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Ethyl 4-methoxy-2-methylbenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56427-62-4

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56427-62-4 Usage

Synthesis Reference(s)

Tetrahedron Letters, 31, p. 481, 1990 DOI: 10.1016/0040-4039(90)87013-P

Check Digit Verification of cas no

The CAS Registry Mumber 56427-62-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,4,2 and 7 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56427-62:
(7*5)+(6*6)+(5*4)+(4*2)+(3*7)+(2*6)+(1*2)=134
134 % 10 = 4
So 56427-62-4 is a valid CAS Registry Number.

56427-62-4SDS

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 ethyl 4-methoxy-2-methylbenzoate

1.2 Other means of identification

Product number -
Other names ethyl 2-methyl-4-methoxybenzoate

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:56427-62-4 SDS

56427-62-4Relevant academic research and scientific papers

Practical: In situ -generation of phosphinite ligands for palladium-catalyzed carbonylation of (hetero)aryl bromides forming esters

Wang, Lin,Neumann, Helfried,Spannenberg, Anke,Beller, Matthias

supporting information, p. 7469 - 7472 (2017/07/12)

An effective method for alkoxycarbonylation of (hetero)aryl bromides is developed in the presence of in situ-generated phosphinite ligands tBu2POR (R = nBu, nPr, Et or Me). For this purpose commercially available tBu2PCl was used as the pre-ligand in the presence of different alcohols. For the first time cross coupling reactions with two alcohols-one generating the ligand, the other used as substrate-were developed. Through this method, ligand optimization can be performed in a more efficient manner and the desired products could be obtained with good yields and selectivity.

ISOINDOLINE COMPOUNDS FOR THE TREATMENT OF SPINAL MUSCULAR ATROPHY AND OTHER USES

-

Page/Page column 69, (2009/05/29)

Disclosed is a compound of Formula (I) in which W and R1-R6 are defined herein. Also disclosed is a method of treating spinal muscular atrophy, as well as methods of using such compounds to increase SMN expression, increase EAAT2 expression, or increase the expression of a nucleic acid that encodes a translational stop codon introduced directly or indirectly by mutation or frameshift.

[18F]-labeled isoindol-1-one and isoindol-1,3-dione derivatives as potential PET imaging agents for detection of β-amyloid fibrils

Lee, Ji Hoon,Byeon, Seong Rim,Kim, YoungSoo,Lim, Soo Jeong,Oh, Seung Jun,Moon, Dae Hyuk,Yoo, Kyung Ho,Chung, Bong Young,Kim, Dong Jin

scheme or table, p. 5701 - 5704 (2009/07/18)

In this study a novel series of isoindol-1-one and isoindol-1,3-dione derivatives for β-amyloid-specific binding agents is described. Twelve compounds were synthesized and evaluated via a competitive binding assay with [125I]TZDM against β-amyl

A Rapid Entry to Highly Functionalized p-Methoxybenzoates: Synthesis of Aromatic Portion of Milbemycin β3

Kotnis, Atul S.

, p. 481 - 484 (2007/10/02)

A wide variety of easily accessable Hagemann's esters are converted to p-methoxybenzoates with iodine and methanol.

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