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Benzothieno[2,3-b]pyridine is a heterocyclic compound characterized by the fusion of a benzene ring, a thiophene ring, and a pyridine ring. This unique structure endows it with a range of chemical properties that can be exploited in various applications, such as in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. The compound's molecular formula is C12H7NS, reflecting its composition of carbon, hydrogen, nitrogen, and sulfur atoms. Its chemical structure and properties make it a versatile building block in organic synthesis, particularly in the development of complex molecular architectures with potential biological activity.

244-93-9

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244-93-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 244-93-9 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 244-93:
(5*2)+(4*4)+(3*4)+(2*9)+(1*3)=59
59 % 10 = 9
So 244-93-9 is a valid CAS Registry Number.

244-93-9SDS

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 Benzo[b]thieno[2,3-b]pyridine

1.2 Other means of identification

Product number -
Other names Benzo [b] thieno [2,3-b] 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:244-93-9 SDS

244-93-9Relevant academic research and scientific papers

Facile preparation of benzo[4,5]thieno[2,3-b]pyridines and naphtho[b-4,5]thieno[2,3-b]pyridines via the reaction of Barton esters and benzynes

Rao, U. Narasimha,Biehl, Ed

, p. 3409 - 3411 (2002)

Titled compounds were prepared in a one-pot synthesis by generating symmetrically substituted benzyne intermediates by the diazotization of anthranilic acids in the presence of Barton esters. Unsymmetrically substituted aryne either gave mixtures of regioisomers or failed. However, nitro and methyl derivatives of titled compounds could be obtained as single products using appropriately substituted Barton esters.

Organic compound, and organic light emitting diode and organic light emitting device including the organic compound

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Paragraph 0208; 0213-0216, (2021/05/12)

The present disclosure relates to an organic compound having the following structure, and an organic light emitting diode (OLED) and an organic light emitting device including the organic compound. The organic compound is applied into an emission layer so that the OLED and the organic light emitting device lower their driving voltage, and improves their luminous efficiency and color purity.

Heterocyclic compound, synthetic method thereof and organic light-emitting diode containing compound

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Paragraph 0079; 0085-0086; 0118; 0124-0125, (2019/10/10)

The invention relates to a heterocyclic compound, a synthetic method thereof and an organic light-emitting diode containing the compound. The structural formula of the heterocyclic compound is as shown in the figure I in the specification. According to th

Pyrene derivatives comprising heteroaryl amine groupand organic light-emitting diode including the same

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Paragraph 0369-0374, (2016/10/10)

The present invention relates to a pyrene derivative represented by chemical formula A, and an organic light emitting device including the same. In the chemical formula A, a substituent Z, Ar1 to Ar4, and m are the same as described in the specification.COPYRIGHT KIPO 2016

New entry to benzo[b]thieno[2,3-b]- and benzo[b]thieno-[3,2-b]-pyridines using 2- and 3-azidobenzo[b]thiophene as the nitrogen precursors

Degl'Innocenti, Alessandro,Funicello, Maria,Scafato, Patrizia,Spagnolo, Piero,Zanirato, Paolo

, p. 2561 - 2563 (2007/10/03)

N-(3-Benzo[b]thienyl)- and N-(2-benzo[b]thienyl)-iminotriphenylphosphorane - prepared from the corresponding azidobenzo[b]thiophenes - react with α,β-unsaturated aldehydes under mild conditions to give directly benzo-[b]thieno[3,2-b]- and benzo[b]thieno[2

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