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3-(prop-2-en-1-yl)-4-(prop-2-en-1-yloxy)benzaldehyde is a complex organic compound with the molecular formula C14H14O2. It is characterized by a benzaldehyde structure, which includes a benzene ring with a formyl group (CHO) attached to it. The compound features two prop-2-en-1-yl (allyl) groups, one attached to the 3rd carbon of the benzene ring and the other as an ether group (-O-) attached to the 4th carbon. This chemical is known for its aromatic properties and is used in the synthesis of various pharmaceuticals and fragrances due to its unique structure and reactivity. It is an important intermediate in organic chemistry, particularly in the preparation of compounds with potential applications in the chemical and pharmaceutical industries.

136433-45-9

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136433-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136433-45-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,4,3 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 136433-45:
(8*1)+(7*3)+(6*6)+(5*4)+(4*3)+(3*3)+(2*4)+(1*5)=119
119 % 10 = 9
So 136433-45-9 is a valid CAS Registry Number.

136433-45-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-prop-2-enoxy-3-prop-2-enylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 3-Allyl-4-allyloxy-benzaldehyd

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:136433-45-9 SDS

136433-45-9Relevant academic research and scientific papers

Allylphenols as a new class of human 15-lipoxygenase-1 inhibitors

Alavi, Seyed Jamal,Seyedi, Seyed Mohammad,Saberi, Satar,Safdari, Hadi,Eshghi, Hossein,Sadeghian, Hamid

, p. 259 - 266 (2020/10/12)

In this study, a series of mono- and diallylphenol derivative were designed, synthesized, and evaluated as potential human 15-lipoxygenase-1 (15-hLOX-1) inhibitors. Radical scavenging potency of the synthetic allylphenol derivatives was assessed and the results were in accordance with lipoxygenase (LOX) inhibition potency. It was found that the electronic natures of allyl moiety and para substituents play the main role in radical scavenging activity and subsequently LOX inhibition potency of the synthetic inhibitors. Among the synthetic compounds, 2,6-diallyl-4-(hexyloxy)phenol (42) and 2,6-diallyl-4-aminophenol (47) showed the best results for LOX inhibition (IC50 = 0.88 and 0.80 μM, respectively).

Synthesis of 1-indanonyl oxepanes

Chang, Meng-Yang,Lee, Nien-Chia

, p. 867 - 872 (2012/06/01)

A variety of 1-indanonyl oxepanes with the novel structure of indanonyl oxepanes was prepared from reaction of hydroxybenzaldehydes via a series of reasonable transformations, including the regioselective PhBClmediated allylation (or Claisen rearrangement), one-pot reaction of ring-closing metathesis and the Wittig olefination, hydrogenation, and the Friedel-Crafts intramolecular cyclization. Georg Thieme Verlag Stuttgart . New York.

An isomerization-ring-closing metathesis strategy for the synthesis of substituted benzofurans

Van Otterlo, Willem A.L.,Morgans, Garreth L.,Madeley, Lee G.,Kuzvidza, Samuel,Moleele, Simon S.,Thornton, Natalie,De Koning, Charles B.

, p. 7746 - 7755 (2007/10/03)

Twelve substituted benzofurans were synthesized from their corresponding substituted 1-allyl-2-allyloxybenzenes using ruthenium-mediated C- and O-allyl isomerization followed by ring-closing metathesis.

Aryl-substituted rhodanine derivatives

-

, (2008/06/13)

Provided are certain aryl-substituted rhodanine derivatives, treatment methods and pharmaceutical formulations thereof.

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