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benzoic acid 3-cyclohexylidene-allyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1204342-30-2

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1204342-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1204342-30-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,4,3,4 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1204342-30:
(9*1)+(8*2)+(7*0)+(6*4)+(5*3)+(4*4)+(3*2)+(2*3)+(1*0)=92
92 % 10 = 2
So 1204342-30-2 is a valid CAS Registry Number.

1204342-30-2Relevant academic research and scientific papers

Synthesis of Functionalized [3], [4], [5] and [6]Dendralenes through Palladium-Catalyzed Cross-Couplings of Substituted Allenoates

Lippincott, Daniel J.,Linstadt, Roscoe T. H.,Maser, Michael R.,Lipshutz, Bruce H.

, p. 847 - 850 (2017/01/14)

A mild method for the synthesis of highly functionalized [3]–[6]dendralenes is reported, representing a general strategy to diversely substituted higher homologues of the dendralenes. The methodology utilizes allenoates bearing various substitution patter

Asymmetric gold-catalyzed lactonizations in water at room temperature

Handa, Sachin,Lippincott, Daniel J.,Aue, Donald H.,Lipshutz, Bruce H.

, p. 10658 - 10662 (2015/05/13)

Asymmetric gold-catalyzed hydrocarboxylations are reported that show broad substrate scope. The hydrophobic effect associated with in situ-formed aqueous nanomicelles gives good to excellent ee's of product lactones. In-flask product isolation, along with

Unusual regiodivergence in metal-catalysed intramolecular cyclisation of γ-allenols

Arbour, Jannine L.,Rzepa, Henry S.,White, Andrew J. P.,Hii, King Kuok

supporting information; experimental part, p. 7125 - 7127 (2010/03/25)

Different O-heterocycles can be obtained from a common γ-allenol precursor by using Ag, Zn or Sn catalysts; the results were rationalised by molecular modelling. The Royal Society of Chemistry 2009.

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