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(E)-(S)-2-Methyl-6-phenyl-hex-5-en-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40596-22-3

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40596-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40596-22-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,5,9 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 40596-22:
(7*4)+(6*0)+(5*5)+(4*9)+(3*6)+(2*2)+(1*2)=113
113 % 10 = 3
So 40596-22-3 is a valid CAS Registry Number.

40596-22-3Downstream Products

40596-22-3Relevant academic research and scientific papers

Reaction of allylic-type diindium compounds with electrophiles

Hirashita, Tsunehisa,Arai, Shun,Mitsui, Kazuma,Makino, Hajime,Araki, Shuki

, p. 314 - 315 (2006)

Allylic-type diindium reagents were prepared from 3-bromo-1-iodopropene (1a), 3-bromo-1-iodo-1-phenylpropene (1b), or 2,4-diiodobut-2-en-1-ol (1c) with metallic indium, and their successive coupling with electrophiles was examined. The coupling behavior o

Enantioselective synthesis of α-tri- and α-tetrasubstituted allylsilanes by copper-catalyzed asymmetric allylic substitution of allyl phosphates with silylboronates

Takeda, Momotaro,Shintani, Ryo,Hayashi, Tamio

, p. 5007 - 5017 (2013/07/11)

A copper/N-heterocyclic carbene-catalyzed asymmetric allylic substitution of allyl phosphates with a silylboronate has been developed to give highly enantioenriched allylsilanes. High regioselectivity has been achieved by employing NaOH as the base, and this catalyst system is effective for both γ-mono- and disubstituted allyl phosphates.

Enantioselective Allylation of Aldehydes with an Optically Active Allylsilane

Hayashi, Tamio,Konishi, Mitsuo,Kumada, Makoto

, p. 281 - 282 (2007/10/02)

Reaction of aldehydes with an optically active allylsilane, (R)-3-phenyl-3-(trimethylsilyl)propene, in the presence of titanium chloride has been found to proceed with high enantioselectivity to produce optically active homoallylic alcohols of up to 91per

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