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18962-05-5

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18962-05-5 Usage

Chemical Properties

clear colorless to yellow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 18962-05-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,6 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18962-05:
(7*1)+(6*8)+(5*9)+(4*6)+(3*2)+(2*0)+(1*5)=135
135 % 10 = 5
So 18962-05-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H12O2/c1-8(2)12-10-5-3-9(7-11)4-6-10/h3-8H,1-2H3

18962-05-5 Well-known Company Product Price

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  • Alfa Aesar

  • (A12760)  4-Isopropoxybenzaldehyde, 97%   

  • 18962-05-5

  • 1g

  • 282.0CNY

  • Detail
  • Alfa Aesar

  • (A12760)  4-Isopropoxybenzaldehyde, 97%   

  • 18962-05-5

  • 5g

  • 941.0CNY

  • Detail
  • Alfa Aesar

  • (A12760)  4-Isopropoxybenzaldehyde, 97%   

  • 18962-05-5

  • 25g

  • 2388.0CNY

  • Detail

18962-05-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-propan-2-yloxybenzaldehyde

1.2 Other means of identification

Product number -
Other names 4-Isopropoxybenzaldehyde

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:18962-05-5 SDS

18962-05-5Relevant articles and documents

NOVEL COMPOUNDS FOR SKIN LIGHTENING

-

Page/Page column 13, (2021/03/05)

Novel compounds are disclosed. Skin lightening composition comprising said compounds and method of skin lightening is disclosed too. In addition, method of synthesizing said novel compounds are disclosed.

Soluble/MOF-Supported Palladium Single Atoms Catalyze the Ligand-, Additive-, and Solvent-Free Aerobic Oxidation of Benzyl Alcohols to Benzoic Acids

Tiburcio, Estefanía,Greco, Rossella,Mon, Marta,Ballesteros-Soberanas, Jordi,Ferrando-Soria, Jesús,López-Haro, Miguel,Hernández-Garrido, Juan Carlos,Oliver-Meseguer, Judit,Marini, Carlo,Boronat, Mercedes,Armentano, Donatella,Leyva-Pérez, Antonio,Pardo, Emilio

, p. 2581 - 2592 (2021/02/16)

Metal single-atom catalysts (SACs) promise great rewards in terms of metal atom efficiency. However, the requirement of particular conditions and supports for their synthesis, together with the need of solvents and additives for catalytic implementation, often precludes their use under industrially viable conditions. Here, we show that palladium single atoms are spontaneously formed after dissolving tiny amounts of palladium salts in neat benzyl alcohols, to catalyze their direct aerobic oxidation to benzoic acids without ligands, additives, or solvents. With this result in hand, the gram-scale preparation and stabilization of Pd SACs within the functional channels of a novel methyl-cysteine-based metal-organic framework (MOF) was accomplished, to give a robust and crystalline solid catalyst fully characterized with the help of single-crystal X-ray diffraction (SCXRD). These results illustrate the advantages of metal speciation in ligand-free homogeneous organic reactions and the translation into solid catalysts for potential industrial implementation.

Syntheses and characterization of aryl-substituted pyrogallol[4]arenes and resorcin[4]arenes

Pfeiffer, Constance R.,Feaster, Kyle A.,Dalgarno, Scott J.,Atwood, Jerry L.

, p. 222 - 229 (2015/12/31)

Seven aryl-substituted pyrogallol[4]arenes and six aryl-substituted resorcin[4]arenes were synthesized through the acid catalyzed reaction of either pyrogallol or resorcinol with a specific alkoxybenzaldehyde. Single crystal X-ray data was obtained for all thirteen compounds. In order to determine the effect of the different pendent -R groups, four properties were investigated: π-π distance, inward tilt, twist angle, and the angle between the planes containing the pendent -R groups. Positioning of the -R groups, the carbon atom chain length of the -R groups, the number of upper-rim hydroxyl groups (resorcin[4]arene vs. pyrogallol[4]arene), and the number of substituted phenyl groups all influenced these four properties. The trends that develop are investigated and discussed.

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