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2-phenylthiochroman is a chemical compound with the molecular formula C15H13OS. It is a derivative of the chroman ring system, which is a heterocyclic compound consisting of a benzene ring fused to a pyran ring. The "2-phenyl" part of its name indicates that there is a phenyl group (a benzene ring) attached to the second carbon of the chroman ring. The "thio" in its name signifies the presence of a sulfur atom in the molecule, which is part of a thiophene ring fused to the chroman. 2-phenylthiochroman is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and properties. It is an example of how the fusion of different ring systems can lead to the creation of complex and potentially useful molecules in the field of organic chemistry.

5961-99-9

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5961-99-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5961-99-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,6 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5961-99:
(6*5)+(5*9)+(4*6)+(3*1)+(2*9)+(1*9)=129
129 % 10 = 9
So 5961-99-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H14S/c1-2-6-12(7-3-1)15-11-10-13-8-4-5-9-14(13)16-15/h1-9,15H,10-11H2

5961-99-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-3,4-dihydro-2H-thiochromene

1.2 Other means of identification

Product number -
Other names NRYGFMAOIPXXBW-UHFFFAOYSA

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:5961-99-9 SDS

5961-99-9Downstream Products

5961-99-9Relevant academic research and scientific papers

Copper-Catalyzed Domino Synthesis of 2-Arylthiochromanones through Concomitant C-S Bond Formations Using Xanthate as Sulfur Source

Sangeetha, Subramani,Muthupandi, Pandi,Sekar, Govindasamy

, p. 6006 - 6009 (2016/01/09)

An efficient domino process for the synthesis of thioflavanones has been described using a copper catalyst without addition of any external ligand. A variety of thioflavanones have been synthesized from easily accessible 2′-iodochalcones or 2′-bromochalco

Cycloaddition of Benzothiete to 4-Substituted Styrenes

Meier, Herbert,Schmidt, Michael,Eckes, Heinz-Ludwig

, p. 1545 - 1550 (2007/10/02)

By thermal ring opening benzothiete (1) generates an 8-? electron system 2, which forms the cycloadducts 4/5a-j with 4-substituted styrenes 3a-j.The enhancement of the reactivity by electron-donating as well as electron-withdrawing substituents and their influence on the regioselectivity are discussed by applying frontier orbital calculations. - Key Words: Cycloaddition; Substituent effects; Reactivity; Regioselectivity; FMO calculations

Chemotherapeutic agents

-

, (2008/06/13)

A method of treating or preventing viral infections, in particular rhinovirus infections comprising the administration of an effective amount of a 2-phenyltetralin derivative or a heterocyclic analogue thereof. Pharmaceutical compositions containing these compounds, and some novel compounds are also disclosed.

A Convenient Synthesis of 2-Phenylbenzothiopyrylium Perchlorates

Nakazumi, Hiroyuki,Ueyama, Tamio,Endo, Takashi,Kitao, Teijiro

, p. 1251 - 1252 (2007/10/02)

2-Phenylbenzothiopyrylium perchlorates were conveniently prepared in good yields by reduction of 2-phenyl-4H-benzothiopyran-4-ones (thioflavones) with aluminium hydride, followed by treatment with acid in the presence of 2,3-dichloro-5,6-dicyano-p-b

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