139613-90-4

• 

• Basic information

  1. Product Name: 4-(PERFLUOROHEXYL)ANILINE
  2. Synonyms: 4-(PERFLUOROHEXYL)ANILINE
  3. CAS NO:139613-90-4
  4. Molecular Formula: C₁₂H₆F₁₃N
  5. Molecular Weight: 411.16
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 139613-90-4.mol
  9. Article Data: 10

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: 4-(PERFLUOROHEXYL)ANILINE(CAS DataBase Reference)
  10. NIST Chemistry Reference: 4-(PERFLUOROHEXYL)ANILINE(139613-90-4)
  11. EPA Substance Registry System: 4-(PERFLUOROHEXYL)ANILINE(139613-90-4)

• 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: 139613-90-4(Hazardous Substances Data)

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• SDS
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• Downstream Products
• Article

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• 4-(PERFLUOROHEXYL)ANILINECAS

  Cas No: 139613-90-4

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• Hangzhou Fandachem Co.,Ltd
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• 4-(Perfluorohexyl)aniline

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139613-90-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139613-90-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,6,1 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 139613-90:
(8*1)+(7*3)+(6*9)+(5*6)+(4*1)+(3*3)+(2*9)+(1*0)=144
144 % 10 = 4
So 139613-90-4 is a valid CAS Registry Number.

139613-90-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name	4-(1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexyl)aniline

1.2 Other means of identification

Product number	-
Other names	4-perfluorohexylbenzenamine

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:139613-90-4 SDS

139613-90-4Upstream product

• 355-43-1 n-perfluorohexyl iodide 
• 12775-96-1 copper 
• 540-37-4 p-aminoiodobenzene 
• 335-56-8 1-bromo-1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane 
• 62-53-3 aniline 
• 106-40-1 4-bromo-aniline 

139613-90-4Downstream Products

• 609816-25-3 N-(4-(1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexyl)phenyl)maleimide 
• 1384111-90-3 C₁₆H₈F₁₃NO₃ 
• 326806-93-3 N-[4-(perfluorohexyl)phenyl]-2,4-dinitrobenzenamine 
• 149068-56-4 4-(tridecafluoro-n-hexyl)bromobenzene 
• 193197-68-1 tris(4-tridecafluoro-n-hexylphenyl)phosphine 
• 150956-62-0 4-(4-tridecafluorohexyl-phenylazo)-phenylamine 

139613-90-4Relevant articles and documents

Palladium-catalyzed cross-coupling of organozinc bromides with aryl iodides in perfluorinated solvents

Betzemeier, Bodo,Knochel, Paul

, p. 2623 - 2624 (1997)

-

Towards a practical perfluoroalkylation of (hetero)arenes with perfluoroalkyl bromides using cobalt nanocatalysts

Bartling, Stephan,Beller, Matthias,Ellinger, Stefan,Kreyenschulte, Carsten Robert,Lund, Henrik,Neumann, Helfried,Taeschler, Christoph,Weniger, Florian,Zhang, Shaoke

, p. 1731 - 1738 (2020/04/09)

A convenient methodology for perfluoroalkylation including trifluoromethylation of (hetero)arenes with perfluoroalkyl bromides was developed. Key for the success is the use of a specific cobalt-based nanocatalyst, which can be recycled at least up to 4 times. The scope of this first cobalt-catalyzed perfluoroalkylation is presented and detailed catalyst characterization (e.g. analytical STEM, XPS, and XRD) has been carried out.

Synthesis and X-ray analysis of a perfluoroalkyl-substituted azobenzene dye

He, Liang,Freeman, Harold S.,Nakpathom, Monthon,Boyle, Paul D.

, p. 245 - 250 (2015/08/26)

A search for colorants capable of reducing the surface energy of synthetic fibers as well as adding color led to the synthesis and characterization of the repellency behavior of dyes such as 4-N,N-diethylamino-4′-tridecafluorohexylazobenzene. Unexpectedly

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