Welcome to LookChem.com Sign In|Join Free
  • or
2-Propanone, 1,3-diphenyl-, O-methyloxime is an organic compound with the chemical formula C17H17NO. It is derived from 2-propanone (acetone) and features two phenyl groups attached to the carbon atoms at positions 1 and 3. The O-methyloxime functional group is formed by the reaction of the carbonyl group in 2-propanone with hydroxylamine, followed by the addition of a methyl group to the oxygen atom. 2-Propanone, 1,3-diphenyl-, O-methyloxime is a colorless to pale yellow solid and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is also known for its potential applications in the field of analytical chemistry as a reagent for the detection and determination of metal ions.

2913-02-2

Post Buying Request

2913-02-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

2913-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2913-02-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,1 and 3 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2913-02:
(6*2)+(5*9)+(4*1)+(3*3)+(2*0)+(1*2)=72
72 % 10 = 2
So 2913-02-2 is a valid CAS Registry Number.

2913-02-2SDS

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 1,3-Diphenylacetone O-methyloxime

1.2 Other means of identification

Product number -
Other names Dibenzylketoxim-O-methylether

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:2913-02-2 SDS

2913-02-2Relevant academic research and scientific papers

Carbon Acidity. 79. Acidity of Enolate Equivalent Compounds: Oxime Ethers

Ciula, James C.,Streitwieser, Andrew

, p. 1989 - 1993 (2007/10/02)

A series of benzylic oxime ethers were synthesized (CH3ON=C(CH2Ar)2, Ar = phenyl (1), 4-biphenylyl (2), 1-naphthyl (3), and the equilibrium ion pair acidities in THF were determined.The lithium ion pair acidity of 1 was found to be approximately 5 pK units lower than the corresponding cesium ion pair acidity.The oxime ethers are approximately 10 orders of magnitude less acidic than their corresponding ketones for cesium ion pairs.Thermodynamic parameters for the equilibrium acidities were measured and are consistent for contact ion pair monomers being the important species in solution.An aggregation study also indicated that these cesium oxime ether enolates exist mainly as ion pair monomers.The role of gegenion in the stability of oxime ether anions is discussed.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 2913-02-2