Welcome to LookChem.com Sign In|Join Free
  • or
Oxetane, 2,2-diphenyl-, also known as 2,2-diphenyloxetane, is a cyclic ether compound with the molecular formula C14H14O. It features a four-membered oxetane ring, which consists of three carbon atoms and one oxygen atom, with two phenyl groups attached to the carbon atoms at the 2-position. This organic compound is characterized by its aromatic nature due to the presence of the phenyl groups, which contribute to its stability and chemical properties. 2,2-diphenyloxetane is an important intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals, owing to its unique structure and reactivity. It is typically synthesized through various methods, such as the reaction of phenylmagnesium bromide with 1,2-epoxy-1,2-diphenylethane or the intramolecular cyclization of 2-phenylallyl alcohol. The compound is also known for its potential applications in materials science, particularly in the development of new polymers and resins.

884-73-1

Post Buying Request

884-73-1 Suppliers

Recommended suppliers

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

884-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 884-73-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,8 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 884-73:
(5*8)+(4*8)+(3*4)+(2*7)+(1*3)=101
101 % 10 = 1
So 884-73-1 is a valid CAS Registry Number.

884-73-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-diphenyloxetane

1.2 Other means of identification

Product number -
Other names 2,2-Diphenyl-oxetan

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:884-73-1 SDS

884-73-1Relevant academic research and scientific papers

Reaction of sulfonimidamide Anions with Electrophiles

Okuma, Kentaro,Koike, Tetsufumi,Ohta, Hiroshi

, p. 4190 - 4193 (2007/10/02)

The reaction of alkylsulfonimidamides with bases gave corresponding carboanions, which were allowed to react with carbonyl compounds to give (2-hydroxyalkyl)sulfonimidamides in good yields.When benzoic anhydride or chlorotrimethylsilane was treated with these anions, corresponding phenacylsulfonimidamides or (trimethylsilyl)methylsulfonimidamides were obtained.On the other hand, the reaction of methyl N-p-tosylsulfonimidmorpholide anion with carbonyl compounds afforded epoxides or oxetanes in good yields.

NOVEL REACTIONS OF AMINOSULFOXONIUM YLIDE WITH EPOXIDES

Okuma, Kentaro,Nishimura, Kenshin,Ohta, Hiroshi

, p. 93 - 96 (2007/10/02)

Reactions of (dimethylamino)phenyloxosulfonium methylide with epoxides were carried out.When aromatic epoxides were used as substrates, cyclopropyl sulfones and oxetanes were obtained.When aliphatic epoxides were used, the products were only the cycloprop

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 884-73-1