Welcome to LookChem.com Sign In|Join Free
  • or
Allyl, pentafluoro-, radical is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38683-48-6

Post Buying Request

38683-48-6 Suppliers

Recommended suppliers

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

38683-48-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38683-48-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,6,8 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 38683-48:
(7*3)+(6*8)+(5*6)+(4*8)+(3*3)+(2*4)+(1*8)=156
156 % 10 = 6
So 38683-48-6 is a valid CAS Registry Number.
InChI:InChI=1/C3F5/c4-1(2(5)6)3(7)8

38683-48-6SDS

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 1,1,2,3,3-pentafluoroprop-1-ene

1.2 Other means of identification

Product number -
Other names 1,1,2,3,3-pentafluoro-prop-1->3-enylium

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:38683-48-6 SDS

38683-48-6Downstream Products

38683-48-6Relevant academic research and scientific papers

Infrared multiphoton dissociation of two perfluorobutenes

Longfellow, Cheryl A.,Berrie, Cindy L.,Suits, Arthur G.,Lee, Yuan T.

, p. 7202 - 7208 (2007/10/03)

Photofragment translational spectroscopy was used to examine the infrared multiphoton dissociation of octafluoro-1-butene and octafluoro-2-butene. The predominant unimolecular reaction in octafluoro-1-butene at moderate laser fluences is cleavage of a carbon-carbon single bond to give the products CF3 and C3F5. The two other reactions that take place are CF2 elimination and the formation of equal weight fragments with the chemical composition C2F4; both reactions take place via a diradical intermediate. Dissociation of octafluoro-1-butene to the resonance stabilized perfluoroallyl radical is suggested to account for the favoring of simple bond rupture. These three reaction pathways were also observed in octafluoro-2-butene dissociation, however, the branching fraction is different than from octafluoro-1-butene. In octafluoro-2-butene all three channels occur with roughly equal probability. The reactions involving CF2 loss and C2F4 formation in octafluoro-2-butene are thought to proceed through the same diradical intermediate as in octafluoro-1-butene, necessitating a 1,2-fluorine migration.

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 38683-48-6