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Benzene, 2-nitro-1,3-bis(phenylthio)-, also known as 2-nitro-1,3-bis(phenylthio)benzene, is an organic compound that serves as an intermediate in the synthesis of pharmaceuticals. It is characterized by a benzene ring with a nitro group at the 2-position and two phenylthio groups attached to the 1 and 3 positions, respectively.

98119-89-2

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98119-89-2 Usage

Uses

Used in Pharmaceutical Industry:
Benzene, 2-nitro-1,3-bis(phenylthio)is used as an intermediate in the synthesis of 9-Chloro Quetiapine (C366040), which is an impurity of Quetiapine hemifumarate (Q510000). Quetiapine hemifumarate is a dibenzothiazepine antipsychotic medication used in the treatment of schizophrenia. The synthesis of this intermediate plays a crucial role in the production of effective antipsychotic drugs, contributing to the management and treatment of mental health disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 98119-89-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,1,1 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 98119-89:
(7*9)+(6*8)+(5*1)+(4*1)+(3*9)+(2*8)+(1*9)=172
172 % 10 = 2
So 98119-89-2 is a valid CAS Registry Number.

98119-89-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-nitro-1,3-bis(phenylsulfanyl)benzene

1.2 Other means of identification

Product number -
Other names Benzene,2-nitro-1,3-bis(phenylthio)

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:98119-89-2 SDS

98119-89-2Relevant academic research and scientific papers

2,6-Bis(arylsulfonyl)anilines as fluorescent scaffolds through intramolecular hydrogen bonds: Solid-state fluorescence materials and turn-on-type probes based on aggregation-induced emission

Beppu, Teruo,Kawata, So,Aizawa, Naoya,Pu, Yong-Jin,Abe, Yasuyuki,Ohba, Yoshihiro,Katagiri, Hiroshi

, p. 536 - 545 (2014/05/06)

A series of 2,6-bis[aryl(alkyl)sulfonyl]anilines were synthesized by nucleophilic aromatic substitution of 2,6-dichloronitrobenzene with various aryl or alkyl thiolates (benzyl-, phenyl-, 2-naphthyl-, and 2-aminophenyl thiolate), followed by hydrogenation

Improved Inhibitors of Trypanothione Reductase by Combination of Motifs: Synthesis, Inhibitory Potency, Binding Mode, and Antiprotozoal Activities

Eberle, Christian,Lauber, Birgit Sophia,Fankhauser, Daniel,Kaiser, Marcel,Brun, Reto,Krauth-Siegel, R. Luise,Diederich, Francois

experimental part, p. 292 - 301 (2012/01/11)

Trypanothione reductase (TR) is an essential enzyme in the trypanothione-based redox metabolism of trypanosomatid parasites. This system is absent in humans and, therefore, offers a promising target for the development of selective new drugs against Afric

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