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39905-57-2

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39905-57-2 Usage

Uses

4-(Hexyloxy)aniline was used in the synthesis of 4-hydroxy-4′-hexyloxyazobenzene.

Check Digit Verification of cas no

The CAS Registry Mumber 39905-57-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,9,0 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 39905-57:
(7*3)+(6*9)+(5*9)+(4*0)+(3*5)+(2*5)+(1*7)=152
152 % 10 = 2
So 39905-57-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H19NO/c1-2-3-4-5-10-14-12-8-6-11(13)7-9-12/h6-9H,2-5,10,13H2,1H3

39905-57-2 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H55868)  4-n-Hexyloxyaniline, 99%   

  • 39905-57-2

  • 1g

  • 226.0CNY

  • Detail
  • Alfa Aesar

  • (H55868)  4-n-Hexyloxyaniline, 99%   

  • 39905-57-2

  • 5g

  • 792.0CNY

  • Detail
  • Alfa Aesar

  • (H55868)  4-n-Hexyloxyaniline, 99%   

  • 39905-57-2

  • 25g

  • 2809.0CNY

  • Detail

39905-57-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(Hexyloxy)aniline

1.2 Other means of identification

Product number -
Other names 4-Hexyloxyaniline

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:39905-57-2 SDS

39905-57-2Relevant articles and documents

PHOTORESPONSIVE COMPOUND, AND ADHESIVE, TONER AND IMAGE FORMATION METHOD USING THE SAME

-

, (2021/05/07)

PROBLEM TO BE SOLVED: To provide a compound that is fluidized by light irradiation and is un-fluidized reversibly, and shows no excessive coloration. SOLUTION: The present invention relates to a compound of chemical formula 1a or 1b: R1 and r1 each denote a hydrogen atom, a halogen atom or the like; R2-R7 and r2-r7 each denote a group represented by chemical formula 2, a hydrogen atom, a halogen atom or the like, where at least one of R2-R7 and r2-r7 is a group represented by chemical formula 2; in chemical formula 2, X1 and X2 each denote N or CH, and X1≠X2; A1-A5 each denote a hydrogen atom, a halogen atom or the like, where at least one of A1-A5 is an alkyl group, an alkoxy group, an acyl group, an alkoxycarbonyl group, or an acyloxy group. SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

Thermotropic Liquid-Crystalline and Light-Emitting Properties of Bis(4-aalkoxyphenyl) Viologen Bis(triflimide) Salts

Agra-Kooijman, De?a M.,Al-Karawi, Muhammed Kareem M.,Bhowmik, Pradip K.,Chang, Anthony,Chen, Si L.,Cortez, Raymond G.,Dizon, Erenz J.,Fisch, Michael R.,Gutierrez, Bryan,Han, Haesook,Ho, Andy,Killarney, Shane T.,Kim, Jongin,Kumar, Satyendra,Mandal, Hari D.,Mendez, Klarissa,Principe, Ronald Carlo G.,Sharpnack, Lewis

, (2020/05/29)

A series of bis(4-alkoxyphenyl) viologen bis(triflimide) salts with alkoxy chains of different lengths were synthesized by the metathesis reaction of respective bis(4-alkoxyphenyl) viologen dichloride salts, which were in turn prepared from the reaction of Zincke salt with the corresponding 4-n-alkoxyanilines, with lithium triflimide in methanol. Their chemical structures were characterized by 1H and 13C nuclear magnetic resonance spectra and elemental analysis. Their thermotropic liquid-crystalline (LC) properties were examined by differential scanning calorimetry, polarizing optical microscopy, and variable temperature X-ray diffraction. Salts with short length alkoxy chains had crystal-to-liquid transitions. Salts of intermediate length alkoxy chains showed both crystal-to-smectic A (SmA) transitions, Tms, and SmA-to-isotropic transitions, Tis. Those with longer length of alkoxy chains had relatively low Tms at which they formed the SmA phases that persisted up to the decomposition at high temperatures. As expected, all of them had excellent thermal stabilities in the temperature range of 330-370 ?C. Their light-emitting properties in methanol were also included.

Synthesis, liquid crystalline properties and photo switching properties of coumarin-azo bearing aliphatic chains: Application in optical storage devices

Madiahlagan, Eswaran,B N, Sunil,Ngaini, Zainab,Hegde, Gurumurthy

, (2019/07/31)

A series of novel azo-coumarin derivatives with different aliphatic chain length (3a-e) have been synthesized and characterized for liquid crystal properties and their photoswitching behavior. The incorporation of coumarin along with azobenzene was prepared via esterification reaction and differ in the length of alkyl group, CnH2n+1, where n = 6, 8, 10, 12 and 14. Azo-coumarin bearing C14 alkyl chain shows Smectic–A phase while azo-coumarin bearing rest of long alkyl chain exhibited Nematic phase. The incorporation of natural product moieties into azobenzene network has increased electron delocalisation and liquid crystal properties. The photoswitching properties of said molecules were tested and the coumarin-azo compounds 3a-e took ~46 s to reach photostationary state during UV illumination and exhibited long thermal back relaxation time (~16 h) in solutions. Device is also fabricated to see the performance of the device with respect to the alkyl chain length. Presented studies show the importance of azo-coumarin derivatives with different chain length for the application of optical storage devices.

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