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4-(4-chlorophenyl)-3-phenylbut-3-en-2-ol is a complex organic compound with the molecular formula C20H17ClO. It is a derivative of but-3-en-2-ol, featuring a 4-chlorophenyl group attached to the 4th carbon and a phenyl group attached to the 3rd carbon. This molecule is characterized by its unique structure, which includes a conjugated diene system and a hydroxyl group, making it a potential intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its chemical properties and reactivity are influenced by the presence of the chlorine atom and the aromatic rings, which can participate in various chemical reactions such as substitution, addition, and elimination. The compound's specific applications and properties would depend on the context in which it is used, and further research would be required to explore its potential uses and effects.

6273-41-2

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6273-41-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6273-41-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6273-41:
(6*6)+(5*2)+(4*7)+(3*3)+(2*4)+(1*1)=92
92 % 10 = 2
So 6273-41-2 is a valid CAS Registry Number.

6273-41-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-chlorophenyl)-3-phenylbut-3-en-2-ol

1.2 Other means of identification

Product number -
Other names -

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:6273-41-2 SDS

6273-41-2Downstream Products

6273-41-2Relevant academic research and scientific papers

Iridium-catalyzed asymmetric hydrogenation of α-substituted α,β-unsaturated acyclic ketones: Enantioselective total synthesis of (-)-mesembrine

Zhang, Qian-Qian,Xie, Jian-Hua,Yang, Xiao-Hui,Xie, Jian-Bo,Zhou, Qi-Lin

supporting information, p. 6158 - 6161 (2013/02/23)

A highly efficient asymmetric hydrogenation of α-substituted α,β-unsaturated acyclic ketones catalyzed by chiral spiro iridium complexes for the preparation of chiral 2-substituted allylic alcohols has been developed (ee up to 99.7%). This method provides a concise route to (-)-mesembrine (34% yield, 12 steps).

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