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3-Buten-2-one, 1-cyclohexyl-4-phenyl-, also known as 1-cyclohexyl-4-phenylbut-3-en-2-one, is an organic compound with the molecular formula C16H18O. It is a colorless to pale yellow liquid with a molecular weight of 226.31 g/mol. 3-Buten-2-one, 1-cyclohexyl-4-phenyl- is characterized by the presence of a buten-2-one functional group, a cyclohexyl group, and a phenyl group. It is used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its complex structure, it is typically synthesized through multi-step reactions involving the use of various reagents and catalysts. The compound is sensitive to light and heat, and should be stored in a cool, dry place away from direct sunlight.

1760-54-9

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1760-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1760-54-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,6 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1760-54:
(6*1)+(5*7)+(4*6)+(3*0)+(2*5)+(1*4)=79
79 % 10 = 9
So 1760-54-9 is a valid CAS Registry Number.

1760-54-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclohexyl-4-phenylbut-3-en-2-one

1.2 Other means of identification

Product number -
Other names 3-Buten-2-one,1-cyclohexyl-4-phenyl

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1760-54-9 SDS

1760-54-9Upstream product

1760-54-9Relevant academic research and scientific papers

Stereodivergent Additions of Allylic Chromium(III) Reagents to Aldehydes

Jubert, Carole,Nowotny, Stefan,Kornemann, Dirk,Antes, Iris,Tucker, Charles E.,Knochel, Paul

, p. 6384 - 6386 (1992)

In contrast to γ-monosubstituted allylic chromium reagents, γ-disubstituted allylic chromium(III) organometallics undergo highly stereoselective stereodivergent additions to aldehydes.

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