1516-65-0

• 

• Basic information

  1. Product Name: 2-Butene,1,1,1,2,3,4,4,4-octafluoro-, (2Z)-
  2. Synonyms: 2-Butene,1,1,1,2,3,4,4,4-octafluoro-, (Z)- (8CI); (Z)-Perfluoro-2-butene; cis-Octafluoro-2-butene; cis-Perfluoro-2-butene
  3. CAS NO:1516-65-0
  4. Molecular Formula: C₄F₈
  5. Molecular Weight: 200.03
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 1516-65-0.mol
  9. Article Data: 12

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 8.3°Cat760mmHg
  3. Flash Point: °C
  4. Appearance: N/A
  5. Density: 1.521g/cm³
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: 2-Butene,1,1,1,2,3,4,4,4-octafluoro-, (2Z)-(CAS DataBase Reference)
  10. NIST Chemistry Reference: 2-Butene,1,1,1,2,3,4,4,4-octafluoro-, (2Z)-(1516-65-0)
  11. EPA Substance Registry System: 2-Butene,1,1,1,2,3,4,4,4-octafluoro-, (2Z)-(1516-65-0)

• 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: 1516-65-0(Hazardous Substances Data)

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• Usage
• SDS
• Upstream product
• Downstream Products
• Article

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• 2-Butene,1,1,1,2,3,4,4,4-octafluoro-, (2Z)-

  Cas No: 1516-65-0

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1516-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1516-65-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,1 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1516-65:
(6*1)+(5*5)+(4*1)+(3*6)+(2*6)+(1*5)=70
70 % 10 = 0
So 1516-65-0 is a valid CAS Registry Number.

1516-65-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name	(Z)-1,1,1,2,3,4,4,4-octafluorobut-2-ene

1.2 Other means of identification

Product number	-
Other names	EINECS 216-168-5

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:1516-65-0 SDS

1516-65-0Upstream product

• 375-51-9 1,1,1,2,2,3,4,4,4-nonafluoro-3-iodo-butane 
• 375-26-8 2,3-dibromo-octafluorobutane 
• 357-26-6 octafluoro-1-butene 
• 354-89-2 (pentafluoro ethyl) trifluoro silane 
• 58734-88-6 bis(trifluoromethyl)hexafluoroisopropylphosphine 
• 1463487-28-6 C₆F₁₆Si 
• 303-04-8 2,3-dichloro-1,1,1,4,4,4-hexafluoro-2-butene 
• 1516-64-9 (E)-perfluoro-2-butene 
• 116-14-3 polytetrafluoroethylene 
• 336-23-2 nonafluoropentanoic acid; potassium salt 
• 379-16-8 perfluoro(methylcyclopropane) 

1516-65-0Downstream Products

• 353-50-4 Carbonyl fluoride 
• 354-34-7 trifluoroacetyl fluoride 

1516-65-0Relevant articles and documents

Synthesis of tris- and tetrakis(pentafluoroethyl)silanes

Steinhauer, Simon,Bader, Julia,Stammler, Hans-Georg,Ignat'Ev, Nikolai,Hoge, Berthold

supporting information, p. 5206 - 5209 (2014/05/20)

The synthesis and complete characterization of functional, highly Lewis acidic tris(pentafluoroethyl)silanes as well as tetrakis(perfluoroalkyl)silanes Si(C2F5)4 and Si(C2F 5)3CF3 by direct fluorination is described. The reaction of SiCl4 with LiC2F5 invariably affords (pentafluoroethyl)fluorosilicates. To avoid silicate formation by fluoride transfer from LiC2F5 the Lewis acidity of the silane has to be decreased by electron-donating substituents, such as dialkylamino groups. The easily accessible Si(C2F5) 3NEt2 is a valuable precursor for a series of tris(pentafluoroethyl)silanes. Special eFfects: functional and highly Lewis acidic tris(pentafluoroethyl)silanes as well as the tetrakis(perfluoroalkyl) silanes Si(C2F5)4 and Si(C2F 5)3CF3 are prepared. The two tetrakis species were formed in the direct fluorination of tris-(pentafluoroethyl)ethyl- and methylsilane. Si(C2F5)4 was characterized by X-ray crystallography (see figure).

Fluorine chemistry - Wittig based synthesis of volatile organofluorine compounds

Bhadury, Pinaki S.,Singh, Sapna,Sharma, Mamta,Palit, Meehir,Jaiswal, Devendra K.

, p. 1186 - 1191 (2007/10/03)

A simple and practical method has been developed for the synthesis and characterization of several interesting classes of volatile organofluorine compounds from fluorophosphonium salts via their in situ generated corresponding ylides. The fluorinated phosphonium ylides react with hexafluoroacetone in DMF to generate perfluoroisobutylene, whereas in the presence of bromine or iodine containing electrophiles, tetrafluoroethylene, perfluoro-2-butene, perfluorocyclobutane, and 1H-heptafluoropropane are obtained.

RELATIONSHIPS IN THE IODOFLUORINATION OF FLUOROOLEFINS IN THE IODINE-IODINE PENTAFLUORIDE-METAL FLUORIDE SYSTEM

Morozov, A. V.,Maksimov, B. N.

, p. 1224 - 1229 (2007/10/03)

On the basis of the results from investigation of the reaction of fluoroolefins with the components of the iodine-iodine pentafluoride-metal fluoride iodofluorinating system and kinetic and spectroscopic investigations a mechanism is proposed for the iodofluorination of fluoroolefins as the conjugate addition of iodine and fluorine with initial electrophilic attack on the multiple bond by the I2+ cation.The role of mass exchange during synthesis in a flow-type system is noted.

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