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15448-94-9

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15448-94-9 Usage

Type

Organic compound

Molecular structure

Contains a benzene ring with a sulfonamide group and a hydroxy(diphenyl)methyl group attached

Potential applications

Pharmaceuticals, due to sulfonamide derivatives having antibacterial, diuretic, and antidiabetic properties

Additional biological activities

The hydroxy(diphenyl)methyl group may also have biological activities

Overall

Complex chemical compound with potential therapeutic uses

Check Digit Verification of cas no

The CAS Registry Mumber 15448-94-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,4 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15448-94:
(7*1)+(6*5)+(5*4)+(4*4)+(3*8)+(2*9)+(1*4)=119
119 % 10 = 9
So 15448-94-9 is a valid CAS Registry Number.

15448-94-9SDS

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 2-[hydroxy(diphenyl)methyl]-N-phenylbenzenesulfonamide

1.2 Other means of identification

Product number -
Other names 2-(diphenyl-hydroxy-methyl)-N-phenyl-benzenesulfonamide

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:15448-94-9 SDS

15448-94-9Relevant articles and documents

Short-Chain Branched Polar-Functionalized Linear Polyethylene via "tandem Catalysis"

Jian, Zhongbao,Mecking, Stefan

, p. 4057 - 4066 (2016/07/06)

Cationic PdII complex 1 chelated by an N-fixed phosphine sultam has been synthesized and structurally characterized. Exposure of 1 to ethylene resulted in the formation of short-chain olefins (1-butene: 2-butene: 1-hexene: 1-octene = 86:7:6:1) with a high catalytic activity of 105 molE molPd-1 h-1. By combination of 1 and one of the well-known phosphinesulfonato PdII catalyst precursors 2-5, linear polyethylenes containing methyl, ethyl, and n-butyl branches of up to 100 per 1000 C were generated from the polymerization of ethylene alone in a "tandem catalysis" one-pot approach. In further exploitation of this concept, linear polyethylenes with both various short-chain branches and a choice of different polar functional groups incorporated into the main chain were obtained for the first time from the copolymerization of ethylene and polar vinyl monomers (methyl acrylate, N-isopropylacrylamide, methyl vinyl sulfone, acrylonitrile, ethyl vinyl ether, vinyl acetate, and allyl bromide). All these apolar and polar branches are incorporated into the linear polyethylene backbones to varying degrees, while the type of initiating and terminating chain ends of the resulting polyethylenes depends significantly on the nature of polar vinyl monomer.

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