Welcome to LookChem.com Sign In|Join Free

CAS

  • or

195324-88-0

Post Buying Request

195324-88-0 Suppliers

Recommended suppliersmore

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

195324-88-0 Usage

Explanation

Different sources of media describe the Explanation of 195324-88-0 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 13 carbon (C) atoms, 5 hydrogen (H) atoms, 1 bromine (Br) atom, and 17 fluorine (F) atoms.
2. Perfluorinated aromatic compound
3. Bromine atom
2. The presence of a bromine atom (Br) in the compound indicates that it has a bromine substituent attached to the benzene ring.
4. Perfluoropentyl group
3. A perfluoropentyl group is a five-carbon chain with all hydrogen atoms replaced by fluorine atoms. In this compound, the perfluoropentyl group is attached to the benzene ring.
5. Benzene ring
4. The benzene ring is a six-carbon ring with alternating single and double bonds between the carbon atoms. It is a common structural feature in many organic compounds.
6. Synthesis of organic compounds
5. 1-Bromo-4-(1H,1H,2H,2H-perfluoropentyl)benzene is used as a starting material or intermediate in the synthesis of various organic compounds and materials.
7. Reagent in chemical research and manufacturing
6. This compound is utilized as a reagent, which is a substance or compound used to initiate or facilitate a chemical reaction in research and manufacturing processes.
8. Flammability
7. The compound is flammable, which means it can easily catch fire and burn. This property requires careful handling and storage to prevent accidents.
9. Health and environmental hazards
8. Due to its chemical nature, 1-Bromo-4-(1H,1H,2H,2H-perfluoropentyl)benzene may pose risks to human health and the environment if not properly managed. It is essential to follow safety guidelines and regulations when handling this compound.

Check Digit Verification of cas no

The CAS Registry Mumber 195324-88-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,3,2 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 195324-88:
(8*1)+(7*9)+(6*5)+(5*3)+(4*2)+(3*4)+(2*8)+(1*8)=160
160 % 10 = 0
So 195324-88-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H8BrF17/c17-8-3-1-7(2-4-8)5-6-9(18,19)10(20,21)11(22,23)12(24,25)13(26,27)14(28,29)15(30,31)16(32,33)34/h1-4H,5-6H2

195324-88-0SDS

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 1-bromo-4-(1,1,2,2,3,3,4,4,5,5,6,6,7,7,10,10,10-heptadecafluorodecyl)benzene

1.2 Other means of identification

Product number -
Other names bromo-4-(3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl)benzene

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:195324-88-0 SDS

195324-88-0Downstream Products

195324-88-0Relevant articles and documents

A novel macroreticular-type fluorous polystyrene resin and its application to the synthesis of a 3-amino-β-carboline derivative with N-methyl-N-nitrosourea conjugation via fluorous solid-phase reaction: A comparative study of fluorous solid-, solid-, and

Suzuki, Keiko,Kumagai, Munenori,Utsunomiya, Masamichi,Sakai, Norio,Konakahara, Takeo

, p. 4999 - 5012 (2015)

A novel fluorous polystyrene (FPS) MR-resin was applied to a fluorous solid-phase (FSP) reaction. The MR-FPS resin actually was developed previously and possessed excellent chemical resistance to acids and alkalis, and a fluorous-tagged compound was homog

Efficient access to perfluoroalkylated aryl compounds by Heck reaction

Darses, Sylvain,Pucheault, Mathieu,Genet, Jean-Pierre

, p. 1121 - 1128 (2007/10/03)

Efficient introduction of perfluorinated tails onto aromatic rings has been achieved by Heck reaction between perfluoroalkenes and arenediazonium salts, catalysed by palladium acetate. Subsequent transition metal catalysed hydrogenation of the double bond afforded a large variety of aromatic compounds bearing an affinity for fluorous solvents. Formation of perfluoroalkylated phosphane ligands and their use in palladium-catalysed coupling between potassium trifluoro(vinyl)borates and diazonium salts is also described, allowing an easy separation and recycling of the catalytic system.

Repetitive Application of Perfluoro-Tagged Pd Complexes for Stille Coupling in a Fluorous Biphasic System

Schneider, Siegfried,Bannwarth, Willi

, p. 4142 - 4145 (2007/10/03)

-

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 195324-88-0