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N-(1,3-BENZODIOXOL-5-YLMETHYL)METHANESULFONAMIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

184041-99-4

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184041-99-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 184041-99-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,0,4 and 1 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 184041-99:
(8*1)+(7*8)+(6*4)+(5*0)+(4*4)+(3*1)+(2*9)+(1*9)=134
134 % 10 = 4
So 184041-99-4 is a valid CAS Registry Number.

184041-99-4SDS

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 N-(3,4-methylenedioxy)benzyl-methanesulfonamide

1.2 Other means of identification

Product number -
Other names N-(1,3-BENZODIOXOL-5-YLMETHYL)METHANESULFONAMIDE

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:184041-99-4 SDS

184041-99-4Downstream Products

184041-99-4Relevant academic research and scientific papers

Biphenylsulfonamides and derivatives thereof that modulate the activity of endothelin

-

, (2008/06/13)

Biphenylsulfonamides and methods for modulating or altering the activity of the endothelin family of peptides are provided. In particular, bicyclic or tricyclic carbon or heterocyclic ring biphenylsulfonamides and methods using these sulfonamides for inhibiting the binding of an endothelin peptide to an endothelin receptor by contacting the receptor with the sulfonamide are provided. Methods for treating endothelin-mediated disorders by administering effective amounts of one or more of these sulfonamides or prodrugs thereof that inhibit or increase the activity of endothelin are also provided.

N-aryl thienyl-, furyl-, and pyrrolyl-sulfonamides and derivatives thereof that modulate the activity of endothelin

-

Page column 127, (2010/01/30)

Thienyl-, furyl- and pyrrolyl-sulfonamides and methods for modulating or altering the activity of the endothelin family of peptides are provided. In particular, N-(isoxazolyl)thienylsulfonamides, N-(isoxazolyl)furylsulfonamides and N-(isoxazolyl)pyrrolylsulfonamides and methods using these sulfonamides for inhibiting the binding of an endothelin peptide to an endothelin receptor by contacting the receptor with the sulfonamide are provided. Methods for treating endothelin-mediated disorders by administering effective amounts of one or more of these sulfonamides or prodrugs thereof that inhibit or increase the activity of endothelin are also provided.

Structure-activity relationships of N2-aryl-3-(isoxazolylsulfamoyl)-2- thiophenecarboxamides as selective endothelin receptor-A antagonists

Wu, Chengde,Chan, Ming F.,Stavros, Fiona,Raju,Okun, Ilya,Castillo, Rosario S.

, p. 1682 - 1689 (2007/10/03)

We report here that N2-aryl-3-(isoxazolylsulfamoyl)-2- thiophenecarboxamides are potent and selective small molecule ET(A) receptor antagonists. The aryl group was subjected to extensive structural modification. With monosubstitution, the para

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