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153827-73-7

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153827-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153827-73-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,8,2 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 153827-73:
(8*1)+(7*5)+(6*3)+(5*8)+(4*2)+(3*7)+(2*7)+(1*3)=147
147 % 10 = 7
So 153827-73-7 is a valid CAS Registry Number.

153827-73-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(benzenesulfonyl)-3-phenylindole

1.2 Other means of identification

Product number -
Other names N-benzenesulphonyl-2-phenylindole

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:153827-73-7 SDS

153827-73-7Relevant articles and documents

Rationally designed N-phenylsulfonylindoles as a tool for the analysis of the non-basic 5-HT6R ligands binding mode

Staroń, Jakub,Bugno, Ryszard,Pietru?, Wojciech,Sata?a, Grzegorz,Mordalski, Stefan,Warszycki, Dawid,Hogendorf, Agata,Hogendorf, Adam S.,Kalinowska-T?u?cik, Justyna,Lenda, Tomasz,Pilarski, Bogus?aw,Bojarski, Andrzej J.

supporting information, (2020/10/26)

Among all of the monoaminergic receptors, the 5-HT6R has the highest number of non-basic ligands (approximately 5% of compounds stored in 25th version of ChEMBL database have the strongest basic pKa below 5, calculated using the Instant JChem c

Palladium-Catalyzed Regioselective Synthesis of 3-Arylindoles from N-Ts-Anilines and Styrenes

Youn, So Won,Ko, Tae Yun,Jang, Young Ho

, p. 6636 - 6640 (2017/05/29)

A Pd-catalyzed intermolecular oxidative annulation between N-Ts-anilines and styrenes was developed. This method offers a straightforward and robust approach to a wide range of 3-arylindoles using readily available starting materials with good functional-group tolerance and high regioselectivity and efficiency. Further elaboration of the products obtained from this process provided access to highly functionalized and structurally diverse indoles, for example, 3-(indol-3-yl)carbazoles, 1,9-dihydropyrrolo-[2,3-b]carbazoles, and 3′-aryl-3,5′-biindoles.

Synthesis and pharmacological evaluation of indole-based sigma receptor ligands

Mésangeau, Christophe,Amata, Emanuele,Alsharif, Walid,Seminerio, Michael J.,Robson, Matthew J.,Matsumoto, Rae R.,Poupaert, Jacques H.,McCurdy, Christopher R.

experimental part, p. 5154 - 5161 (2011/11/29)

A series of novel indole-based analogs were prepared and their affinities for sigma receptors were determined using in vitro radioligand binding assays. The results of this study identified several compounds with nanomolar sigma-2 affinity and significant

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