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Benzene, 1-iodo-2-(phenylthio)-, also known as 1-iodo-2-phenylthiobenzene, is an organic compound with the chemical formula C12H9IS. It is a derivative of benzene, featuring an iodine atom at the 1-position and a phenylthio group (a phenyl group bonded to a sulfur atom) at the 2-position. Benzene, 1-iodo-2-(phenylthio)- is characterized by its aromatic structure and the presence of a halogen (iodine) and a heteroatom (sulfur), which can influence its reactivity and properties. It is used in various chemical reactions and synthesis processes, particularly in the preparation of pharmaceuticals and other organic compounds. Due to its potential reactivity and the presence of a heavy halogen, it is important to handle Benzene, 1-iodo-2-(phenylthio)- with care, following appropriate safety protocols.

2236-42-2

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2236-42-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2236-42-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,3 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2236-42:
(6*2)+(5*2)+(4*3)+(3*6)+(2*4)+(1*2)=62
62 % 10 = 2
So 2236-42-2 is a valid CAS Registry Number.

2236-42-2Relevant academic research and scientific papers

Properties modulation of organic semi-conductors based on a donor-spiro-acceptor (D-spiro-A) molecular design: New host materials for efficient sky-blue PhOLEDs

Romain, Maxime,Tondelier, Denis,Jeannin, Olivier,Geffroy, Bernard,Rault-Berthelot, Jo?lle,Poriel, Cyril

, p. 9701 - 9714 (2015)

Four high triplet organic semi-conductors based on the donor-spiro-acceptor design (D-spiro-A) have been synthesized. Their physicochemical and photophysical properties have been studied, compared and discussed in light of the nature of their respective donor/acceptor units. The four compounds have been used as host materials in efficient sky-blue (EQE > 10% at 10 mA cm-2) phosphorescent organic light emitting diodes.

Solution-processed white organic light-emitting diodes with bi-component emitting layer based on symmetry blue spiro-sulfone derivative

Wang, Ruifang,Liu, Yanwei,Hu, Taiping,Wei, Xiaofang,Liu, Jianjun,Li, Zhiyi,Hu, Xiaoxiao,Yi, Yuanping,Wang, Pengfei,Wang, Ying

, p. 24 - 30 (2019)

We report a white organic light-emitting diode (WOLED)of simple construction with a bi-component emitting layer, in which a novel, dual-role deep blue TADF emitter as both the non-doped blue emitter and efficient host of an orange TADF emitter of TXO-TPA.

Structure and Reactivity of N-Heterocyclic Alkynyl Hypervalent Iodine Reagents

Le Du, Eliott,Duhail, Thibaut,Wodrich, Matthew D.,Scopelliti, Rosario,Fadaei-Tirani, Farzaneh,Anselmi, Elsa,Magnier, Emmanuel,Waser, Jerome

supporting information, p. 10979 - 10986 (2021/06/08)

Ethynylbenziodoxol(on)e (EBX) cyclic hypervalent iodine reagents have become popular reagents for the alkynylation of radicals and nucleophiles, but only offer limited possibilities for further structure and reactivity fine-tuning. Herein, the synthesis o

Thioxanthene and dioxothioxanthene dihydroindeno[2,1-b]fluorenes: Synthesis, properties and applications in green and sky blue phosphorescent OLEDs

Romain, Maxime,Quinton, Cassandre,Tondelier, Denis,Geffroy, Bernard,Jeannin, Olivier,Rault-Berthelot, Jo?lle,Poriel, Cyril

, p. 1692 - 1703 (2016/03/01)

We report herein the synthesis, and structural, electrochemical and photophysical properties of new dihydroindeno[2,1-b]fluorene-based semi-conductors, i.e. dispiro[thioxanthene-9,5′-indeno[2,1-b]fluorene-7′,9′′-thioxanthene] 2 and dispiro-[dioxothioxanth

Copper-catalyzed selective single arylsulfanylation of aryl diiodides with aryl thiols

Liu, Yunyun,Wang, Hang,Cao, Xiaoji,Fang, Zheng,Wan, Jie-Ping

, p. 2977 - 2982 (2013/11/06)

Selective single arylsulfanylation reactions of aryl diiodides with aryl or hetaryl thiols to give a broad array of iodine-functionalized sulfides were developed. Further elaboration of the iodine-containing products to provide a variety of aryl and hetaryl sulfides through coupling reactions was also demonstrated. Georg Thieme Verlag Stuttgart, New York.

Synthesis of molecular chains: phenylene thioether and sulfoxide oligomers

Vicente, José,Abad, José A.,López-Nicolás, Rosa M.

, p. 6281 - 6288 (2008/09/21)

The application of a general synthetic approach to prepare molecular chains is reported. It is based on a step-by-step method each consisting first in a Pd-catalyzed reaction between ArI and HXAr′Br (Ar=aryl, Ar′=arylene) to give ArXAr′Br followed by a Cu

Preparation of functionalized aryl magnesium reagents by the addition of magnesium aryl thiolates and amides to arynes

Lin, Wenwei,Sapountzis, Ioannis,Knochel, Paul

, p. 4258 - 4261 (2007/10/03)

(Chemical Equation Presented) Reactive arynes, which are readily generated by the reaction of ortho-iocloarylsulfonates with iPrMgCl, undergo the smooth addition of various magnesium nucleophiles like magnesium thiolates, selenides, and amides. In all cases the resulting functionalized aryl magnesium species can be trapped by an electrophile leading to highly functionalized aromatic compounds (see scheme).

Aromatic nucleophilic polysubstitution by sequential SRN1 reactions

Beugelmans, Rene,Chbani, Mohamed

, p. 290 - 305 (2007/10/02)

Substitution of aromatics (benzene, naphthalene and pyridine) by two or three distinct nucleophiles derived from phosphonates and/or thiolates can be performed by sequential photosimulated SRN1 reactions whose radical chain mechanism is compatible with the successively introduced substituents. aromatic polysubstitution / SRN1 mechanism / disubstituted aromatic / trisubstituted aromatic / distinct substituent

Intramolecular Cyclization to 1-Phenyl-1-benzothiophenium Salts by Electrophilic Addition of o-(Phenylsulfanyl)phenylalkynes

Kitamura, Tsugio,Takachi, Tatsuya,Miyaji, Masa-aki,Kawasato, Hironobu,Taniguchi, Hiroshi

, p. 1907 - 1912 (2007/10/02)

Electrophilic addition of 1--2-(p-methoxyphenyl)ethyne with electrophiles such as perchloric acid, tetrafluoroboric acid, bromine, and benzenesulfenyl chloride gave 1-phenyl-1-benzothiophenium salts exclusively.The substituent ef

Syntheses and Thermal Behaviour of 9-Substituted 9-Thia-10-azaphenanthrenes

Shimizu, Hiroshi,Ikedo, Koji,Hamada, Koji,Ozawa, Michinori,Matsumoto, Harutoshi,et al.

, p. 1733 - 1747 (2007/10/02)

Synthetic approaches to a variety of 9-thia-10-azaphenanthrenes having various kinds of substituent at the 9-position were investigated.Their thermal stabilities were found to be depend strongly upon the nature of the substituents on the sulphur atom.Seve

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