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2-Propen-1-one, 2-(4-methoxyphenyl)-1,3-diphenyl-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94348-31-9

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94348-31-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94348-31-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,3,4 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 94348-31:
(7*9)+(6*4)+(5*3)+(4*4)+(3*8)+(2*3)+(1*1)=149
149 % 10 = 9
So 94348-31-9 is a valid CAS Registry Number.

94348-31-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methoxyphenyl)-1,3-diphenylprop-2-en-1-one

1.2 Other means of identification

Product number -
Other names 2-Propen-1-one,2-(4-methoxyphenyl)-1,3-diphenyl

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:94348-31-9 SDS

94348-31-9Downstream Products

94348-31-9Relevant academic research and scientific papers

Exploratory studies toward a synthesis of flavaglines. A novel access to a highly substituted cyclopentenone intermediate

Basmadjian, Christine,Zhao, Qian,Désaubry, Laurent

, p. 727 - 730 (2015/01/30)

The gold(I)-catalyzed intramolecular siloxycyclization developed by Rhee and collaborators was shown to operate also on alkyl ethers to generate a highly substituted 2-cyclopentenone 8, extending the application of this reaction. Conversion of 8 to known anticancer natural products following a reported strategy was examined.

Structure-Activity Relationship of Estrogens: Receptor Affinity and Estrogen Antagonist Activity of Certain (E)- and (Z)-1,2,3-Triaryl-2-propen-1-ones

Mittal, Shubhra,Durani, Susheel,Kapil, Randhir S.

, p. 492 - 497 (2007/10/02)

(E)- nad (Z)-1,2,3-triphenyl-2-propen-1-ones and some of their phenolic and alkoxy analogues, substituted at the para position in one or more aromatic rings, were synthesized and assigned geometry on the basis on their spectroscopic data.The structure-act

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