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38447-05-1

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38447-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38447-05-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,4 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 38447-05:
(7*3)+(6*8)+(5*4)+(4*4)+(3*7)+(2*0)+(1*5)=131
131 % 10 = 1
So 38447-05-1 is a valid CAS Registry Number.

38447-05-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-phenyl-(2E,4E)-pentadienoic acid methyl ester

1.2 Other means of identification

Product number -
Other names methyl (E,E)-5-phenylpenta-2,4-dien-1-oate

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:38447-05-1 SDS

38447-05-1Relevant articles and documents

Visible Light Induced Br?nsted Acid Assisted Pd-Catalyzed Alkyl Heck Reaction of Diazo Compounds and N-Tosylhydrazones

Dubrovina, Anastasiia,Gevorgyan, Vladimir,Kvasovs, Nikita,Zhang, Ziyan

, (2021/11/30)

A mild visible light-induced palladium-catalyzed alkyl Heck reaction of diazo compounds and N-tosylhydrazones is reported. A broad range of vinyl arenes and heteroarenes with high functional group tolerance, as well as a range of different diazo compounds, can efficiently undergo this transformation. This method features Br?nsted acid-assisted generation of hybrid palladium C(sp3)-centered radical intermediate, which allowed for new selective C?H functionalization protocol.

Ruthenium-Catalyzed Oxidative Cross-Coupling Reaction of Activated Olefins with Vinyl Boronates for the Synthesis of (E, E)-1,3-Dienes

Dethe, Dattatraya H.,Beeralingappa, Nagabhushana C.,Uike, Amar

, p. 3444 - 3455 (2021/02/16)

An oxidative cross-coupling reaction between activated olefins and vinyl boronate derivatives has been developed for the highly stereoselective construction of synthetically useful (E,E)-1,3-dienes. The highlight of this reaction is that exclusive stereoselectivity (only E,E-isomer) was achieved from a base-free, ligand-free, and mild catalytic condition with a less expensive [RuCl2(p-cymene)]2 catalyst.

Hydroperoxidations of Alkenes using Cobalt Picolinate Catalysts

Peralta-Neel, Zulema,Woerpel

supporting information, p. 5002 - 5006 (2021/06/30)

Hydroperoxides were synthesized in one step from various alkenes using Co(pic)2as the catalyst with molecular oxygen and tetramethyldisiloxane (TMDSO). The hydration product could be obtained using a modified catalyst, Co(3-mepic)2, with molecular oxygen and phenylsilane. Formation of hydroperoxides occurred through a rapid Co-O bond metathesis of a peroxycobalt compound with isopropanol.

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