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1-((1E,3E)-hexa-1,3,5-trien-1-yl)-4-methoxybenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1434057-97-2

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1434057-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1434057-97-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,4,0,5 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1434057-97:
(9*1)+(8*4)+(7*3)+(6*4)+(5*0)+(4*5)+(3*7)+(2*9)+(1*7)=152
152 % 10 = 2
So 1434057-97-2 is a valid CAS Registry Number.

1434057-97-2Downstream Products

1434057-97-2Relevant academic research and scientific papers

Palladium-Catalyzed Chemoselective Protodecarboxylation of Polyenoic Acids

Al-Huniti, Mohammed H.,Perez, Mark A.,Garr, Matthew K.,Croatt, Mitchell P.

supporting information, p. 7375 - 7379 (2019/01/03)

Conditions for the first palladium-catalyzed chemoselective protodecarboxylation of polyenoic acids to give the desired polyenes in good yields are presented. The reactions proceed under mild conditions using either a Pd(0) or Pd(II) catalyst and tolerate a variety of aryl and aliphatic substitutions. Unique aspects of the reaction include the requirement of phosphines, water, and a polyene adjacent to the carboxylic acid.

Scope and limitations of 1,3,5-hexatriene derivatives in regioselective cobalt-catalyzed reactions

Schmidt, Anastasia,Hilt, Gerhard

supporting information, p. 2708 - 2711 (2013/07/26)

Applications of 1,3,5-hexatriene derivatives in atom-economic cobalt-catalyzed transformations, such as the Diels-Alder reaction with alkynes, the 1,4-hydrovinylation reaction with terminal alkenes, and the 1,4-hydrohexatrienylation reaction, are investigated. In all cases, regioselective transformations were found to generate cyclic derivatives such as stilbenes or acyclic products with a high control of the double bond geometry in the skipped trienes derived from the 1,4-hydrovinylation process or the tetraenes generated in the so far unprecedented 1,4-hydrohexatrienylation reaction.

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