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3-(Biphenyl-3-yl)cyclohex-2-en-1-one is an organic compound characterized by a unique molecular structure. It features a cyclohexenone ring, which is a six-membered carbon ring with a double bond and a ketone group. Attached to this ring is a biphenyl group, which consists of two benzene rings bonded together. 3-(biphenyl-3-yl)cyclohex-2-en-1-one is known for its potential applications in the synthesis of various pharmaceuticals and chemical compounds due to its complex structure and reactivity. It is typically synthesized through organic chemistry methods and is used as an intermediate in the production of more complex molecules. The compound's properties, such as its reactivity and stability, make it a valuable component in advanced chemical research and development.

6301-52-6

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6301-52-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6301-52-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6301-52:
(6*6)+(5*3)+(4*0)+(3*1)+(2*5)+(1*2)=66
66 % 10 = 6
So 6301-52-6 is a valid CAS Registry Number.

6301-52-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3-phenylphenyl)cyclohex-2-en-1-one

1.2 Other means of identification

Product number -
Other names 3-<Biphenyl-3-yl>-cyclohex-2-enon

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:6301-52-6 SDS

6301-52-6Relevant academic research and scientific papers

Chemoselective three-component coupling via a tandem Pd-catalyzed boron-Heck and Suzuki reactions

O'Neill, Justin,Yoo, Kyung Soo,Jung, Kyung Woon

supporting information; experimental part, p. 7307 - 7310 (2009/04/14)

A new approach is herein reported to prepare biaryl derivatives via a tandem Pd-catalyzed boron-Heck and Suzuki reactions. This one-pot tandem process avoided purification or addition of extra catalyst between steps. The resulting biaryl compounds can be

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