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73620-18-5

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73620-18-5 Usage

General Description

Methyl (4-formylphenoxy)acetate is a chemical compound that belongs to the class of aromatic esters. It is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and organic compounds. The compound is often utilized in organic chemistry research for the development of new drugs and other bioactive molecules. Methyl (4-formylphenoxy)acetate is a colorless liquid with a fruity odor and is insoluble in water but soluble in organic solvents. It is important to handle and store this chemical with care as it can be potentially hazardous if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 73620-18-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,2 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73620-18:
(7*7)+(6*3)+(5*6)+(4*2)+(3*0)+(2*1)+(1*8)=115
115 % 10 = 5
So 73620-18-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H10O4/c1-13-10(12)7-14-9-4-2-8(6-11)3-5-9/h2-6H,7H2,1H3

73620-18-5SDS

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 Methyl 2-(4-formylphenoxy)acetate

1.2 Other means of identification

Product number -
Other names methyl 2-(4-formylphenoxy)acetate

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:73620-18-5 SDS

73620-18-5Relevant articles and documents

Synthesis and antileukemic activity of 16E-[4-(2-carboxy)ethoxybenzylidene] -androstene amides

Bansal, Ranju,Acharya, Pratap Chandra

, p. 552 - 557 (2012)

In order to determine the structural requirements for cytotoxicity against various tumor cell lines, a new series of 16E-arylidene androstene amides with varying degrees of unsaturation in ring A has been synthesized. Characterization and in vitro cytotox

INHIBITORS OF SHORT-CHAIN DEHYDROGENASE ACTIVITY FOR PROMOTING NEUROGENESIS AND INHIBITING NERVE CELL DEATH

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Paragraph 00285, (2018/02/27)

A method of promoting neuroprotection in a subject from axonal degeneration, neuronal cell death, and/or glia cell damage after injury, augmenting neuronal signaling underlying learning and memory, stimulating neuronal regeneration after injury, and/or treating a disease, disorder, and/or condition of the nervous system in a subject in need thereof includes administering to the subject a therapeutically effective amount of a 15-PGDH inhibitor.

INHIBITORS OF SHORT-CHAIN DEHYDROGENASE ACTIVITY FOR TREATING FIBROSIS

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Paragraph 00296, (2016/09/26)

A method of treating or preventing a fibrotic disease, disorder or condition includes administering to a subject in need of treatment a 15-PGDH inhibitor.

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