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16358-36-4

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16358-36-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16358-36-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,5 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16358-36:
(7*1)+(6*6)+(5*3)+(4*5)+(3*8)+(2*3)+(1*6)=114
114 % 10 = 4
So 16358-36-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H15NO3S/c1-15(12-6-4-3-5-7-12)19(16,17)14-10-8-13(18-2)9-11-14/h3-11H,1-2H3

16358-36-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methoxy-N-methyl-N-phenylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names 1-(N-methyl-N-phenyl)sulfamoyl-4-methoxybenzene

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:16358-36-4 SDS

16358-36-4Downstream Products

16358-36-4Relevant articles and documents

Iodine-catalyzed sulfonylation of sulfonyl hydrazides with: Tert -amines: A green and efficient protocol for the synthesis of sulfonamides

Chen, Jinyang,Han, Xiaoran,Mei, Lan,Liu, Jinchuan,Du, Kui,Cao, Tuanwu,Li, Qiang

, p. 31212 - 31216 (2019/10/19)

This study provides a direct, sustainable and eco-friendly method for the synthesis of various sulfonamides via the sulfonylation of sulfonyl hydrazides with tert-amines. The method utilizes sulfonyl hydrazides to oxidize and couple with tertiary amines through selective cleavage of C-N bonds. In this reaction, molecular iodine was used as the catalyst and t-butyl hydroperoxide was used as the oxidant.

KMnO4-mediated oxidative C[sbnd]N bond cleavage of tertiary amines: Synthesis of amides and sulfonamides

Zhang, Zhang,Liu, Yong-Hong,Zhang, Xi,Wang, Xi-Cun

, p. 2763 - 2770 (2019/04/10)

KMnO4-mediated oxidative C[sbnd]N bond cleavage of tertiary amines producing secondary amine was introduced, which was trapped by electrophiles (acyl chloride and sulfonyl chloride) to form amides and sulfonamides. The reaction could take place at mild condition, tolerating a wide range of function groups and affording products in moderate to excellent yields.

Derivatives of p-substituted phenyl ester of pivalic acid

-

, (2008/06/13)

A derivative of general formula: STR1 wherein Y is --SO2 -- or STR2 (i) R1 and R2, which may be the same or different, each represent, (1) --H, (2) C1-16 alkyl or (3) the formula: --X-- A --(R4)n wher

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