogen abstraction to give a saturated terminal, (b) hydrogen elimination to give a terminal olefin, and (c) substitution on the naphthalene ring.In benzene and radicals follow process b exclusively (the radicals from (3-(2-napthoxy)propyl)cobaloxime (1a), (3-(1-napthoxy)propyl)cobaloxime (2a), and (4-(1-napthyl)butyl)cobaloxime (2 b)) or preferentially (the radicals from (4-(2-napthyl)butyl)cobaloxime (1 b), (4-(2-napthyl)-4-oxobutyl)cobaloxime (1c), and 4-(1-napthyl)-4-oxobutyl)cobaloxime (2c)).In chloroform, process a becomes important to the extent as the sum of the other two processes.In water-acetonitril (4:1), process c becomes important and even takes precedence of others for the radicals from 1b and 1c.This feature is accounted for by the folding of the side chain of hydrophobic radicals.Encapsulation of the radicals in β-cyclodextrin stimulates process c except for the case of the radical from 2c.In the case of cobaloxime 2c, α-cyclodextrin does not effect the partition process of the intermediate radical.This feature is accounted for by the shallow inclusion of the radical due to the hydrogen bonding as depicted in Figure 1d.

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