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39806-16-1

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39806-16-1 Usage

Synthesis Reference(s)

Tetrahedron Letters, 32, p. 513, 1991 DOI: 10.1016/S0040-4039(00)79482-2

Check Digit Verification of cas no

The CAS Registry Mumber 39806-16-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,8,0 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 39806-16:
(7*3)+(6*9)+(5*8)+(4*0)+(3*6)+(2*1)+(1*6)=141
141 % 10 = 1
So 39806-16-1 is a valid CAS Registry Number.

39806-16-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 5-phenylpenta-2,4-dienoate

1.2 Other means of identification

Product number -
Other names ethyl 5-phenyl-2,4-pentadienoate

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:39806-16-1 SDS

39806-16-1Relevant articles and documents

PREPARATION AND RESOLUTION OF (η4-1,3-DIENECARBOXYLIC ACID)Fe(CO)3 COMPLEXES

Nakanishi, Saburo,Kumeta, Katsuhisa,Nakanishi, Jun-Ichi,Takata, Toshikazu

, p. 2097 - 2100 (1995)

(η4-1,3-dienecarboxylic acid)Fe(CO)3 complexes 1 were prepared starting from a Horner-Emmons reaction of α,β-unsaturated aldehydes, followed by complexation with Fe(CO)5 and hydrolysis of the ester groups.Reaction of 1 with (S)-2-octanol gave a

Cobalt-Catalyzed Diastereo- And Enantioselective Reductive Allyl Additions to Aldehydes with Allylic Alcohol Derivatives via Allyl Radical Intermediates

Wang, Lei,Wang, Lifan,Li, Mingxia,Chong, Qinglei,Meng, Fanke

supporting information, p. 12755 - 12765 (2021/08/30)

Catalytic generation of ambiphilic π-allyl-metal complexes and their utility in enantioselective transformations constitutes a powerful approach for introduction of allyl groups to a molecule. Herein an unprecedented cobalt-catalyzed highly site-, diastereo-, and enantioselective protocol for stereoselective formation of nucleophilic allyl-Co(II) complexes followed by addition to aldehydes is presented. The reaction features diastereo- and enantioconvergent conversion of easily accessible allylic alcohol derivatives to diversified enantioenriched homoallylic alcohols with a remarkably broad scope of allyl groups that can be introduced. Mechanistic studies indicated that allyl radical intermediates were involved in this process. These new discoveries establish a new strategy for development of enantioselective transformations through capture of radicals by chiral Co complexes, pushing forward the frontier of Co complexes for enantioselective catalysis.

Systematic Study on the Catalytic Arsa-Wittig Reaction

Inaba, Ryoto,Kawashima, Ikuo,Fujii, Toshiki,Yumura, Takashi,Imoto, Hiroaki,Naka, Kensuke

supporting information, p. 13400 - 13407 (2020/09/21)

Efficient catalytic arsa-Wittig reactions have been developed by using 1-phenylarsolane as a catalyst. A wide array of aldehydes was converted to the corresponding olefins in high yields with moderate to excellent E stereoselectivity in the presence of a catalytic amount of 1-phenylarsolane. Moreover, density functional theory calculations were carried out to afford insight into the E/Z selectivity.

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