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18271-18-6

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18271-18-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18271-18-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,7 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18271-18:
(7*1)+(6*8)+(5*2)+(4*7)+(3*1)+(2*1)+(1*8)=106
106 % 10 = 6
So 18271-18-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H15NO2S/c1-13-6-10-17(11-7-13)21(19,20)18-16-9-8-14-4-2-3-5-15(14)12-16/h2-12,18H,1H3

18271-18-6SDS

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 4-methyl-N-naphthalen-2-ylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-[2]naphthyl-toluene-4-sulfonamide

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:18271-18-6 SDS

18271-18-6Relevant articles and documents

Modular Two-Step Access to π-Extended Naphthyridine Systems—Potent Building Blocks for Organic Electronics

Stuck, Fabian,Dietl, Martin C.,Mei?ner, Maximilian,Sebastian, Finn,Rudolph, Matthias,Rominger, Frank,Kr?mer, Petra,Hashmi, A. Stephen K.

supporting information, (2021/12/14)

Efficient synthetic approaches for the incorporation of nitrogen into polyaromatic compounds (PACs) in different patterns as stabilising moiety for π-extended systems and modification tool for optoelectronic properties remain a challenge until today. Here

Transition-metal-free synthesis of aromatic amines via the reaction of benzynes with isocyanates

Seo, Jeong Hoon,Ko, Haye Min

supporting information, p. 671 - 674 (2018/01/19)

An unexpected reaction between benzynes and isocyanates to generate aromatic amines has been developed under transition-metal-free conditions. The in situ prepared anions formed through cleavage of the N–C bond in isocyanates, reacted with aryne precursor

CuI catalyzed sulfamidation of arylboronic acid using TsNBr2 at room temperature

Loukrakpam, Dineshwori Chanu,Phukan, Prodeep

supporting information, p. 4855 - 4858 (2017/11/29)

An expeditious protocol for amidation arylboronic acid has been developed using TsNBr2 as the nitrogen source in presence of a CuI as catalyst. Various arylboronic acids could be transformed into corresponding N-arylsulfonamide derivatives within a very short time using CuI as catalyst in presence of DBU at room temperature.

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