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2-(Methoxy-phenyl-methyl)-cyclopentanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85670-55-9

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85670-55-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85670-55-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,7 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 85670-55:
(7*8)+(6*5)+(5*6)+(4*7)+(3*0)+(2*5)+(1*5)=159
159 % 10 = 9
So 85670-55-9 is a valid CAS Registry Number.

85670-55-9Downstream Products

85670-55-9Relevant academic research and scientific papers

Stereoselective Cross-Aldol Reactions of Silyl Enol Ethers with Acetals Catalyzed by Iodotrimethylsilane

Sakurai, Hideki,Sasaki, Koshi,Hosomi, Akira

, p. 3195 - 3196 (1983)

Iodotrimethylsilane catalyzes effectively erythroselective aldol type condensation of silyl enol ethers with acetals.

NOUVELLE SYNTHESE REGIOSELECTIVE DE β-ALCOXYCETONES A PARTIR D'ENOXYSILANES ET DE TRISENOXYSILANES ENGENDRES in situ

Rochin, Christophe,Babot, Odile,Duboudin, Francoise

, p. C24 - C28 (2007/10/02)

An easy, regiospecific, route to β-alkoxyketones based on the use of methyl trichlorosilane for in situ generation of α-chloroethers and trisenoxysilanes is described.

TRITYL PERCHLORATE AS AN EFFICIENT CATALYST IN THE ALDOL-TYPE REACTION

Mukaiyama, Teruaki,Kobayashi, Shu,Murakami, Masahiro

, p. 1759 - 1762 (2007/10/02)

In the presence of a catalytic amount of trityl perchlorate, silyl enol ethers and ketene silyl acetals react with acetals and methyl orthoformate to give the corresponding aldol-type addition products in good yields.

REACTIONS OF α-HETEROATOM-SUBSTITUTED ETHERS AND SULFIDES WITH SILYL ENOL ETHERS. CHEMOSELECTIVITY IN THE CLEAVAGE OF HETEROATOM-CARBON BONDS BY IODOTRIMETHYLSILANE AND TRIMETHYLSILYL TRIFLUOROMETHANESULFONATE

Hosomi, Akira,Sakata, Yasuyuki,Sakurai, Hideki

, p. 405 - 408 (2007/10/02)

Reactions of α-heteroatom substituted ethers and related compounds (R1R2CXY; X, Y = RO, RS and Cl) with silyl enol ethers and ketene silyl acetals took place in the presence of iodotrimethylsilane (Ia) and trimethylsilyl triflate (Ib) as a catalyst and factors influencing the activation of the heteroatom by I were examined.

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