Welcome to LookChem.com Sign In|Join Free

CAS

  • or

4806-61-5

1-Ethylcyclobutane, with the molecular formula C8H16, is a cyclic organic compound characterized by a four-carbon ring structure with an ethyl group attached to one of the carbon atoms. It falls under the category of alkylcycloalkanes and is recognized for its colorless liquid state at room temperature and its slight odor. Due to its flammable nature and potential harmful effects if ingested or inhaled, it requires careful handling and storage.

4806-61-5 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 4806-61-5 Structure

  • Basic information

    1. Product Name: 1-ETHYLCYCLOBUTANE
    2. Synonyms: Ethylcyclobutane;ethyl-cyclobutane;1-ETHYLCYCLOBUTANE
    3. CAS NO:4806-61-5
    4. Molecular Formula: C6H12
    5. Molecular Weight: 84.16
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 4806-61-5.mol

  • Chemical Properties

    1. Melting Point: -142.75°C
    2. Boiling Point: 70.65°C
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 0.7232
    6. Vapor Pressure: 139mmHg at 25°C
    7. Refractive Index: 1.3994
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-ETHYLCYCLOBUTANE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-ETHYLCYCLOBUTANE(4806-61-5)
    12. EPA Substance Registry System: 1-ETHYLCYCLOBUTANE(4806-61-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 4806-61-5(Hazardous Substances Data)

4806-61-5 Usage

Uses

Used in Chemical Synthesis Industry:
1-Ethylcyclobutane serves as a starting material or intermediate in the synthesis of other organic compounds, playing a crucial role in the creation of various chemical products. Its unique structure and reactivity make it a valuable component in the development of new molecules and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 4806-61-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,0 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4806-61:
(6*4)+(5*8)+(4*0)+(3*6)+(2*6)+(1*1)=95
95 % 10 = 5
So 4806-61-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H12/c1-2-6-4-3-5-6/h6H,2-5H2,1H3

4806-61-5SDS

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 ethylcyclobutane

1.2 Other means of identification

Product number -
Other names Ethylcyclobutan

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:4806-61-5 SDS

4806-61-5Relevant articles and documents

The Kinetics and Mechanism of Ring Opening of Radicals containing the Cyclobutylcarbinyl System

Beckwith, Athelstan L. J.,Moad, Graeme

, p. 1083 - 1092 (2007/10/02)

The kinetic parameters of β-fission of radicals containing the cyclobutylcarbinyl system have been determined by analysis of the mixtures obtained when suitable chloro-compounds are treated with tributylstannane.Under these conditions ring opening is irreversible and in the rigid bicyclic system (4) is under stereoelectronic control.For ring opening of cyclobutylcarbinyl radical (8) kf = 4.3 x 103 s-1 at 60 deg C, and the best values of the activation parameters appear to be ΔH(excit.) = 12.2 kcal mol-1 and ΔS(excit.) = -7.4 cal mol-1 K-1.Monocyclic systems undergo preferential fission of the more substituted βγ-bond.Methyl substituents at the α-, β-, or δ-positions have little effect but γ-substitution strongly enhances the rate of ring opening.The transition state is reactant-like and has a similar disposition of centres to that (1) for homolytic addition.

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

What can I do for you?
Get Best Price

Get Best Price for 4806-61-5