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Benzothieno[2,3-c]pyridine is a heterocyclic compound characterized by the fusion of a benzene ring, a thiophene ring, and a pyridine ring. This complex structure is known for its potential applications in various fields, including pharmaceuticals and materials science, due to its unique electronic and steric properties. The compound's chemical formula is C12H7NS, reflecting its composition of carbon, hydrogen, nitrogen, and sulfur atoms. It is often synthesized through multi-step organic reactions and can be further functionalized to create derivatives with specific properties. The compound's structure and reactivity make it a subject of interest for researchers exploring new compounds with potential therapeutic or technological applications.

244-90-6

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244-90-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 244-90-6 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 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 244-90:
(5*2)+(4*4)+(3*4)+(2*9)+(1*0)=56
56 % 10 = 6
So 244-90-6 is a valid CAS Registry Number.

244-90-6SDS

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 1-benzothieno[2,3-c]pyridine

1.2 Other means of identification

Product number -
Other names Benzo[b]thieno[2,3-c]pyridin

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:244-90-6 SDS

244-90-6Downstream Products

244-90-6Relevant academic research and scientific papers

Cyclization of 2-Biphenylthiols to Dibenzothiophenes under PdCl2/DMSO Catalysis

Zhang, Tao,Deng, Guigang,Li, Hanjie,Liu, Bingxin,Tan, Qitao,Xu, Bin

, p. 5439 - 5443 (2018/09/13)

A palladium-catalyzed synthesis of dibenzothiophenes from 2-biphenylthiols is described. This highly efficient reaction employs a simple PdCl2/DMSO catalytic system, in which PdCl2 is the sole metal catalyst and DMSO functions as an oxidant and solvent. This transformation has broad substrate scope and operational simplicity and proceeds in high yield. The synthetic utility was demonstrated by the facile synthesis of helical dinapthothiophene 3 and an eminent organic semiconductor DBTDT 4. Importantly, highly strained trithiasumanene 5, a buckybowl of considerable synthetic challenge, was observed under this catalytic system.

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