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19360-67-9

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19360-67-9 Usage

Chemical Properties

OFF-WHITE TO CREAM CRYSTALLINE POWDER

Check Digit Verification of cas no

The CAS Registry Mumber 19360-67-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,3,6 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 19360-67:
(7*1)+(6*9)+(5*3)+(4*6)+(3*0)+(2*6)+(1*7)=119
119 % 10 = 9
So 19360-67-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H8O5/c10-8(11)5-14-7-3-1-6(2-4-7)9(12)13/h1-4H,5H2,(H,10,11)(H,12,13)/p-2

19360-67-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(carboxymethoxy)benzoic acid

1.2 Other means of identification

Product number -
Other names p-(carboxymethyloxy)benzenecarboxylic acid

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:19360-67-9 SDS

19360-67-9Relevant articles and documents

Phase transfer catalyzed syntheses of 4-carboxylphenoxyacetic acid derivatives

Wang, Xicun,Li, Zheng,Da, Yuxia,Chen, Jichou,Wei, Taibao

, p. 4153 - 4161 (1999)

A series of new aryl 4-carboaryloxyphenoxyacetates (3a-e) and 4- carboanilinophenoxyacetanilides (3f-s) are synthesized by the reactions of 4- chloroformylphenoxyacetyl chloride with substituted phenols or aromatic amines via liquid-liquid phase transfer catalysis using PEG-400 as the catalyst.

Microwave (MW), ultrasound (US) and combined synergic MW-US strategies for rapid functionalization of pharmaceutical use phenols

Pawe?czyk, Anna,Sowa-Kasprzak, Katarzyna,Olender, Dorota,Zaprutko, Lucjusz

, (2018/09/26)

Increasingly stringent regulations aimed at protection of the natural environment have stimulated the search for new synthetic methodologies in organic and medicinal chemistry having no or minimum harmful effect. An interesting approach is the use of alternative activation factors, microwaves (MW) or ultrasounds (US) and also their cross-combination, which has been tested in the fast and efficient creation of new structures. At present, an easy and green hybrid strategy (“Lego” chemistry) is generally recommended for the design of new substances from different chemistry building blocks. Often, selected biologically active components with specific chemical reactivities are integrated by a suitably designed homo- or heterodifunctional linker that modifies the functionality of the starting structure, allowing easy covalent linkage to another molecule. In this study, a fast introduction of heterodifunctional halogenoacidic linker to selected mono-, di- and triphenolic active substances, allowing their functionalization, was investigated. Nucleophilic substitution reaction was chosen to produce final ethers with the reactive carboxylic group from phenols. The functionalization was performed using various green factors initiating and supporting the chemical reactions (MW, US, MW-US). The benefits of the three green supporting methods and different conditions of reactions were analyzed and compared with the results of the reaction performed by conventional methods.

PODOPHYLLOTOXIN DERIVATIVES AND THEIR USE

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Paragraph 0112; 0113; 0114, (2017/05/15)

Provided herein are compounds, compositions, and methods for treating cancer in a subject in need thereof.

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