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92991-64-5

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92991-64-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92991-64-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,9 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92991-64:
(7*9)+(6*2)+(5*9)+(4*9)+(3*1)+(2*6)+(1*4)=175
175 % 10 = 5
So 92991-64-5 is a valid CAS Registry Number.

92991-64-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-(4-formylphenoxy)butanoate

1.2 Other means of identification

Product number -
Other names -

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:92991-64-5 SDS

92991-64-5Relevant articles and documents

Tetrakis(ethyl-4(4-butyryl)oxyphenyl)porphyrinato zinc complexes with 4,4′-bpyridin: Synthesis, characterization, and its catalytic degradation of Calmagite

Soury, Raoudha,Jabli, Mahjoub,Saleh, Tawfik A.,Abdul-Hassan, Wathiq Sattar,Saint-Aman, Eric,Loiseau, Frédérique,Philouze, Christian,Nasri, Habib

, p. 20143 - 20156 (2018)

This work reports on the synthesis and characterization of a new porphyrins complex:[Zn(TEBOP)(4,4′-bpy)](4,4′-bipyridine)(5,10,15,20-(tetraethyl-4(4-butyryl)oxyphenyl)porphyrinato)zinc(ii) (3). Single crystal X-ray diffraction, photophysical and electroc

Superior Fluorogen-Activating Protein Probes Based on 3-Indole-Malachite Green

Zhang, Qingyang,Wang, Qinghua,Sun, Ying,Zuo, Limin,Fetz, Verena,Hu, Hai-Yu

, p. 4496 - 4499 (2017)

A series of novel fluorogenic dyes based on 3-indole-Malachite Green, MGs 5-7, have been developed that are dark in solution but highly fluorescent when bound to the cognate reporter, fluorogen-activating protein (FAP). Significantly, the new MGs 5-7 prob

Design of flexible dendritic systems bearing donor-acceptor groups (pyrene-porphyrin) for FRET applications

Ba?ales-Leal, Yoliztli,García-Rodríguez, Andrea,Cuétara-Guadarrama, Fabián,Vonlanthen, Mireille,Sorroza-Martínez, Kendra,Morales-Morales, David,Rivera, Ernesto

, (2021)

Herein, we report the synthesis and characterization of a novel series of dendritic compounds, bearing peripheral pyrene groups and a porphyrin core, of zero and first generation with different spacer lengths. These compounds were further metallated with

Microwave-assisted efficient synthesis of pyrazole-fibrate derivatives as stimulators of glucose uptake in skeletal muscle cells

Gupta, Sampa,Kant, Ruchir,Pandey, Shubham,Rai, Amit Kumar,Sashidhara, Koneni V.,Singh, L. Ravithej,Tamrakar, Akhilesh K.

supporting information, (2021/01/12)

The design and synthesis of a series of pyrazolo[3,4-d]pyrimidinones containing fibrate side chains have been accomplished by utilizing the concept of molecular hybridization. All the synthesized compounds were evaluated for the glucose uptake stimulatory effect in L6 rat skeletal muscle cells. Four compounds (3f, 3g, 3j and 3q) were found to show significant stimulation of glucose uptake. Further these four compounds have been examined for their Glut4 translocation stimulatory effect in L6-Glut4myc myotubes. Compound 3q was found to exert maximum increase in GLUT4myc translocation.

A Strategy to Prepare Peptide Heterodimers in the Solid Phase with an Acid-Labile Linker

Wang, Gang,Chen, Tingting,Peng, Tao,Zhang, Shouguo,Wang, Junyi,Wen, Xiaoxue,Yang, Xiaoming,Wang, Lin

supporting information, p. 7351 - 7355 (2019/10/02)

The currently synthetic methods of peptide heterodimer involve tedious synthesis and purification steps. An acid-labile traceless linker was prepared, which is highly compatible with the Fmoc strategy and could be used to prepare peptide heterodimer on re

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