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25166-87-4

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  • trans-4-hexenaldehyde CAS NO.25166-87-4 CAS NO.25166-87-4

    Cas No: 25166-87-4

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25166-87-4 Usage

Chemical Properties

trans-4-hexenal has a “green” vegetable odor

Aroma threshold values

Detection at 0.0003 ppm in water. Detection and recognition in air at 0.0029 and 0.014 mg/m3, respectively

Check Digit Verification of cas no

The CAS Registry Mumber 25166-87-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,6 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 25166-87:
(7*2)+(6*5)+(5*1)+(4*6)+(3*6)+(2*8)+(1*7)=114
114 % 10 = 4
So 25166-87-4 is a valid CAS Registry Number.

25166-87-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-4-hexenaldehyde

1.2 Other means of identification

Product number -
Other names (E)-4-Hexenal

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:25166-87-4 SDS

25166-87-4Relevant articles and documents

Photocatalytic One-Pot Synthesis of Homoallyl Ketones via a Norrish Type i Reaction of Cyclopentanones

Okada, Megumi,Yamada, Keiichi,Fukuyama, Takahide,Ravelli, Davide,Fagnoni, Maurizio,Ryu, Ilhyong

, p. 9365 - 9369 (2015/09/28)

A photocatalytic synthesis of homoallyl ketones was achieved via a one-pot procedure starting from a Norrish Type I reaction of cyclopentanones, followed by a decatungstate-catalyzed hydroacylation of electron-deficient olefins by the resulting 4-pentenals. The site-selective formyl H-abstraction in the second step can be explained by radical polar effects in the transition state.

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