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4-(Isocyanatosulfonyl)-anisole, also known as 4-methoxyphenyl isothiocyanate, is an organic compound with the chemical formula C8H7NOS. It is a colorless to pale yellow liquid that is soluble in organic solvents. 4-(Isocyanatosulfonyl)-anisole is characterized by the presence of an isothiocyanate group (-N=C=S) attached to a 4-methoxyphenyl ring. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity, it is important to handle this chemical with care, as it can react with nucleophiles and form various derivatives.

7018-76-0

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7018-76-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7018-76-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,1 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7018-76:
(6*7)+(5*0)+(4*1)+(3*8)+(2*7)+(1*6)=90
90 % 10 = 0
So 7018-76-0 is a valid CAS Registry Number.

7018-76-0SDS

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 4-methoxy-N-(oxomethylidene)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names p-methoxyphenylsulphonyl isocyanate

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:7018-76-0 SDS

7018-76-0Relevant academic research and scientific papers

NMDA antagonists

-

, (2008/06/13)

The present invention is directed to a new class of 4-sulfanimide-quinoline derivatives and to their use as NMDA antagonists.

Mild and Efficient Synthesis of Aromatic Sulfonamides by in situ Preparation of the Corresponding Sulfonyl Isothiocyanates

Arnswald, Martin,Neumann, Wilhelm P.

, p. 1997 - 2000 (2007/10/02)

A new reaction between chlorosulfonyl isocyanate (1) and trialkylstannyl-substituted arenes 2a-k, 7, 9 is described.It provides the aromatic sulfonyl isocyanates 3 or their derivatives, the sulfonamides 4a-j, the sulfonylcarbamates 5a-b, or sulfonylureas 6, respectively.The trialkylstannyl group as an efficient leaving group allows mild reaction conditions to be applied and unusual substitution patterns to be obtained, normally not accessible by electrophilic aromatic substitutions.Thus, sulfonamidation can be achieved in meta position to a trifluoromethyl group. Key words: Electrophilic aromatic substitution; sulfodestannalytion; isocyanates, sulfonyl, aromatic; sulfonyl compounds; trialkylarylstannanes, application of

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