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1569-98-8

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1569-98-8 Usage

Synthesis Reference(s)

Chemical and Pharmaceutical Bulletin, 18, p. 587, 1970 DOI: 10.1248/cpb.18.587

Check Digit Verification of cas no

The CAS Registry Mumber 1569-98-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,6 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1569-98:
(6*1)+(5*5)+(4*6)+(3*9)+(2*9)+(1*8)=108
108 % 10 = 8
So 1569-98-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H7NOS/c1-2-6-10-8(4-1)12-11(14-10)9-5-3-7-13-9/h1-7H

1569-98-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(furan-2-yl)-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names 2-furan-2-yl-benzothiazole

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:1569-98-8 SDS

1569-98-8Relevant articles and documents

A simple, microwave-assisted, and solvent-free synthesis of 2-arylbenzothiazoles by acetic acid-promoted condensation of aldehydes with 2-aminothiophenol in air

Azarifar, Davood,Maleki, Behrooz,Setayeshnazar, Mehrnaz

, p. 2097 - 2102 (2009)

An efficient and simple procedure has been developed for the synthesis of various 2-arylbenzothiazoles by acetic acid-promoted condensation of 2 -aminothiophenol with aromatic aldehydes under microwave irradiation and solvent-free conditions in high yield

Sulfonated porous Carbon (SPC)-catalyzed synthesis of benzothiazole derivatives in water

Shokrolahi, Arash,Zali, Abbas,Mahdavi, Mohammd

, p. 535 - 543 (2012)

A simple and efficient procedure has been developed for the synthesis of benzothiazole derivatives in water by the condensation of 2-aminothiophenol with aldehydes in the presence of Sulfonated porous carbon (SPC). This method provides a simple and effici

An efficient green synthesis of 2-arylbenzothiazole analogues as potent antibacterial and anticancer agents

Chhabra, Mohit,Sinha, Sohini,Banerjee, Swagata,Paira, Priyankar

, p. 213 - 217 (2016)

We have demonstrated a novel and green approach for the synthesis of 2-substituted benzothiazole analogues. A number of 2-aryl and heteroaryl benzothiazole scaffolds were synthesized using Amberlite IR-120 resin under microwave irradiation. The catalytic

ZnO-beta zeolite: As an effective and eco-friendly heterogeneous catalyst for the synthesis of benzothiazole derivatives

Katkar, Santosh S.,Mohite, Pravinkumar H.,Gadekar, Lakshman S.,Vidhate, Kaluram N.,Lande, Machhindra K.

, p. 421 - 425 (2010)

A cheap and recyclable ZnO-beta zeolite was used as catalyst for the synthesis of benzothiazole derivatives. This method provides several advantages such as environmental friendliness, short reaction times, high yields, simple work-up procedure and cataly

Synthesis of 2-arylbenzimidazoles and 2-arylbenzothiazoles in both room temperature and microwave condition catalyzed by hexamethylenetetramine-bromine complex

Khosravi, Kaveh,Kazemi, Samira

, p. 61 - 64 (2012)

One-pot condensation of 2-aminothiophenol or 1,2-phenylenediamine with different aldehydes has been catalyzed by hexamethylenetetramine-bromine (HMTA-Bromine) as new, available and effective catalyst. 2-Arylbenzo-thiazoles and 2-aryl-benzimidazoles have b

P2O5 mediated rapid condensation of 2-aminothiophenol with aromatic aldehydes at ambient temperature

Nalage, Santosh V.,Bhosale, Sidhanath V.,Bhosale, Dattatry S.,Jadhav, Wamanrao N.

, p. 790 - 793 (2010)

2-Arylbenzothiazoles formed in good yields (65-90%) by the condensation of aminothiophenols with aromatic aldehydes using P2O5 at ambient temperature.

Ultrasound-assisted efficient and green synthesis of 2-substituted benzothiazoles under solvent-free condition using recyclable sulfated tungstate

Pise, Ashok S.,Ingale, Ajit P.,Dalvi, Navnath R.

supporting information, p. 3629 - 3641 (2021/10/12)

Sulfated tungstate catalyzed an efficient and ecofriendly protocol has been described for the synthesis of 2-substituted benzothiazoles. The corresponding benzothiazoles were obtained using a condensation reaction of 2-aminothiophenol with various aldehydes under ultrasound irradiation at room temperature. Various functional groups on the 2-aminothiophenol as well as on the aldehydes were tolerated to provide 2-substituted benzothiazoles derivatives in excellent yields. The faster reaction rate, solvent-free or mild reaction conditions, wide functional group compatibility, excellent yields, easy work-up procedure, and excellent catalyst recyclability are the advantages of this protocol. These advantages make this process more practicable, cost-effective, and environmentally benign.

Pentafluorophenylammonium Triflate: A Mild, Efficient and Reusable Catalyst for the Synthesis of 2-Arylbenzothiazole and 2-Arylbenzothiazoline Derivatives in a Green Chemical Approach

Datta, Arup

, p. 95 - 102 (2021/03/29)

In this work, one pot, simple and environmentally benign effective synthesis of 2-substituted benzothiazole and benzothiazoline derivatives are described in presence of PFPAT (pentafluorophenylammonium triflate) catalyst in water successfully. A series of benzothiazole derivative were synthesized by the reaction between 2-aminothiophenol and various aldehydes in good yields. Recyclability of the catalyst is observed for four times without loss of its activity in aqueous medium.

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