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433230-57-0

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433230-57-0 Usage

Physical state

Pale yellow liquid.

Odor

Sweet, floral.

Usage

Commonly used as a fragrance ingredient in perfumes and other personal care products.

Potential applications

Synthesis of pharmaceuticals and other organic compounds.

Manufacturing method

Primarily manufactured through chemical synthesis.

Hazard classification

Moderately hazardous substance.

Handling precautions

Recommendations for proper handling and storage to minimize risks.

Check Digit Verification of cas no

The CAS Registry Mumber 433230-57-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,3,2,3 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 433230-57:
(8*4)+(7*3)+(6*3)+(5*2)+(4*3)+(3*0)+(2*5)+(1*7)=110
110 % 10 = 0
So 433230-57-0 is a valid CAS Registry Number.

433230-57-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,5-dimethylphenyl)acetaldehyde

1.2 Other means of identification

Product number -
Other names 2,5-Dimethylbenzeneacetaldehyde

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:433230-57-0 SDS

433230-57-0Relevant articles and documents

Maleimide-assisted anti-Markovnikov Wacker-type oxidation of vinylarenes using molecular oxygen as a terminal oxidant

Nakaoka, Sonoe,Murakami, Yuka,Kataoka, Yasutaka,Ura, Yasuyuki

supporting information, p. 335 - 338 (2016/01/09)

Arylacetaldehydes were successfully synthesized by the anti-Markovnikov Wacker-type oxidation of vinylarenes using 1 atm O2 as a terminal oxidant under mild conditions. Electron-deficient alkenes, such as maleic anhydride and maleimides, were effective additives and would operate as ligands to stabilize the Pd(0) species during the reaction.

Catalytic oxidation of alkenes with a surface-bound metalloporphyrin- peptide conjugate

Geier III, G. Richard,Sasaki, Tomikazu

, p. 1859 - 1870 (2007/10/03)

A novel surface-bound metalloporphyrin-peptide conjugate was prepared and used to catalytically oxidize alkenes in the presence of iodosylbenzene. The catalyst was found to oxidize a number of alkene substrates in good yield under a variety of reaction conditions. Comparison to control experiments using surface-bound Mn(III)tetraphenylporphyrin showed differences in oxidation yields and ratios of oxidized products. Substrate competition experiments demonstrated the ability of the conjugate catalyst to discriminate between substrates on the basis of size. Both results suggest oxidative catalysis occurred between the porphyrin ring and the peptide chain with the peptide influencing the outcome of the reaction in accord with the catalyst design.

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