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54544-05-7

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54544-05-7 Usage

General Description

Methyl 3,4-bis(benzyloxy)benzoate is a chemical compound that belongs to the ester family. It is commonly used as a fragrance ingredient, as well as a flavoring agent in the food industry. The compound is synthesized through the reaction of benzoic acid and methanol, followed by esterification with benzyl alcohol. Methyl 3,4-bis(benzyloxy)benzoate is also utilized as an intermediate in the production of various pharmaceuticals and agrochemicals. It is a white, crystalline solid with a sweet, floral odor, and it is soluble in organic solvents such as ethanol and acetone. Methyl 3,4-bis(benzyloxy)benzoate should be handled and stored according to standard safety procedures.

Check Digit Verification of cas no

The CAS Registry Mumber 54544-05-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,5,4 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54544-05:
(7*5)+(6*4)+(5*5)+(4*4)+(3*4)+(2*0)+(1*5)=117
117 % 10 = 7
So 54544-05-7 is a valid CAS Registry Number.

54544-05-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3,4-bis(phenylmethoxy)benzoate

1.2 Other means of identification

Product number -
Other names Benzoic acid,3,4-bis(phenylmethoxy)-,methyl ester

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:54544-05-7 SDS

54544-05-7Relevant articles and documents

Cannabidiol derivative, preparation method and application thereof

-

, (2021/07/28)

The invention discloses a cannabidiol derivative, a preparation method and application thereof, and belongs to the technical field of medicinal chemistry, wherein the cannabidiol derivative is obtained by taking cannabidiol as a main body through a synthesis means, and an anti-tumor activity determination result shows that the cannabidiol derivative prepared by the invention has an inhibition effect on lung cancer cell strains, human breast cancer cell strains, nasopharynx cancer and drug-resistant strains thereof.

Discovery and evaluation of the hybrid of bromophenol and saccharide as potent and selective protein tyrosine phosphatase 1B inhibitors

Zhang, Renshuai,Yu, Rilei,Xu, Qi,Li, Xiangqian,Luo, Jiao,Jiang, Bo,Wang, Lijun,Guo, Shuju,Wu, Ning,Shi, Dayong

supporting information, p. 24 - 33 (2017/04/11)

Protein tyrosine phosphatase 1B (PTP1B) is a key negative regulator of insulin signaling pathway. Inhibition of PTP1B is expected to improve insulin action. Appropriate selectivity and permeability are the gold standard for excellent PTP1B inhibitors. In this work, molecular hybridization-based screening identified a selective competitive PTP1B inhibitor. Compound 10a has IC50 values of 199?nM against PTP1B, and shows 32-fold selectivity for PTP1B over the closely related phosphatase TCPTP. Molecule docking and molecular dynamics studies reveal the reason of selectivity for PTP1B over TCPTP. Moreover, the cell permeability and cellular activity of compound 10a are demonstrated respectively.

Efficient synthesis of the siderophore petrobactin via antimony triethoxide mediated coupling

Pandey, Rajesh K.,Jarvis, Gregory G.,Low, Philip S.

scheme or table, p. 1627 - 1629 (2012/04/17)

Chemical synthesis of petrobactin, a siderophore for Bacillus anthracis, has been achieved via Sb(OEt)3-mediated ester-amide exchange.

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