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Benzo[b]phenanthro[3,2-d]thiophene is a heterocyclic aromatic compound consisting of a benzene ring fused to a phenanthrene ring, with a sulfur atom replacing one of the carbon atoms in the phenanthrene ring. This unique structure classifies it as a member of the phenanthrothiophene family, which is known for its diverse range of applications in various fields. The compound exhibits interesting electronic and optical properties, making it a potential candidate for use in organic electronics, such as organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs). Additionally, benzo[b]phenanthro[3,2-d]thiophene has been studied for its potential applications in the development of new materials for solar cells and other optoelectronic devices due to its ability to absorb light and transport charge. Its chemical structure also makes it a subject of interest in the synthesis of various pharmaceuticals and agrochemicals, as it can be a key building block in the creation of complex molecular architectures.

241-32-7

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241-32-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 241-32-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,4 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 241-32:
(5*2)+(4*4)+(3*1)+(2*3)+(1*2)=37
37 % 10 = 7
So 241-32-7 is a valid CAS Registry Number.

241-32-7SDS

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 Benzo[b]phenanthro[3,2-d]thiophene

1.2 Other means of identification

Product number -
Other names 2,3,5,6-Dibenzo-thiophanthren

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:241-32-7 SDS

241-32-7Relevant academic research and scientific papers

Thiophene analogues of carcinogenic polycyclic hydrocarbons. Elbs pyrolysis of various aroylmethylbenzo[b]thiophenes

Croisy,Mispelter,Lhoste,et al.

, p. 353 - 359 (2007/10/02)

The synthesis of two benzonaphthothiophenes and of four benzophenanthrothiophenes through Elbs cyclodehydration of ortho-methylated aroylbenzo[b]thiophenes is described. The occurrence of a rearrangement of the thiophene ring in the course of the cyclization is discussed as well as the influence of the temperature on a concurrent cyclodehydration process. Several of these poly-condensed thiophenes were found to be carcinogenic in mice.

The Synthesis of Benzophenathrothiophenes and Anthrabenzothiophenes

Tedjamulia, Marvin L.,Tominaga, Yoshinori,Castle, Raymond N.,Lee, Milton L.

, p. 861 - 866 (2007/10/02)

The synthesis of benzophenanthrothiophene (5), benzophenanthrothiophene (6), benzophenanthrothiophene (9), benzophenanthrothiophene (14a), anthrabenzothiophene (24), anthrabenzothiophene (29) and anthrabenzothiophene (30) is described as well as the preparation of 13-methylbenzophenanthrothiophene (14b).

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