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(S)-4-methyl-1-phenyl-2-pentanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

736143-84-3

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736143-84-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 736143-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,3,6,1,4 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 736143-84:
(8*7)+(7*3)+(6*6)+(5*1)+(4*4)+(3*3)+(2*8)+(1*4)=163
163 % 10 = 3
So 736143-84-3 is a valid CAS Registry Number.

736143-84-3Relevant academic research and scientific papers

Catalytic conjunctive cross-coupling enabled by metal-induced metallate rearrangement

Zhang, Liang,Lovinger, Gabriel J.,Edelstein, Emma K.,Szymaniak, Adam A.,Chierchia, Matteo P.,Morken, James P.

, p. 70 - 74 (2016/01/09)

Transition metal catalysis plays a central role in contemporary organic synthesis. Considering the tremendously broad array of transition metal-catalyzed transformations, it is remarkable that the underlying elementary reaction steps are relatively few in

Screening on the use of Kluyveromyces marxianus CBS 6556 growing cells as enantioselective biocatalysts for ketone reductions

Vitale, Paola,Perna, Filippo Maria,Perrone, Maria Grazia,Scilimati, Antonio

experimental part, p. 1985 - 1993 (2012/03/22)

The versatility of Kluyveromyces marxianus CBS 6556 growing cells in the enantioselective reduction of ketone functionalities to the corresponding alcohols was exploited. In particular, methyl ketones were reduced to (S)-alcohols with ees of up to 96%. Longer chain alkyl ketones afforded, under the same experimental condition, (R)-alcohols with an ee of up to 84%. Interestingly, carbon-carbon double and the triple bonds can also be reduced in the presence of Kluyveromyces marxianus CBS 6556 yeast. A cyclic ketone, such as 2-tetralone, was also quantitatively reduced to its corresponding (S)-alcohol with ee = 76%.

Preparation of enantiomerically enriched flavor and fragrance components

-

, (2008/06/13)

The present invention includes a process for enantioselective preparation of a non-racemic compound, which is either usable as a fragrance or flavor component or is convertible to a fragrance or flavor component by one or more additional reaction steps. T

Chiral vinyl dioxazaborocines in synthesis: Asymmetric cuprate additions to β-boronyl acrylates and vinyl sulfones

Farthing, Christopher N.,Marsden, Stephen P.

, p. 4235 - 4238 (2007/10/03)

The first examples of the addition of organometallic reagents to electron deficient boron-substituted olefins are reported. Thus, copper catalysed addition of Grignard reagents to chiral acryloyl and vinysulfonyl dioxazaborocines, followed by oxidative re

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