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2463-63-0

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2463-63-0 Usage

Description

2-Heptenal has a pungent green somewhat fatty odor, pleasant only on extreme dilution. May be prepared by oxidation of butylallyl alcohol.

Chemical Properties

2-Heptenal has a pungent green somewhat fatty odor, pleasant only on extreme dilution.

Occurrence

Reported found in soybean oil, potato chips, cranberry, raisin, strawberry, asparagus, peas, tomato, Russian cheeses, butter, caviar, fatty fsh, roasted turkey, cooked beef, cured pork, pork fat and liver, cognac, flberts, pecans, peanuts, soy- bean, beans, mango, walnut, unprocessed rice, malt, wort and lingonberry

Definition

ChEBI: An enal consisting of hept-2-ene having an oxo group at the 1-position.

Preparation

By oxidation of butylallyl alcohol.

Aroma threshold values

Detection: 13 to 51 ppb.

Taste threshold values

Taste characteristics at 4 ppm: intense green, sweet, fresh fruity apple-skin nuances.

Check Digit Verification of cas no

The CAS Registry Mumber 2463-63-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,6 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2463-63:
(6*2)+(5*4)+(4*6)+(3*3)+(2*6)+(1*3)=80
80 % 10 = 0
So 2463-63-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O/c1-2-3-4-5-6-7-8/h5-7H,2-4H2,1H3/b6-5-

2463-63-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name hept-2-enal

1.2 Other means of identification

Product number -
Other names trans-2-Hepten-1-ol,remainder mainly cis-isomer

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:2463-63-0 SDS

2463-63-0Relevant articles and documents

Enhancing the photo-efficacy of an organic visible-light-activated chromophore (alizarin red S) on zinc oxide with a Ag-Na electrolyte to photo-transform aromatic and aliphatic alcohols

Underwood, Timothy M.,Robinson, Ross S.

, p. 24259 - 24266 (2019)

The development of an aqueous silver-sodium/alizarin red sensitised zinc oxide system has been reported to oxidise a range of both aromatic and aliphatic alcohols to aldehydes. Furthermore, photoluminescence spectroscopy validated the electron quenching effect of zinc oxide's defect sites after surface sensitising the metal-oxide with alizarin red. Powder diffuse reflectance UV/Vis data further substantiated the visible-light attenuated properties of alizarin red sensitised zinc oxide, and hence justification for its visible light reactivity towards alcohol oxidations. Lastly, density functional theory calculations supported the intermolecular photo-electronic transfer between alizarin red organic and zinc oxide.

Enantioselective Organocatalytic Synthesis of 1,2,3-Trisubstituted Cyclopentanes

?otolová, Martina,Kamlar, Martin,Reme?, Marek,Géant, Pierre-Yves,Císa?ová, Ivana,?tícha, Martin,Vesely, Jan

, p. 5080 - 5089 (2021/09/30)

An organocatalytic asymmetric domino Michael/α-alkylation reaction between enals and non-stabilized alkyl halides has been developed. Chiral secondary amine catalyzed cyclization reaction of 1-bromo-3-nitropropane with α,β-unsaturated aldehydes provides 1,2,3-trisubstituted cyclopentane carbaldehydes with high diastereo- (dr up to 8 : 1) and enantioselectivities (ee up to 96 %).

Combined heterogeneous metal/chiral amine: Multiple relay catalysis for versatile eco-friendly synthesis

Deiana, Luca,Jiang, Yan,Palo-Nieto, Carlos,Afewerki, Samson,Incerti-Pradillos, Celia A.,Verho, Oscar,Tai, Cheuk-Wai,Johnston, Eric V.,C?rdova, Armando

supporting information, p. 3447 - 3451 (2014/04/03)

Herein is described a versatile and broad synergistic strategy for expansion of chemical space and the synthesis of valuable molecules (e.g. carbocycles and heterocycles), with up to three quaternary stereocenters, in a highly enantioselective fashion from simple alcohols (31 examples, 95:5 to >99.5:0.5 e.r.) using integrated heterogeneous metal/chiral amine multiple relay catalysis and air/O2 as the terminal oxidant. A novel highly 1,4-selective heterogeneous metal/amine co-catalyzed hydrogenation of enals was also added to the relay catalysis sequences. Relay switch: A versatile strategy for expansion of chemical space and the synthesis of valuable molecules, having up to three quaternary stereocenters, in a highly enantioselective fashion from simple alcohols is described. The method employs integrated heterogeneous metal/chiral amine multiple relay catalysis and air/O2 as the terminal oxidant.

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