Welcome to LookChem.com Sign In|Join Free
  • or
7-Oxabicyclo[4.2.0]octane is a cyclic organic compound characterized by a seven-membered ring structure, which includes one oxygen atom and six carbon atoms. The presence of the oxygen atom in the ring system imparts unique chemical properties to the molecule, distinguishing it from other hydrocarbons. 7-oxabicyclo[4.2.0]octane is often used as a building block in the synthesis of various pharmaceuticals and other organic compounds due to its rigid and strained ring structure, which can influence the reactivity and selectivity of chemical reactions. Its unique properties make it a valuable intermediate in organic synthesis, particularly in the preparation of complex molecules with potential applications in medicine and other industries.

278-38-6

Post Buying Request

278-38-6 Suppliers

Recommended suppliers

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

278-38-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 278-38-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,7 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 278-38:
(5*2)+(4*7)+(3*8)+(2*3)+(1*8)=76
76 % 10 = 6
So 278-38-6 is a valid CAS Registry Number.

278-38-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Oxabicyclo[4.2.0]octane

1.2 Other means of identification

Product number -
Other names (+-)-cis-hexahydro-benzoxete

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:278-38-6 SDS

278-38-6Downstream Products

278-38-6Relevant academic research and scientific papers

Stereochemistry of the Conversion of 1,3-Chloroalcohols in Alkaline Medium The Chemistry of 1,3-Bifunctional Systems. XXII

Bartok, Mihaly,Felfoeldi, Karoly,Bozoki-Bartok, Gizella

, p. 2173 - 2178 (2007/10/02)

The transformation of isomeric 1,3-Chloroalcohols 1-4, with cyclohexane skeleton, were studied in aqueous solution containing barium hydroxide.As regards the compounds with cis-configuration, 1 gives the oxetane 5 by intramolecular nucleophilic substitution, while 3 gives the unsatured alcohols 7 and 8 by elimination.In the case of the trans-isomers 2 and 4, fragmentation reactions occur in competition with elimination.The main reaction kinetic parameters of the transformations of the four compounds were determined.

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 278-38-6