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Phenanthro[3,2-b]thiophene is a heterocyclic aromatic compound consisting of a phenanthrene ring fused with a thiophene ring. It is characterized by the presence of a sulfur atom in the thiophene ring, which imparts unique electronic and chemical properties to the molecule. Phenanthro[3,2-b]thiophene is of interest in the field of organic chemistry and materials science due to its potential applications in the development of novel electronic materials, such as organic semiconductors and optoelectronic devices. The specific arrangement of atoms in phenanthro[3,2-b]thiophene contributes to its distinct chemical reactivity and electronic structure, making it a subject of ongoing research for its potential use in advanced technologies.

224-10-2

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224-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 224-10-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,2 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 224-10:
(5*2)+(4*2)+(3*4)+(2*1)+(1*0)=32
32 % 10 = 2
So 224-10-2 is a valid CAS Registry Number.
InChI:InChI=1/C16H10S/c1-2-4-14-11(3-1)5-6-12-9-13-7-8-17-16(13)10-15(12)14/h1-10H

224-10-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name naphtho[2,1-f][1]benzothiole

1.2 Other means of identification

Product number -
Other names Phenanthro(3,2-b)thiophene

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:224-10-2 SDS

224-10-2Relevant academic research and scientific papers

Cascade reaction for the synthesis of polycyclic aromatic hydrocarbons via transient directing group strategy

Wang, Ziqi,Dong, Wendan,Sun, Bing,Yu, Qinqin,Zhang, Fang-Lin

supporting information, p. 4031 - 4041 (2019/07/03)

A Pd(II)-catalyzed cascade synthesis of diverse polycyclic aromatic hydrocarbons via transient directing group strategy has been developed, involving the consecutive arylation, cyclization and aromatization. The efficiency and practicality were demonstrated by wide substrate range, concise synthetic pathway and mild reaction conditions. The subsequent transformations of the benz[a]anthracene core accessed natural bioactive PAH molecules.

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