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5736-85-6

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5736-85-6 Usage

Uses

4-Propoxybenzaldehyde was used in the preparation of (2S,4S,5R)-(±)-2-(4-propoxyphenyl)-3,4-dimethyl-5-phenyl-1,3-oxazolidine via condensation with 1-ephedrine.

General Description

Kinetic constants for the inhibition of the diphenolase activity of mushroom tyrosinase by 4-propoxybenzaldehyde was evaluated.

Check Digit Verification of cas no

The CAS Registry Mumber 5736-85-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,3 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5736-85:
(6*5)+(5*7)+(4*3)+(3*6)+(2*8)+(1*5)=116
116 % 10 = 6
So 5736-85-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O2/c1-2-7-12-10-5-3-9(8-11)4-6-10/h3-6,8H,2,7H2,1H3

5736-85-6 Well-known Company Product Price

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  • Alfa Aesar

  • (L08822)  4-n-Propoxybenzaldehyde, 97%   

  • 5736-85-6

  • 5g

  • 140.0CNY

  • Detail
  • Alfa Aesar

  • (L08822)  4-n-Propoxybenzaldehyde, 97%   

  • 5736-85-6

  • 25g

  • 467.0CNY

  • Detail

5736-85-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-N-PROPOXYBENZALDEHYDE

1.2 Other means of identification

Product number -
Other names 4-propoxybenzaldehyde

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:5736-85-6 SDS

5736-85-6Relevant articles and documents

Ambient Hydrogenation and Deuteration of Alkenes Using a Nanostructured Ni-Core–Shell Catalyst

Beller, Matthias,Feng, Lu,Gao, Jie,Jackstell, Ralf,Jagadeesh, Rajenahally V.,Liu, Yuefeng,Ma, Rui

supporting information, p. 18591 - 18598 (2021/06/28)

A general protocol for the selective hydrogenation and deuteration of a variety of alkenes is presented. Key to success for these reactions is the use of a specific nickel-graphitic shell-based core–shell-structured catalyst, which is conveniently prepared by impregnation and subsequent calcination of nickel nitrate on carbon at 450 °C under argon. Applying this nanostructured catalyst, both terminal and internal alkenes, which are of industrial and commercial importance, were selectively hydrogenated and deuterated at ambient conditions (room temperature, using 1 bar hydrogen or 1 bar deuterium), giving access to the corresponding alkanes and deuterium-labeled alkanes in good to excellent yields. The synthetic utility and practicability of this Ni-based hydrogenation protocol is demonstrated by gram-scale reactions as well as efficient catalyst recycling experiments.

Photoredox-Catalyzed Simultaneous Olefin Hydrogenation and Alcohol Oxidation over Crystalline Porous Polymeric Carbon Nitride

Qiu, Chuntian,Sun, Yangyang,Xu, Yangsen,Zhang, Bing,Zhang, Xu,Yu, Lei,Su, Chenliang

, p. 3344 - 3350 (2021/07/26)

Booming of photocatalytic water splitting technology (PWST) opens a new avenue for the sustainable synthesis of high-value-added hydrogenated and oxidized fine chemicals, in which the design of efficient semiconductors for the in-situ and synergistic utilization of photogenerated redox centers are key roles. Herein, a porous polymeric carbon nitride (PPCN) with a crystalline backbone was constructed for visible light-induced photocatalytic hydrogen generation by photoexcited electrons, followed by in-situ utilization for olefin hydrogenation. Simultaneously, various alcohols were selectively transformed to valuable aldehydes or ketones by photoexcited holes. The porosity of PPCN provided it with a large surface area and a short transfer path for photogenerated carriers from the bulk to the surface, and the crystalline structure facilitated photogenerated charge transfer and separation, thus enhancing the overall photocatalytic performance. High reactivity and selectivity, good functionality tolerance, and broad reaction scope were achieved by this concerted photocatalysis system. The results contribute to the development of highly efficient semiconductor photocatalysts and synergistic redox reaction systems based on PWST for high-value-added fine chemical production.

Synthesis and mesomorphic properties of coumarin derivatives with chalcone and imine linkages

Durgapal, Sunil Dutt,Soni, Rina,Soman, Shubhangi S.,Prajapati

, (2019/11/26)

We report here design and synthesis of two new mesogenic homologous series of coumarin derivatives consisting of chalcone and imine central linkages along with terminal n-alkoxy chain. All the compounds were synthesized and characterized by combination of elemental analysis and standard spectroscopic methods. All compounds were screened under polarising optical microscope (POM) for liquid crystalline properties, thermogram of all compounds were studied using differential scanning calorimetry (DSC) to get phase transition temperatures, enthalpy and entropy. X-ray single crystal study of n-octyloxy coumarin derivative 16 g was resolved with imine central linkage, which showed linear rod like geometry.

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