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2-[(4-methylphenyl)methylene]heptan-1-al

  • CAS:84697-09-6
  • purity:99%
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Top Quality 2-[(4-methylphenyl)methylene]heptan-1-al 84697-09-6 Hot Sell In Stock

  • Molecular Formula: C15H20O
  • Molecular Weight: 216.323
  • Vapor Pressure: 0.000101mmHg at 25°C 
  • Refractive Index: 1.532 
  • Boiling Point: 338 °C at 760 mmHg 
  • Flash Point: 141.4 °C 
  • Density: 0.955 g/cm3 

2-[(4-methylphenyl)methylene]heptan-1-al(Cas 84697-09-6) Usage

General Description

2-[(4-methylphenyl)methylene]heptan-1-al, also known as p-Methylcinnamaldehyde, is a chemical compound commonly used in the fragrance industry. It is a colorless to pale yellow liquid with a sweet, floral, and woody odor. 2-[(4-methylphenyl)methylene]heptan-1-al is often used as a fragrance ingredient in perfumes, soaps, and cosmetics, as well as in the production of flavorings for food and beverages. Its aromatic and versatile nature makes it a popular choice for adding a warm, spicy, and slightly fruity aroma to various consumer products. Additionally, it is also used in the synthesis of pharmaceutical compounds and as a flavoring agent in the food industry.

InChI:InChI=1/C15H20O/c1-3-4-5-6-15(12-16)11-14-9-7-13(2)8-10-14/h7-12H,3-6H2,1-2H3/b15-11-

84697-09-6 Relevant articles

Oxygenation of Simple Olefins through Selective Allylic C?C Bond Cleavage: A Direct Approach to Cinnamyl Aldehydes

Liu, Jianzhong,Wen, Xiaojin,Qin, Chong,Li, Xinyao,Luo, Xiao,Sun, Ao,Zhu, Bencong,Song, Song,Jiao, Ning

supporting information, p. 11940 - 11944 (2017/09/20)

A novel metal-free allylic C?C σ-bond cl...

Synthesis of α,β-unsaturated aldehydes based on a one-pot phase-switch dehydrogenative cross-coupling of primary alcohols

Mura, Manuel G.,De Luca, Lidia,Taddei, Maurizio,Williams, Jonathan M. J.,Porcheddu, Andrea

supporting information, p. 2586 - 2589 (2014/06/09)

An efficient one-pot ruthenium-catalyzed...

A new route to α,β-unsaturated aldehydes using the condensation of trimethylsilyl β-trimethylsilyl enol ethers with aldehydes

Duhamel, Lucette

, p. 7745 - 7748 (2007/10/02)

β-Trimethylsilyl enol ethers 1 (Z) obtai...

84697-09-6 Process route

n-heptan1ol
111-70-6

n-heptan1ol

4-Methylbenzyl alcohol
589-18-4

4-Methylbenzyl alcohol

(E)-2-(4-methylbenzylidene)heptanal
84697-09-6

(E)-2-(4-methylbenzylidene)heptanal

Conditions
Conditions Yield
With but-2-enenitrile; carbonyl bis(hydrido)tris(triphenylphosphine)ruthenium(II); 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In neat (no solvent); at 120 ℃; for 3h; chemoselective reaction; Microwave irradiation; Inert atmosphere; Sealed tube;
61%
4-methyl-benzaldehyde
104-87-0

4-methyl-benzaldehyde

(Z)-2-Trimethylsilanyl-1-trimethylsilanyloxy-hept-1-ene
154581-95-0

(Z)-2-Trimethylsilanyl-1-trimethylsilanyloxy-hept-1-ene

(E)-2-(4-methylbenzylidene)heptanal
84697-09-6

(E)-2-(4-methylbenzylidene)heptanal

Conditions
Conditions Yield
trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at 0 ℃; for 4h;
90%

84697-09-6 Upstream products

  • 104-87-0
    104-87-0

    4-methyl-benzaldehyde

  • 154581-95-0
    154581-95-0

    (Z)-2-Trimethylsilanyl-1-trimethylsilanyloxy-hept-1-ene

  • 111-70-6
    111-70-6

    n-heptan1ol

  • 589-18-4
    589-18-4

    4-Methylbenzyl alcohol

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