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173031-63-5

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173031-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 173031-63-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,0,3 and 1 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 173031-63:
(8*1)+(7*7)+(6*3)+(5*0)+(4*3)+(3*1)+(2*6)+(1*3)=105
105 % 10 = 5
So 173031-63-5 is a valid CAS Registry Number.

173031-63-5Downstream Products

173031-63-5Relevant articles and documents

Chiral Carbanions, 1. - Configurational Stability and Reactions of α-Acyloxy-Substituted α-Methylbenzyllithium Compounds

Hammerschmidt, Friedrich,Hanninger, Achim

, p. 1069 - 1078 (2007/10/03)

Racemic and optically active 1-phenylethyl esters of pivalic, (-)-camphanic and 2,4,6-triisopropylbenzoic acid were prepared.The esters 7a of pivalic acid were deprotonated with lithium 2,2,6,6-tetramethylpiperidide (Li-TMP) to form α-oxy-α-methylbenzyllithium compounds which are partly configurationally stable prior to acylation with starting material.Camphanic ester (-)-7b cannot be deprotonated by Li-TMP and t-BuLi is added to the ester function to afford ketone (-)-12a. 1-Phenylethyl 2,4,6-triisopropylbenzoates 16 were transformed within minutes to carbanions 19 by using s-BuLi/TMEDA in THF, hexane, toluene and s-BuLi without TMEDA in toluene/20percent diethyl ether at -78 deg C.The carbanions are configurationally stable only in toluene/20percent diethyl ether and racemise partly in the other solvents.They react with a variety of electrophiles with either retention or inversion (Me3SnCl) of configuration.Carbanions 19 rearrange on warming to -20 deg C to hydroxy ketone 24 with racemisation. - Keywords: Esters, 1-phenylethyl; Carbanions, α-methyl-α-oxybenzyl, configurational stability; Ester-hydroxy ketone rearrangement

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