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3,6,11,14-TETRAMETHOXYDIBENZO[G,P]CHRYSENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60223-52-1

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60223-52-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60223-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,2,2 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60223-52:
(7*6)+(6*0)+(5*2)+(4*2)+(3*3)+(2*5)+(1*2)=81
81 % 10 = 1
So 60223-52-1 is a valid CAS Registry Number.
InChI:InChI=1/C30H24O4/c1-31-17-5-9-21-22-10-6-19(33-3)15-27(22)30-28-16-20(34-4)8-12-24(28)23-11-7-18(32-2)14-26(23)29(30)25(21)13-17/h5-16H,1-4H3

60223-52-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6,11,14-tetramethoxydibenzo[g,p]chrysene

1.2 Other means of identification

Product number -
Other names -

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:60223-52-1 SDS

60223-52-1Downstream Products

60223-52-1Relevant academic research and scientific papers

Dibenzo [g, p] dibenzo [g, p] decen derivative and a new clean clean sensor derivatives

-

Paragraph 0046; 0058-0060; 0063, (2021/11/12)

[Problem] to selectively position the two hydroxyl groups are introduced to clean the sensor 4 [g, p] dibenzo, isomeric products is extremely small, can be made selectively and easily manufacture, and dibenz [g, p] new clean derivative manufactured by the manufacturing method of a sensor. (1) Dibenzo [g, p] [solution] clean sensor brominated, step 4 synthesis of bromide, bromine atoms (2) bromide 4 silylated, silylation process for synthesizing, and, (3) silylation of hydroxy-silyl group by oxidation reaction, synthesis of 2, 7, 10, 15 having a hydroxyl group at step dibenzo [g, p] [g, p] decen tetra- hydroxy dibenzo clean cleaning method for the production of derivatives of the sensor. Also, an oxygen functional group bonded to the dimerization of the fluorenone, 3, 6, 11, 14 and a hydroxyl derivative of [g, p] method for producing clean tetra- hydroxy dibenzo new sensor. [Drawing] no

Regio-defined multi-hydroxylation of Dibenzo[g,p]chrysene

Yoshida, Naoki,Kamiguchi, Shinsuke,Sakao, Kazuki,Akasaka, Ryuhei,Fujii, Yoshino,Maruyama, Tomoyuki,Iwasawa, Tetsuo

supporting information, (2020/05/22)

Regioselective direct tetra-bromination of dibenzo[g,p]chrysene (DBC) is described, involving the synthesis of multi-hydroxyl DBC derivatives. Addition of 16 equiv Br2 to a suspension of DBC in CH2Cl2 enables to singly construct a 2,7,10,15-tetrabromo-DBC. A lithium-bromine exchange event leads the corresponding silyl molecule, and the following oxidation formed a tetra-hydroxyl derivative. Its isomeric tetra-hydroxyl DBC as well as more congested octa-hydroxyl DBC were also singly constructed. These straightforward and simple synthetic routes would provide a general entry for new DBC materials.

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