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3917-39-3

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3917-39-3 Usage

Chemical Properties

Yellow Oil

Uses

(2E,4E)-β-Ionyliden-ethanol (cas# 3917-39-3) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 3917-39-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,1 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3917-39:
(6*3)+(5*9)+(4*1)+(3*7)+(2*3)+(1*9)=103
103 % 10 = 3
So 3917-39-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H24O/c1-12(9-11-16)7-8-14-13(2)6-5-10-15(14,3)4/h7-9,16H,5-6,10-11H2,1-4H3/b8-7+,12-9+

3917-39-3SDS

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 β-Ionyliden-ethanol

1.2 Other means of identification

Product number -
Other names (2E,4E)-3-methyl-5-(2,6,6-trimethylcyclohexen-1-yl)-2,4-pentadienol

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:3917-39-3 SDS

3917-39-3Relevant articles and documents

INCORPORATION OF α-IONYLIDENE ETHANOL AND α-IONYLIDENE ACETIC ACID INTO ABSCISIC ACID BY CERCOSPORA ROSICOLA

Neill, Steven J.,Horgan, Roger

, p. 2469 - 2472 (1983)

2H-Labelled α-ionylidene ethanol and α-ionylidene acetic acid are converted in high yield to 1'-deoxy-abscisic acid (1'-deoxy-ABA) and abscisic acid (ABA) by Cercospora rosicola.Incorporation of label was confirmed by mass spectrometry.The 2-trans isomers

Agents for use on skin and/or hair containing quadruply substituted cyclohexene compounds

-

Page/Page column 12-13, (2010/11/28)

The invention relates to agents for use on skin or hair, particularly for increasing skin tanning and the synthesis of melanin in skin or hair. The invention contains, in particular, cosmetic or dermatological preparations containing quadruply substituted

Palladium-catalyzed coupling reaction of an enol nonaflate with (vinyl)tributylstannanes and acetylenes: A highly stereoselective synthesis of 8,18-13C2-labeled retinal

Wada, Akimori,Ieki, Yasuhiro,Nakamura, Saeko,Ito, Masayoshi

, p. 1581 - 1588 (2007/10/03)

Here we report that enol nonaflates exhibit higher reactivity than the corresponding enol triflates in palladium-catalyzed cross-coupling reactions with various (vinyl)tributylstannanes and acetylenes. We also highlight the reaction of a vinyl nonaflate,

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