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17374-48-0

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  • N-[2-[[[3-hydroxy-5-[[oxo-[2-[[oxo(2-pyridinylmethoxy)methyl]amino]phenyl]methyl]amino]-1,6-diphenylhexan-2-yl]amino]-oxomethyl]phenyl]carbamic acid 2-pyridinylmethyl ester

    Cas No: 17374-48-0

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17374-48-0 Usage

General Description

SALICYLIC ACID 4-NITROPHENYL ESTER, also known as 4-Nitrophenyl salicylate, is a chemical compound commonly used in the production of a variety of pharmaceuticals, dyes, and pigments. It is derived from salicylic acid and 4-nitrophenol, and is typically found in the form of a white to light yellow crystalline powder. As an ester of salicylic acid, it exhibits similar properties to its parent compound, including anti-inflammatory and anti-bacterial properties. 4-Nitrophenyl salicylate is also known for its use as a substrate in enzyme kinetic assays, particularly in the study of esterase activity. Its versatility and applications in various industries make it a valuable and widely used chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 17374-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,7 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17374-48:
(7*1)+(6*7)+(5*3)+(4*7)+(3*4)+(2*4)+(1*8)=120
120 % 10 = 0
So 17374-48-0 is a valid CAS Registry Number.

17374-48-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Nitrophenyl Salicylate

1.2 Other means of identification

Product number -
Other names (4-nitrophenyl) 2-hydroxybenzoate

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:17374-48-0 SDS

17374-48-0Relevant articles and documents

Synthesis of salicylates from anionically activated aromatic trifluoromethyl group

Lin, Chuankai,Liu, Jin-Biao,Wang, Ruixiang,Xie, Huilin

supporting information, (2021/12/22)

An efficient approach to salicylates via a novel transformation of anionically activated aromatic trifluoromethyl group is described. Anionically activated trifluoromethyl group can react with phenols/alcohols under alkaline conditions to afford aryl/alkyl salicylates in high yields. Mechanism studies indicate that the carbonyl oxygen atom of ester is from the H2O in the solvent.

Preparation of phenol-protein conjugates by reaction of proteins with acetylated hydroxybenzoic acid nitrophenyl esters

Wagner,Hanfeld

, p. 739 - 741 (2007/10/02)

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