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2-(2-furylmethylene)heptan-1-al, also known as furfuryl heptanal, is a chemical compound belonging to the furan aldehydes family, characterized by its molecular formula C14H18O2. It is recognized for its sweet, hay-like odor and is valued for its aromatic properties in various industries.

67801-21-2

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67801-21-2 Usage

Uses

Used in Food Industry:
2-(2-furylmethylene)heptan-1-al is used as a flavoring agent for adding a nutty and caramel-like aroma to various food products, enhancing their sensory appeal.
Used in Fragrance Industry:
In the fragrance industry, 2-(2-furylmethylene)heptan-1-al is utilized to create warm and woody notes in perfumes and colognes, contributing to the complexity and richness of scents.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, 2-(2-furylmethylene)heptan-1-al may have potential applications in the pharmaceutical industry, possibly due to its chemical properties that could be harnessed for medicinal purposes.
Used as a Chemical Intermediate in Organic Synthesis:
2-(2-furylmethylene)heptan-1-al also serves as a chemical intermediate in organic synthesis, indicating its role in the production of other chemical compounds for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 67801-21-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,8,0 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67801-21:
(7*6)+(6*7)+(5*8)+(4*0)+(3*1)+(2*2)+(1*1)=132
132 % 10 = 2
So 67801-21-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H16O2/c1-2-3-4-6-11(10-13)9-12-7-5-8-14-12/h5,7-10H,2-4,6H2,1H3/b11-9+

67801-21-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3ξ-[2]furyl-2-pentyl-acrylaldehyde

1.2 Other means of identification

Product number -
Other names 2-[1-Furan-2-yl-meth-(Z)-ylidene]-heptanal

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:67801-21-2 SDS

67801-21-2Downstream Products

67801-21-2Relevant academic research and scientific papers

Acid Catalysts Based on Mesoporous Aromatic Frameworks in Aldol Condensation of Furfural with Some Carbonyl Compounds

Talanova, M. Yu.,Yarchak,Karakhanov

, p. 857 - 864 (2019/08/12)

Aldol condensation of furfural with acetone and a series of aldehydes in the presence of PAF-SO3H acid catalyst based on mesoporous aromatic frameworks was investigated. The reaction course depending on the process temperature, catalyst amount, and reactant ratio was considered for the furfural condensation with acetone as an example. The catalyst can be reused in several cycles without appreciable activity loss.

Highly selective aldol condensation using amine-functionalized SiO2-Al2O3 mixed-oxide under solvent-free condition

Abbaspourrad, Alireza,Javad Kalbasi, Roozbeh,Zamani, Farzad

experimental part, p. 2074 - 2082 (2011/06/19)

A series of amine catalysts supported on mesoporous molecular sieves SiO2/Al2O3 with trimethoxysilylpropylamine [(CH3O)3Si(CH2)3NH2] loading varying from 3 mmol to 6 mmol were synthesized by impregnation method. The aldol condensation of various aromatic aldehydes and 1-heptanal was used to test the acid-base cooperativity of amine-functionalized SiO2/Al2O3. The effects of solvent, reaction temperature, benzaldehyde to 1-heptanal molar ratio, different supports (SiO2, Al2O3 and SiO2-Al2O3), catalyst amount and recyclability of the catalyst were investigated. Sample containing 5 mmol amine loaded showed highest benzaldehyde conversion (100%) and selectivity (97%) for jasminaldehyde.

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