Welcome to LookChem.com Sign In|Join Free
  • or
7-ethoxybicyclo[4.2.0]octa-1,3,5-triene is a chemical compound with the molecular formula C10H12O. It is a colorless liquid with a strong, pungent odor. 7-ethoxybicyclo[4.2.0]octa-1,3,5-triene is characterized by its unique bicyclic structure, featuring a seven-membered ring with an ethoxy group attached to the seventh carbon atom. It is an organic compound that falls under the category of polycyclic aromatic hydrocarbons, specifically a derivative of bicyclo[4.2.0]octa-1,3,5-triene. 7-ethoxybicyclo[4.2.0]octa-1,3,5-triene is primarily used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactive nature, it is essential to handle 7-ethoxybicyclo[4.2.0]octa-1,3,5-triene with care, following proper safety protocols to minimize potential health and environmental risks.

3718-75-0

Post Buying Request

3718-75-0 Suppliers

Recommended suppliers

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

3718-75-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3718-75-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,1 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3718-75:
(6*3)+(5*7)+(4*1)+(3*8)+(2*7)+(1*5)=100
100 % 10 = 0
So 3718-75-0 is a valid CAS Registry Number.

3718-75-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-ethoxybicyclo[4.2.0]octa-1,3,5-triene

1.2 Other means of identification

Product number -
Other names 1-ethoxybenzocyclobutene

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:3718-75-0 SDS

3718-75-0Upstream product

3718-75-0Downstream Products

3718-75-0Relevant academic research and scientific papers

Intramolecular Reactivity of Arylcarbenes: 2-(Alkoxymethyl)phenylcarbenes

Kirmse, Wolfgang,Schnitzler, Dirk

, p. 1699 - 1702 (2007/10/02)

Both singlet and triplet states contribute to the intramolecular C-H insertion reactions of 2-(alkoxymethyl)phenylcarbenes, leading to dihydro-1H-2-benzopyrans.Competitively, oxygen ylides are generated which eventually give rise to benzocyclobutenes and dihydroisobenzofurans.The radical pair mechanism of the Stevens rearrangement is confirmed by variation of the alkyl groups and by means of chiral substrates.

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 3718-75-0