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3-(2,5-dimethylphenyl)-2-methylpropanal is an organic compound with the molecular formula C12H16O. It is a colorless to pale yellow liquid with a strong, sweet, and floral odor. This chemical is primarily used as a fragrance ingredient in various consumer products, such as perfumes, cosmetics, and household products. It is also known as 2-methyl-3-(2,5-dimethylphenyl)propanal or 2,5-dimethyl-3-(2-methylpropyl)benzaldehyde. The compound is synthesized through a series of chemical reactions, and its structure consists of a 2-methylpropanal group attached to a 2,5-dimethylphenyl group. Due to its pleasant scent, it is widely used in the fragrance industry to create a variety of aromas, enhancing the overall sensory experience of the products it is incorporated into.

6884-40-8

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6884-40-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6884-40-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,8 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6884-40:
(6*6)+(5*8)+(4*8)+(3*4)+(2*4)+(1*0)=128
128 % 10 = 8
So 6884-40-8 is a valid CAS Registry Number.

6884-40-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2,5-dimethylphenyl)-2-methylpropanal

1.2 Other means of identification

Product number -
Other names 2-Methyl-3-<2,5-dimethyl-phenyl>-propionaldehyd

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:6884-40-8 SDS

6884-40-8Downstream Products

6884-40-8Relevant academic research and scientific papers

Oxidative coupling of benzenes with α,β-unsaturated aldehydes by the Pd(OAc)2/molybdovanadophosphoric acid/O2 system

Yamada, Tomoyuki,Sakaguchi, Satoshi,Ishii, Yasutaka

, p. 5471 - 5474 (2008/04/18)

The oxidative coupling reaction of benzene with an α,β- unsaturated aldehyde was examined by the combined catalytic system of Pd(OAc)2 with molybdovanadophosphoric acid (HPMoV) under atmospheric dioxygen. Thus, the reaction of benzene with acrolein under dioxygen (1 atm) by the use of catalytic amounts of Pd(OAc)2 and H4PMo 11VO40·26H2O in the presence of dibenzoylmethane as a ligand in propionic acid at 90 °C for 1.5 h afforded cinnamaldehyde in 59% yield and β-phenylcinnamaldehyde in 5% yield. This catalytic system was extended to the direct oxidative coupling through the C-H bond activation of various arenes with acrolein and methacrolein.

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