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N,N-DIHEXYL-4-IODOANILINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 90134-09-1 Structure
  • Basic information

    1. Product Name: N,N-DIHEXYL-4-IODOANILINE
    2. Synonyms: N,N-DIHEXYL-4-IODOANILINE;N,N-DIHEXYL-4-IODOBENZENEAMINE
    3. CAS NO:90134-09-1
    4. Molecular Formula: C18H30IN
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 90134-09-1.mol
  • 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: N,N-DIHEXYL-4-IODOANILINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: N,N-DIHEXYL-4-IODOANILINE(90134-09-1)
    11. EPA Substance Registry System: N,N-DIHEXYL-4-IODOANILINE(90134-09-1)
  • 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: 90134-09-1(Hazardous Substances Data)

90134-09-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90134-09-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,3 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90134-09:
(7*9)+(6*0)+(5*1)+(4*3)+(3*4)+(2*0)+(1*9)=101
101 % 10 = 1
So 90134-09-1 is a valid CAS Registry Number.

90134-09-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dihexyl-4-iodoaniline

1.2 Other means of identification

Product number -
Other names p-iodo-N,N-di-n-hexylaniline

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:90134-09-1 SDS

90134-09-1Relevant articles and documents

Substituent engineering of electrooptic chromophores to suppress their aggregation

Kashiwabara, Kazuki,Inada, Shunsuke,Noguchi, Takamasa,Sato, Yukichi,Kikuchi, Kohei,Imai, Masato,Yamakado, Ryohei,Okada, Shuji

, p. 70 - 77 (2019)

Chromophores composed of 4-cyano-5-dicyanomethylene-2-oxo-3-pyrroline (CDCOP) and a donor have been synthsized for electrooptic applications. Three substituents of [5-(4-aminophenyl)-2-thienyl]-substituted CDCOP 1 and (4-aminophenyl)-substituted CDCOP 2 w

Self-Diagnostic Polymers—Inline Detection of Thermal Degradation of Unsaturated Poly(ester imide)s

Funtan, Alexander,Michael, Philipp,Rost, Simon,Omeis, Jürgen,Lienert, Klaus,Binder, Wolfgang H.

, (2021/04/05)

Monitoring polymer degradation is an important quest, particularly relevant for industry. Although many indirect methodologies for assessing polymer degradation exist, only few are applicable for an inline-monitoring via optic detection-systems. An inline

Synthesis, physical properties, and chemistry of donor-acceptor-substituted pentacenes

Lehnherr, Dan,Adam, Matthias,Murray, Adrian H.,McDonald, Robert,Hampel, Frank,Tykwinski, Rik R.

, p. 303 - 314 (2017/03/09)

Pentacenes bearing electron-donating and (or) -withdrawing groups, namely methoxy-, dialkylamino-, and nitroaryl moieties, are synthesized to afford polarized pentacenes. The optical, electrochemical, and chemical properties of these derivatives are explo

Two-photon absorption properties of proquinoidal D-A-D and A-D-A quadrupolar chromophores

Susumu, Kimihiro,Fisher, Jonathan A.N.,Zheng, Jieru,Beratan, David N.,Yodh, Arjun G.,Therien, Michael J.

scheme or table, p. 5525 - 5539 (2011/08/06)

We report the synthesis, one- and two-photon absorption spectroscopy, fluorescence, and electrochemical properties of a series of quadrupolar molecules that feature proquinoidal p-aromatic acceptors. These quadrupolar molecules possess either donoracceptor donor (D-A-D) or acceptordonoracceptor (A-D-A) electronic motifs, and feature 4-N,N-dihexylaminophenyl, 4-dodecyloxyphenyl, 4-(N,N-dihexylamino)benzo[c][1,2,5]thiadiazolyl or 2,5-dioctyloxyphenyl electron donor moieties and benzo[c][1,2,5]thiadiazole (BTD) or 6,7-bis(30,70-dimethyloctyl)[1,2,5]thiadiazolo[3,4-g]quinoxaline (TDQ) electron acceptor units. These conjugated structures are highly emissive in nonpolar solvents and exhibit large spectral red-shifts of their respective lowest energy absorption bands relative to analogous reference compounds that incorporate phenylene components in place of BTD and TDQ moieties. BTD-based D-A-D and A-D-A chromophores exhibit increasing fluorescence emission redshifts, and a concomitant decrease of the fluorescence quantum yield (Ff) with increasing solvent polarity; these data indicate that electronic excitation augments benzothiadiazole electron density via an internal charge transfer mechanism. The BTD- and TDQcontaining structures exhibit blue-shifted two-photon absorption (TPA) spectra relative to their corresponding one-photon absorption (OPA) spectra, and display high TPA cross sections (>100 GM) within these spectral windows. D-A-D and A-D-A structures that feature more extensive conjugation within this series of compounds exhibit larger TPA cross sections consistent with computational simulation. Factors governing TPA properties of these quadrupolar chromophores are discussed within the context of a three-state model.

FLUORESCENT SOLVATOCHROMIC PIGMENT

-

Page/Page column 8, (2012/01/03)

The present invention presents a novel fluorescent solvatochromic dye that (1) has an ionic terminal that makes it easier to use n a hydrophilic surface or in polar solvents, (2) can be efficiently excited by commonly used Argon lasers (488 nm), (3) shift

A cheap and efficient method for selective para-iodination of aniline derivatives

Monnereau, Cyrille,Blart, Errol,Odobel, Fabrice

, p. 5421 - 5423 (2007/10/03)

A new and cheap protocol for controlled iodination in the para-position of various aniline derivatives is presented. It operates under mild conditions by reacting the aniline derivatives with molecular iodine in a mixture of pyridine/dioxane (1/1 vol) at 0°C.

Donor-substituted perethynylated dehydroannulenes and radiaannulenes: Acetylenic carbon sheets featuring intense intramolecular charge transfer

Mitzel, Frieder,Boudon, Corinne,Gisselbrecht, Jean-Paul,Seiler, Paul,Gross, Maurice,Diederich, Francois

, p. 1130 - 1157 (2007/10/03)

In this article, we report the preparation of unprecedented φ-conjugated macrocycles (Fig. 1) by acetylenic scaffolding using modular tetraethynylethene (TEE, 3,4-diethynylhex-3-ene-1,5-diyne) building blocks. A novel photochemical access to (Z)-bisdeprot

Hexasubstituted Donor-Acceptor Benzenes as Nonlinear Optically Active Molecules with Multiple Charge-Transfer Transitions

Traber, Boris,Wolff, J. Jens,Rominger, Frank,Oeser, Thomas,Gleiter, Rolf,Goebel, Mark,Wortmann, Ruediger

, p. 1227 - 1238 (2007/10/03)

The synthesis of three novel nonlinear optical (NLO) chromophores with threefold symmetry, namely 1,3,5-tris(4-N,N-diethylaminophenyl)-2,4,6-tris(4-nitrophenyl)benzene (3), 1,3,5-tris(L-N,N-dihexylaminophenylbutadiynyl)-2,4,6-tris(4-nitrophenyl)benzene (1

Metal-catalyzed cross-coupling reactions for the synthesis of functionalized 1,4,5,8-tetraazafulvalenes

Kaepplinger, Christian,Beckert, Rainer

, p. 1843 - 1850 (2007/10/03)

Tetraazafulvalenes can be cross-coupled (palladium-catalyzed) with alkenes or acetylenes. Although Suzuki conditions fail, the Heck and the Sonogashira methods are useful tools for functionalizing tetraazafulvalenes. Starting from the tetraiodoaryl deriva

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