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7148-78-9

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7148-78-9 Usage

General Description

Cinnamaldehyde diethyl acetal is a chemical compound with a sweet, fruity, and slightly floral aroma, often used in the fragrance and flavor industries. It is classified as an aldehyde, and its primary use is as a flavoring agent and fragrance in various products such as perfumes, soaps, and foods. The compound is typically produced through a reaction between cinnamaldehyde and ethanol, resulting in a colorless to pale yellow liquid with a highly potent odor. Overall, cinnamaldehyde diethyl acetal is widely utilized for its pleasant scent and taste-enhancing properties in consumer products.

Check Digit Verification of cas no

The CAS Registry Mumber 7148-78-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7148-78:
(6*7)+(5*1)+(4*4)+(3*8)+(2*7)+(1*8)=109
109 % 10 = 9
So 7148-78-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H18O2/c1-3-14-13(15-4-2)11-10-12-8-6-5-7-9-12/h5-11,13H,3-4H2,1-2H3

7148-78-9SDS

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 CINNAMALDEHYDE DIETHYL ACETAL

1.2 Other means of identification

Product number -
Other names Zimtaldehyd-diaethylacetal

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:7148-78-9 SDS

7148-78-9Relevant articles and documents

ALLOSTERIC MODULATORS OF NICOTINIC ACETYLCHOLINE RECEPTORS

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Paragraph 0554, (2017/10/13)

The present disclosure relates to compounds of formula I that are useful as modulators of α7 nAChR, compositions comprising such compounds, and the use of such compounds for preventing, treating, or ameliorating disease, particularly disorders of the central nervous system such as cognitive impairments in Alzheimer's disease, Parkinson's disease, and schizophrenia, as well as for L-DOPA induced-dyskinesia and inflammation

Facile synthesis of Cu3(BTC)2/cellulose acetate mixed matrix membranes and their catalytic applications in continuous flow process

Hou, Junying,Luan, Yi,Huang, Xiubing,Gao, Hongyi,Yang, Mu,Lu, Yunfeng

, p. 9123 - 9129 (2017/08/29)

Metal-organic framework (MOF)-based mixed matrix membranes (MMMs) were fabricated by a combination of Cu3(BTC)2 MOF and polymer cellulose acetate. The cellulose acetate in the MMMs served as the matrix and the Cu3(BTC)2 MOF as the filler. The as-synthesized MMMs were utilized as a heterogeneous catalyst for aldehyde acetalization. The characterization techniques indicated that the Cu3(BTC)2 crystals were uniformly dispersed in the MMMs. The BET surface area of the Cu3(BTC)2-based MMM was measured to be 459 m2 g-1 at 60 wt% Cu3(BTC)2 loading. Furthermore, the MMMs served as an excellent catalyst under our continuous flow catalytic reaction conditions. The optimal catalytic result of benzaldehyde yield reached 94% with 60 wt% Cu3(BTC)2 loading of the MMMs at room temperature and the benzaldehyde diethyl acetal reached 0.59 mmol min-1 gCu-BTC-1.

Ferric hydroxide supported gold subnano clusters or quantum dots: Enhanced catalytic performance in chemoselective hydrogenation

Liu, Lequan,Qiao, Botao,Ma, Yubo,Zhang, Juan,Deng, Youquan

, p. 2542 - 2548 (2008/09/20)

An attempt to prepare ferric hydroxide supported Au subnano clusters via modified co-precipitation without any calcination was made. High resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) have been employed to study the structure and chemical states of these catalysts. No Au species could be observed in the HRTEM image nor from the XRD pattern, suggesting that the sizes of the Au species in and on the ferric hydroxide support were less than or around 1 nm. Chemoselective hydrogenation of aromatic nitro compounds and α,β-unsaturated aldehydes was selected as a probe reaction to examine the catalytic properties of this catalyst. Under the same reaction conditions, such as 100 °C and 1 MPa H2 in the hydrogenation of aromatic nitro compounds, a 96-99% conversion (except for 4-nitrobenzonitrile) with 99% selectivity was obtained over the ferric hydroxide supported Au catalyst, and the TOF values were 2-6 times higher than that of the corresponding ferric oxide supported catalyst with 3-5 nm size Au particles. For further evaluation of this Au catalyst in the hydrogenation of citral and cinnamaldehyde, selectivity towards unsaturated alcohols was 2-20 times higher than that of the corresponding ferric oxide Au catalyst. The Royal Society of Chemistry.

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