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1-Hexanol, 6-(4-bromophenoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 133080-87-2 Structure
  • Basic information

    1. Product Name: 1-Hexanol, 6-(4-bromophenoxy)-
    2. Synonyms:
    3. CAS NO:133080-87-2
    4. Molecular Formula: C12H17BrO2
    5. Molecular Weight: 273.17
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133080-87-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-Hexanol, 6-(4-bromophenoxy)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Hexanol, 6-(4-bromophenoxy)-(133080-87-2)
    11. EPA Substance Registry System: 1-Hexanol, 6-(4-bromophenoxy)-(133080-87-2)
  • 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: 133080-87-2(Hazardous Substances Data)

133080-87-2 Usage

Physical state

Colorless liquid

Odor

Fruity

Uses

Solvent in various industries, production of perfumes, flavors, and pharmaceuticals, intermediate in the synthesis of other organic compounds, potential applications in organic synthesis and chemical research

Derivative of

1-hexanol

Unique property

Presence of the bromophenoxy group

Check Digit Verification of cas no

The CAS Registry Mumber 133080-87-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,0,8 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 133080-87:
(8*1)+(7*3)+(6*3)+(5*0)+(4*8)+(3*0)+(2*8)+(1*7)=102
102 % 10 = 2
So 133080-87-2 is a valid CAS Registry Number.

133080-87-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(4-bromophenoxy)hexan-1-ol

1.2 Other means of identification

Product number -
Other names -

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:133080-87-2 SDS

133080-87-2Relevant articles and documents

Hydroxy-terminated organic semiconductor-based field-effect transistors for phosphonate vapor detection

Huang, Jia,Miragliotta, Joseph,Becknell, Alan,Katz, Howard E.

, p. 9366 - 9376 (2007)

Organic field-effect transistors (OFETs) with a hydroxy-functionalized semiconductor incorporated into a receptor layer were fabricated and shown to respond strongly to the analyte dimethyl methylphosphonate (DMMP) that simulates phosphonate nerve agents.

Polymer-Supported Chiral-at-Metal Lewis Acid Catalysts

Larionov, Vladimir A.,Cruchter, Thomas,Mietke, Thomas,Meggers, Eric

, p. 1457 - 1460 (2017)

The covalent immobilization of a chiral-at-metal bis-cyclometalated iridium(III) catalyst on a solid support is reported, and its catalytic activity has been investigated. As a catalyst immobilization strategy, a catalyst precursor was tethered to polystyrene macrobeads through an ester or amide linkage and subsequently converted to the immobilized active chiral Lewis acid by treatment with a Br?nsted acid. The amide-linked catalyst displays high robustness and can be recycled multiple times without deterioration of enantioselectivity and only a gradual loss of catalytic activity. Chiral Lewis acid activity was demonstrated as an example for the enantioselective Friedel-Crafts alkylation of indole with an α,β-unsaturated 2-acyl imidazole and for the enantioselective Diels-Alder reactions of an α,β-unsaturated 2-acyl imidazole with 2,3-dihydrofuran or isoprene.

Molecular ordering in bis(phenylenyl)bithiophenes

Stokes, Melissa A.,Kortan, Refik,Amy, Sandrine Rivillon,Katz, Howard E.,Chabal, Yves J.,Kloc, Christian,Siegrist, Theo

, p. 3427 - 3432 (2008/09/21)

The crystal structure of phenylene-bithiophene oligomers (PTTP) has been investigated by powder X-ray diffraction measurements and ab initio Monte Carlo modelling. Two new hydroxyl-terminated PTTP powders, 5,5′-bis-4-(6- hydroxyhexyloxy)-phenyl-2,2′-bithi

Alternating oligo(p-phenylene vinylene)-perylene bisimide copolymers: Synthesis, photophysics, and photovoltaic properties of a new class of donor-acceptor materials

Neuteboom, Edda E.,Meskers, Stefan C. J.,Van Hal, Paul A.,Van Duren, Jeroen K. J.,Meijer,Janssen, Rene A. J.,Dupin, Helene,Pourtois, Geoffrey,Cornil, Jerome,Lazzaroni, Roberto,Bredas, Jean-Luc,Beljonne, David

, p. 8625 - 8638 (2007/10/03)

A Suzuki polycondensation reaction has been used to synthesize two copolymers consisting of alternating oligo(p-phenylene vinylene) (OPV) donor and perylene bisimide (PERY) acceptor chromophores. The copolymers differ by the length of the saturated spacer that connects the OPV and PERY units. Photoinduced singlet energy transfer and photoinduced charge separation in these polychromophores have been studied in solution and in the solid state via photoluminescence and femtosecond pump-probe spectroscopy. In both polymers a photoinduced electron transfer occurs within a few picoseconds after excitation of the OPV or the PERY chromophore. The electron transfer from OPV excited state competes with a singlet energy transfer state to the PERY chromophore. The differences in rate constants for the electron- and energy-transfer processes are discussed on the basis of correlated quantum-chemical calculations and in terms of conformational preferences and folding of the two polymers. In solution, the lifetime of the charge-separated state is longer than in the films where geminate recombination is much faster. However, in the films some charges are able to escape from geminate recombination and diffuse away and can be collected at the electrodes when the polymers are incorporated in a photovoltaic device.

POLYMERIZABLE COMPOSITION SHOWING LIQUID-CRYSTAL PHASE AND OPTICALLY ANISOTROPIC OBJECT MADE WITH THE SAME

-

Page 77, (2008/06/13)

An object of the present invention is to provide a polymerizable liquid crystal composition incorporating a polymerizable liquid crystal compound which displays a low nematic phase temperature, displays excellent compatibility with other polymerizable liquid crystal compounds, and furthermore yields a product following polymerization, of good transparency and high mechanical strength. A polymerizable composition is provided which displays a liquid crystal phase, and moreover incorporates a liquid crystal backbone with two or more ring structures and a compound with a partial structure represented by the general formulaP-S-A-D-E- [wherein P1 represents a polymerizable functional group; S1 represents -(CH2)w-, - O(CH2)w-, -(CH2)wO-, -(CH2)wC(=O)O-, -(CH2)wOC(=O)-, -C(=O)O(CH2)w- or - OC(=O)(CH2)w- (w: 1 to 20); A1 and E1 each represent a hydrocarbon ring or a hetero ring, although E1 is a ring incorporated within the liquid crystal backbone; and D1 represents - C(=O)-O-(CH2)m-O-, -O(CH2)m-O-C(=O)-, -O-C(=O)-(CH2)m-O-, or -O(CH2)m-C(=O)-O- (m: 1 to 15)].

Synthesis and Characterization of Side-Chain Liquid Crystalline Polymethacrylates Containing Fluorinated Diphenyldiacetylene Side-Groups

Lu, Y.-H.,Tsay, K.-T.,Hsu, C.-S.,Chang, H.-L.

, p. 85 - 98 (2007/10/02)

The synthesis of four side-chai liquid crystalline polymethacrylates containing either 4-alkanyloxy-4'-fluorodiphenydiacetylenes or 4-alkanyloxy-3',4'-difluorodiphenyldiacetylenes side groups is presented.The phase behavior of both monomeric and polymeric

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