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Benzothiazole, 2-(2-furanyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1569-98-8 Structure
  • Basic information

    1. Product Name: Benzothiazole, 2-(2-furanyl)- (9CI)
    2. Synonyms: Benzothiazole, 2-(2-furanyl)- (9CI);2-Furan-2-yl-benzothiazole;2-(2-furyl)-1,3-benzothiazole;2-furan-2-yl-1,3-benzothiazole
    3. CAS NO:1569-98-8
    4. Molecular Formula: C11H7NOS
    5. Molecular Weight: 201.24438
    6. EINECS: N/A
    7. Product Categories: BENZOTHIAZOLE
    8. Mol File: 1569-98-8.mol
  • Chemical Properties

    1. Melting Point: 105 °C
    2. Boiling Point: 336.8 °C at 760 mmHg
    3. Flash Point: 157.5 °C
    4. Appearance: /
    5. Density: 1.303 g/cm3
    6. Vapor Pressure: 0.000214mmHg at 25°C
    7. Refractive Index: 1.667
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 0.85±0.10(Predicted)
    11. CAS DataBase Reference: Benzothiazole, 2-(2-furanyl)- (9CI)(CAS DataBase Reference)
    12. NIST Chemistry Reference: Benzothiazole, 2-(2-furanyl)- (9CI)(1569-98-8)
    13. EPA Substance Registry System: Benzothiazole, 2-(2-furanyl)- (9CI)(1569-98-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1569-98-8(Hazardous Substances Data)

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

1,3-dibromo-5,5-dimethylhydantoin catalyzed one-pot synthesis of 2-arylbenzothiazoles

Yang, Xiaojuan,Liang, Jinying

, p. 1909 - 1915 (2011)

A one-pot synthesis of 2-arylbenzothiazoles from the reaction of 2-aminothiophenol and aromatic aldehydes catalyzed by 1,3-dibromo-5,5- dimethylhydantoin is reported.

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

New synthesis method of 2-arylbenzothiazoles transfer of active electrons by microwave

Ben-Alloum, Abdelkrim,Bakkas, Salem,Soufiaoui, Mohamed

, p. 6395 - 6396 (1997)

The condensation of several aldehydes wtih 2-aminothiophenol on silica gel/nitrobenzene or montmorillonite K10/nitrobenzene under microwave irradiation afforded 2-arylbenzothiazoles in good yields and high purity.

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

A simple iodine-promoted synthesis of 2-substituted benzothiazoles by condensation of aldehydes with 2-aminothiophenol

Li, Yan,Wang, Yu-Lu,Wang, Jin-Ye

, p. 460 - 461 (2006)

Iodine is used to promote the condensation of 2-aminothiophenol with aldehydes in DMF, which affords corresponding 2-substituted benzothiazoles efficiently. Mild and manipulable procedure, use of available and less toxic oxidant, and shorter reaction times are the advantageous features of this method. Copyright

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

A simple and efficient synthesis of (hetero)aryl-substituted benzothiazolyl or benzoxazolyl furan, thiophene and N -methylpyrrole derivatives through a palladium-catalyzed regioselective C-H bond arylation

Abdellaoui, Fatma,Youssef, Chiraz,Ben Ammar, Hamed,Soul, Jean-Franois,Doucet, Henri

, p. 3341 - 3350 (2014)

The synthesis of 2-(hetero)aryl-5-benzothiazol-2-yl or -benzoxazol-2-ylfuran, -thiophene, and -1-methylpyrrole derivatives was accomplished in two steps. 2-(Benzothiazol-2-yl)- or 2-benzoxazol-2-ylfuran, -thiophene, or -1-methylpyrrole were synthesized by

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

Solvent-free synthesis of 2-aryl and 2-alkylbenzothiazoles on silica gel under microwave irradiation

Kodomari, Mitsuo,Tamaru, Yoshimi,Aoyama, Tadashi

, p. 3029 - 3036 (2004)

2-Substituted benzothiazoles have been synthesized by the condensation of o-aminothiophenol and aromatic or aliphatic aldehydes in the presence of silica gel under microwave irradiation (MW) and solvent-free conditions. The silica gel can be easily recovered and reused for subsequent reactions without loss of the activity.

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