Welcome to LookChem.com Sign In|Join Free
  • or
The term "4,5-epoxy-" refers to a specific type of chemical structure found in certain organic compounds. An epoxy group, which is a three-membered ring consisting of two carbon atoms and one oxygen atom, is denoted as "epoxy." When the epoxy group is located between the 4th and 5th carbon atoms in a molecule, it is described as "4,5-epoxy." This structural feature is significant as it can influence the reactivity, stability, and biological activity of the compound. Compounds with a 4,5-epoxy structure are found in various applications, including pharmaceuticals, where they may serve as intermediates in the synthesis of drugs, and in materials science, where they can be used in the production of polymers and resins. The 4,5-epoxy group can also be a key functional group in natural products, such as certain alkaloids, and plays a role in their chemical properties and potential biological effects.

6790-41-6

Post Buying Request

6790-41-6 Suppliers

Recommended suppliers

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

6790-41-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6790-41-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,9 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6790-41:
(6*6)+(5*7)+(4*9)+(3*0)+(2*4)+(1*1)=116
116 % 10 = 6
So 6790-41-6 is a valid CAS Registry Number.

6790-41-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-(1-Propenyl)oxiran

1.2 Other means of identification

Product number -
Other names (+/-)-trans-propenyl-oxirane

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:6790-41-6 SDS

6790-41-6Downstream Products

6790-41-6Relevant academic research and scientific papers

Deamination Reactions, 41. Reactions of Aliphatic Diazonium Ions and Carbocations with Ethers

Kirmse, Wolfgang,Jansen, Ulrich

, p. 2607 - 2625 (2007/10/02)

Aliphatic diazonium ions and carbocations were generated by deacylation of appropriate nitrosoureas (1, 5, 9) in alcohol-ether mixtures or in 2-alkoxyethanols.Ethers were generally inferior to alcohols in capturing cationic intermediates.Formation of trialkyloxonium ions led to alkyl exchange or ring opening.The observed reactivity orders were n-butyl > isobutyl for the diazonium ions, allyl > sec-butyl > tert-butyl for the carbocations, methoxy > ethoxy and oxirane > oxetane > tetrahydrofuran for the ethers, indicating the predominance of steric effects.Neighboring group participation in 4-methoxy-1-butanediazonium ions (58) and 4,5-epoxy-1-pentanediazonium ions (74) was detectable but inefficient ( 20percent of cyclic oxonium ions).

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 6790-41-6