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5472-84-4

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5472-84-4 Usage

Chemical Properties

YELLOW-GREEN POWDER

Check Digit Verification of cas no

The CAS Registry Mumber 5472-84-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,7 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5472-84:
(6*5)+(5*4)+(4*7)+(3*2)+(2*8)+(1*4)=104
104 % 10 = 4
So 5472-84-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H8O2/c14-11-7-12(15)10-6-2-4-8-3-1-5-9(11)13(8)10/h1-7,14H

5472-84-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxyphenalen-1-one

1.2 Other means of identification

Product number -
Other names 4-hydroxy-1H-phenalen-1-one

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:5472-84-4 SDS

5472-84-4Relevant articles and documents

Convenient synthesis of 7H-Naphtho-[1,8-gh]quinolin-7-one

Sawada, Tadanobu,Ishii, Hiroyuki,Aoyama, Yoshitomo,Ueda, Toyotoshi,Aoki, Junji,Takekawa, Minoru

, p. 784 - 793 (2012)

7H-Naphtho[1,8-gh]quinolin-7-one was prepared by the glycerol condensation of 3-aminophenalenone in good yields. This method provides a new and convenient synthesis of the compound. NMR spectra of its related compounds were measured, and the rapid interchange between two equivalent a-enone structures was found, which is well known as the phenomenon for the formation of carboxylic acid dimer or hydrogen difluoride ion. Taylor & Francis Group, LLC.

Synthesis of Positional Isomeric Phenylphenalenones

Ospina, Felipe,Ramirez, Adrian,Cano, Marisol,Hidalgo, William,Schneider, Bernd,Otálvaro, Felipe

, p. 3873 - 3879 (2017/04/11)

A series of isomeric phenylphenalenones in which the phenyl ring is located at all possible peripheral positions of the phenalenone nuclei was synthesized. The structural characteristics of the series, in which topological variation is permitted with minimal electronic disturbance, could, in principle, allow for easy pharmacophore recognition when the compounds are aligned in steroidomimetic conformations.

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