Welcome to LookChem.com Sign In|Join Free
  • or
β-Decalone oxime, also known as 2-oxime-1-decalone, is an organic compound with the chemical formula C10H19NO. It is a derivative of decalone, a cyclic ketone, and is formed by the addition of hydroxylamine to the carbonyl group of decalone, resulting in the formation of an oxime group. β-decalone oxime is characterized by its unique structure, which includes a ten-carbon cyclic ketone with an oxime functional group attached to the second carbon. β-Decalone oxime is used in various applications, such as in the synthesis of pharmaceuticals and other organic compounds, due to its reactivity and the ability to form different types of chemical bonds. It is an important intermediate in organic chemistry, particularly in the preparation of complex molecules that require the presence of a cyclic structure with a reactive oxime group.

91716-73-3

Post Buying Request

91716-73-3 Suppliers

Recommended suppliers

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

91716-73-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91716-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,7,1 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91716-73:
(7*9)+(6*1)+(5*7)+(4*1)+(3*6)+(2*7)+(1*3)=143
143 % 10 = 3
So 91716-73-3 is a valid CAS Registry Number.

91716-73-3Relevant academic research and scientific papers

Reactivite nucleophile des cyclanones: influence de la stereochimie cis/trans en serie bicyclique

Agami, C.,Rizk, T.,Durand, R.,Geneste, P.

, p. 2355 - 2357 (1982)

The relative reactivities of a number of cis/trans pairs of bicyclic ketones in the 1- and 2-decalone series (2-decalone; 10-methyl-2-decalone; 9-methyl-1-decalone; and 3,10-dimethyl-2-decalone) have been studied for the nucleophilic addition of hydroxylamine in acidic medium.The results obtained as well as the rate constants for neutral or acid catalysed addition always reveal a slight preference for the trans-isomer (x 2.4).This result agrees with the proposal that preferential equatorial attack of a nucleophile is caused by conformational factors related to a steroid non-steroid conformation equilibrium in the cis-isomers.

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 91716-73-3