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1-Acetyl-2-[1-(2-naphthyl)ethyl]benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1246820-30-3

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1246820-30-3 Usage

Type of compound

Chemical compound

Derivative of

Benzene

Attached groups

Naphthyl group and an acetyl group

Usage

a. Organic synthesis
b. Reagent
c. Building block for pharmaceuticals and biologically active molecules
d. Starting material for dyes, fragrances, and industrial chemicals

Physical state at room temperature

Solid

Solubility

Soluble in organic solvents such as ether, acetone, and toluene

Safety precautions

a. Harmful if swallowed
b. Harmful if inhaled
c. Harmful if in contact with skin
d. Harmful if in contact with eyes

Check Digit Verification of cas no

The CAS Registry Mumber 1246820-30-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,6,8,2 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1246820-30:
(9*1)+(8*2)+(7*4)+(6*6)+(5*8)+(4*2)+(3*0)+(2*3)+(1*0)=143
143 % 10 = 3
So 1246820-30-3 is a valid CAS Registry Number.

1246820-30-3Downstream Products

1246820-30-3Relevant academic research and scientific papers

Cobalt-catalyzed branched-selective addition of aromatic ketimines to styrenes under room-temperature conditions

Dong, Jinghua,Lee, Pin-Sheng,Yoshikai, Naohiko

supporting information, p. 1140 - 1142 (2013/10/22)

An improved cobalt-based catalytic system has been developed for the branched-selective addition of aromatic ketimines to styrenes. With an appropriate combination of triarylphosphine and the Grignard reagent, the reaction takes place smoothly at room temperature to afford 1,1-diarylethane derivatives with high regioselectivity.

Regioselectivity-switchable hydroarylation of styrenes

Gao, Ke,Yoshikai, Naohiko

supporting information; experimental part, p. 400 - 402 (2011/04/16)

Cobalt-phosphine and cobalt-carbene catalysts have been developed for the hydroarylation of styrenes via chelationassisted C-H bond activation, to afford branched and linear addition products, respectively, in a highly regioselective fashion. Deuterium-la

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