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51264-69-8

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51264-69-8 Usage

General Description

4-Formylphenoxyacetic acid ethyl ester is an organic compound that belongs to the ester class of chemicals. It is derived from the combination of 4-formylphenoxyacetic acid and ethyl alcohol. This chemical is commonly used in the synthesis of pharmaceuticals and agrochemicals due to its potential as a building block in organic chemistry. The ethyl ester form of 4-formylphenoxyacetic acid contributes to its solubility and stability in various organic solvents, making it a versatile and valuable chemical in the field of chemical research and manufacturing.

Check Digit Verification of cas no

The CAS Registry Mumber 51264-69-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,6 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 51264-69:
(7*5)+(6*1)+(5*2)+(4*6)+(3*4)+(2*6)+(1*9)=108
108 % 10 = 8
So 51264-69-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H12O4/c1-2-14-11(13)8-15-10-5-3-9(7-12)4-6-10/h3-7H,2,8H2,1H3

51264-69-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-(4-formylphenoxy)acetate

1.2 Other means of identification

Product number -
Other names Acetic acid, (4-formylphenoxy)-, ethyl 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:51264-69-8 SDS

51264-69-8Relevant articles and documents

EBNA1-specific luminescent small molecules for the imaging and inhibition of latent EBV-infected tumor cells

Jiang, Lijun,Lui, Yin-Lai,Li, Hongguang,Chan, Chi-Fai,Lan, Rongfeng,Chan, Wai-Lun,Lau, Terrence Chi-Kong,Tsao, George Sai-Wah,Mak, Nak-Ki,Wong, Ka-Leung

, p. 6517 - 6519 (2014)

An EBNA1-specific small molecule (JLP2) has been synthesised. As a strong binder and dimerization inhibitor of EBNA1 in vitro, JLP2 may be used as a selective luminescent agent for the imaging and inhibition of latent EBV-infected ca

PhotoTag: Photoactivatable Fluorophores for Protein Labeling

Fay, Rachael,Holland, Jason P.,Linden, Anthony

, (2020)

We report experimental studies on the development of photoactivatable fluorophores for rapid, light-induced synthesis of protein conjugates. Proof-of-concept studies demonstrated that electronic excitation of photoactivatable BODIPY-ArN3 (1) in

Synthesis and antinociceptive profile of novel acidic sulphonylhydrazone derivatives from natural safrole

Lima, Lidia M.,Amarante, Emanuel G.,Miranda, Ana L.P.,Fraga, Carlos A.M.,Barreiro, Eliezer J.

, p. 673 - 678 (1999)

The synthesis and antinociceptive activity of new sulphonylhydrazone derivatives is described. The synthetic route started from safrole, an abundant Brazilian natural product which occurs in sassafras oil (Ocotea pretiosa). The active compounds were obtai

Fluorescent multi-component polymer sensors for the sensitive and selective detection of Hg2+/Hg+ions: Via dual mode fluorescence and colorimetry

Cheng, Xinjian,Liu, Kaiqi,Marin, Luminita,Xiao, Li

, p. 22888 - 22901 (2021/12/24)

Multi-component polymers (MCPs) incorporate multiple components into the main chain or pendant group and have special functions. In this work, the small-molecule fluorescent boron-dipyrromethene (BODIPY), with ester groups and/or alkoxyl long chains, was synthesized first. Then, this small-molecule BODIPY and the components containing CC bonds (HD and PD) were reacted via the Heck coupling reaction to obtain macromolecular probes that perform different functions. With the help of ester groups and alkoxyl "tail", polymers MCP1 and MCP2 were soluble in a variety of water-miscible organic solvents. Moreover, MCP3 and MCP4 were completely soluble in water. These macromolecular probes showed sensitive and selective recognition toward Hg2+/Hg+ because of the introduced components (HD and PD) containing CC bonds. After binding to Hg2+/Hg+, MCP1 and MCP2 demonstrated fluorescence quenching and color changes, which allowed the dual-channel specific detection of Hg2+/Hg+. Compared with the probes containing HD, the probes containing PD showed higher sensitivity, and the good recognition ability caused the detection limit to be as low as 0.32 μM, which may be due to the "molecular wire"mechanism. The small-molecule components with different functional groups were polymerized into fluorescent polymer materials. This methodology endows the polymer probe with good solubility and high sensitivity, and the as-prepared polymers could sense metal ions in aqueous environments. This journal is

Acylhydrazone derivative containing phosphonate and preparation method and application thereof

-

Paragraph 0024; 0026; 0027; 0028; 0029, (2020/03/12)

The invention discloses an acylhydrazone derivative containing phosphonate and a preparation method and application thereof. The structural general formula of the acylhydrazone derivative containing phosphonate is as shown in the specification. According

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