Welcome to LookChem.com Sign In|Join Free
  • or
(1R,4R,6R)-4-tert-butyl-1-phenyl-7-oxabicyclo[4.1.0]heptane is a complex organic compound characterized by its unique molecular structure. It features a seven-membered ring with an oxygen atom, forming a bridge between two carbon atoms, which classifies it as a bicyclic compound. The molecule has three chiral centers, indicated by the R-configuration at positions 1, 4, and 6, which means all three centers have the same spatial arrangement. The presence of a tert-butyl group at position 4 and a phenyl group at position 1 adds to its structural complexity. (1R,4R,6R)-4-tert-butyl-1-phenyl-7-oxabicyclo[4.1.0]heptane is of interest in organic chemistry due to its potential applications in the synthesis of pharmaceuticals and other specialty chemicals, where its stereochemistry plays a crucial role in determining its reactivity and biological activity.

4341-22-4

Post Buying Request

4341-22-4 Suppliers

Recommended suppliers

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

4341-22-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4341-22-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,4 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4341-22:
(6*4)+(5*3)+(4*4)+(3*1)+(2*2)+(1*2)=64
64 % 10 = 4
So 4341-22-4 is a valid CAS Registry Number.

4341-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,3R,6R)-3-tert-butyl-6-phenyl-7-oxabicyclo[4.1.0]heptane

1.2 Other means of identification

Product number -
Other names 7-Oxabicyclo(4.1.0)heptane,4-(1,1-dimethylethyl)-1-phenyl-,(1alpha,4beta,6alpha)

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:4341-22-4 SDS

4341-22-4Relevant academic research and scientific papers

A FACILE ROUTE TO IODOHYDRINS AND EPOXIDES BY OXIDATION OF OLEFIN-IODINE COMPLEXES WITH PYRIDINIUM DICHROMATE

Antonioletti, Roberto,D'Auria, Maurizio,Mico, Antonella De,Piancatelli, Giovanni,Scettri, Arrigo

, p. 1765 - 1768 (2007/10/02)

Trisubstituted olefins, activated with I2, are changed into iodohydrins and epoxides by pyridinium dichromate.The conversion shows to proceed in regiospecific and stereospecific manner.Moreover some naturally occurring polyenes, submitted to similar treatment, afford selectively only terminal iodohydrins.These latter are converted into the corresponding epoxides through a new and convenient alumina supported reaction.

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 4341-22-4