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1-BROMO-4-(1H,1H,2H,2H-PERFLUOROPENTYL)BENZENE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

195324-88-0

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195324-88-0 Usage

Explanation

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

Explanation

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

Explanation

A perfluoropentyl group is a five-carbon chain with all hydrogen atoms replaced by fluorine atoms. In 1-BROMO-4-(1H,1H,2H,2H-PERFLUOROPENTYL)BENZENE, the perfluoropentyl group is attached to the benzene ring.
5. Benzene ring

Explanation

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

Explanation

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

Explanation

1-BROMO-4-(1H,1H,2H,2H-PERFLUOROPENTYL)BENZENE 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

Explanation

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

Explanation

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 1-BROMO-4-(1H,1H,2H,2H-PERFLUOROPENTYL)BENZENE.

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

Fluorous synthesis of mono-dispersed poly(ethylene glycols)

Li, Yu,Guo, Qi,Li, Xuefei,Zhang, Hua,Yu, Fanghua,Yu, Weijiang,Xia, Guiquan,Fu, Mingyang,Yang, Zhigang,Jiang, Zhong-Xing

supporting information, p. 2110 - 2113 (2014/04/03)

Mono-dispersed poly(ethylene glycols) (PEGs) are of great value in the development of biopharmaceuticals. However, tedious synthesis limits the availability of mono-dispersed PEGs. To address this issue, a fluorous synthesis of mono-dispersed PEGs, discretely PEGylated surfactants and 19F magnetic resonance imaging (MRI) agents has been developed. During the synthesis, both fluorous and normal phase silica gel-based solid-phase extractions were successfully employed to simplify the purifications. This synthesis provided an easy access to valuable mono-dispersed PEGs and related molecules for biomedical application on multi-gram scales.

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.

Thiol additions to acrylates by fluorous mixture synthesis: Relative control of elution order in demixing by the fluorous tag and the thiol substituent

Curran, Dennis P.,Oderaotoshi, Yoji

, p. 5243 - 5253 (2007/10/03)

All possible combinations of a series of three fluorous benzyl tags and three acrylates have been made. The resulting acrylate esters were combined in groups of three (one of each tag) and the resulting mixtures were reacted with a mixture of four thiols under standard conditions to effect conjugate addition. Analysis of the resulting libraries by fluorous hplc showed a primary separation based on the tag and revealed reliable secondary separations based on the thiol and the acrylate. The primary and secondary separations were used together in a preparative 'mixture of mixtures' experiment in which one of the tagged acrylate mixtures was reacted with a mixture of three thiols. The resulting nine component mixture was demixed by fluorous and reverse phase hplc and then detagged to give all nine final products in pure form.

Perfluoroalkyl-substituted arylphosphanes as ligands for homogeneous catalysis in supercritical carbon dioxide

Kainz,Koch,Baumann,Leitner

, p. 1628 - 1630 (2007/10/03)

The solubility of complexes is one decisive factor for their use as homogeneous catalysts in supercritical carbon dioxide (scCO2). Complexes with perfluoroalkyl-substituted arylphosphane ligands (shown schematically on the right), which can be

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