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5779-94-2

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5779-94-2 Usage

Chemical Properties

CLEAR COLORLESS TO VERY SLIGHTLY YELLOW LIQUID

Uses

2,5-Dimethylbenzaldehyde is useful for building asymmetric top molecules. 2,5-DMBA has also been used to analyze vehicle carbon emissions.

General Description

The LD vehicle′s emmision factor for 2,5-dimethylbenzaldehyde was studied.

Check Digit Verification of cas no

The CAS Registry Mumber 5779-94-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,7 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5779-94:
(6*5)+(5*7)+(4*7)+(3*9)+(2*9)+(1*4)=142
142 % 10 = 2
So 5779-94-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H10O/c1-7-3-4-8(2)9(5-7)6-10/h3-6H,1-2H3

5779-94-2 Well-known Company Product Price

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  • Alfa Aesar

  • (L01924)  2,5-Dimethylbenzaldehyde, 98%   

  • 5779-94-2

  • 5g

  • 421.0CNY

  • Detail
  • Alfa Aesar

  • (L01924)  2,5-Dimethylbenzaldehyde, 98%   

  • 5779-94-2

  • 25g

  • 1399.0CNY

  • Detail

5779-94-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-Dimethylbenzaldehyde

1.2 Other means of identification

Product number -
Other names p-Xylylaldehyd

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:5779-94-2 SDS

5779-94-2Relevant articles and documents

A green approach for aerobic oxidation of benzylic alcohols catalysed by CuI-Y zeolite/TEMPO in ethanol without additional additives

Senthilkumar, Samuthirarajan,Zhong, Wei,Natarajan, Mookan,Lu, Chunxin,Xu, Binyu,Liu, Xiaoming

, p. 705 - 713 (2021/01/25)

An efficient and green protocol for aerobic oxidation of benzylic alcohols in ethanol using CuI-Y zeolite catalysts assisted by TEMPO (TEMPO = 2,2,6,6-tetramethyl-1-piperidine-N-oxyl) as the radical co-catalyst in the presence of atmospheric air under mild conditions is reported. The CuI-Y zeolite prepared via ion exchange between CuCl and HY zeolite was fully characterized by a variety of spectroscopic techniques including XRD, XPS, SEM, EDX and HRTEM. The incorporation of Cu(i) into the 3D-framework of the zeolite rendered the catalyst with good durability. The results of repetitive runs revealed that in the first three runs, there was hardly a decline in activity and a more substantial decrease in yield was observed afterwards, while the selectivity remained almost unchanged. The loss in activity was attributed to both the formation of CuO and the bleaching of copper into the liquid phase during the catalysis, of which the formation of CuO was believed to be the major contributor since the bleaching loss for each run was negligible (2%). In this catalytic system, except TEMPO, no other additives were needed, either a base or a ligand, which was essential in some reported catalytic systems for the oxidation of alcohols. The aerobic oxidation proceeded under mild conditions (60 °C, and 18 hours) to quantitatively and selectively convert a wide range of benzylic alcohols to corresponding aldehydes, which shows great potential in developing green and environmentally benign catalysts for aerobic oxidation of alcohols. The system demonstrated excellent tolerance against electron-withdrawing groups on the phenyl ring of the alcohols and showed sensitivity to steric hindrance of the substrates, which is due to the confinement of the pores of the zeolite in which the oxidation occurred. Based on the mechanism reported in the literature for homogenous oxidation, a mechanism was analogously proposed for the aerobic oxidation of benzylic alcohols catalysed by this Cu(i)-containing zeolite catalyst. This journal is

Production and testing of technical catalysts based on MnO2 for the abatement of aromatic volatile compounds at the laboratory and pilot plant scales

Baldovino-Medrano, Víctor Gabriel,Kartheuser, Beno?t,Gaigneaux, Eric M.

, p. 81 - 92 (2019/04/25)

Shaping is a crucial step to produce technical catalysts that remains as some sort of dark art for catalytic researchers in academia. This contribution discusses aspects concerning the fabrication of technical catalysts based on MnO2 powders ai

A Copper-Benzotriazole-Based Coordination Polymer Catalyzes the Efficient One-Pot Synthesis of (N′-Substituted)-hydrazo-4-aryl-1,4-dihydropyridines from Azines

Kallitsakis, Michael,Loukopoulos, Edward,Abdul-Sada, Alaa,Tizzard, Graham J.,Coles, Simon J.,Kostakis, George E.,Lykakis, Ioannis N.

supporting information, p. 138 - 145 (2017/01/14)

A series of new (N′-substituted)-hydrazo-4-aryl-1,4-dihydropyridines was successfully synthesized via a facile one-pot catalytic pathway utilizing azines and propiolate esters as starting materials and a one-dimensional copper benzotriazole-based coordination polymer as catalyst. In the absence of catalyst, the corresponding 5-substituted 4,5-dihydropyrazoles were formed in moderate to high yields. Fine-tuning of the catalysts allowed us to gain more insights regarding the plausible reaction mechanism. (Figure presented.).

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