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1,2-Benzenediamine, 4,5-bis(dodecyloxy)is a chemical compound that belongs to the class of aromatic amines. It is a derivative of 1,2-benzenediamine, commonly known as o-phenylenediamine, with two dodecyloxy (C12H25O-) groups attached to the 4 and 5 positions of the benzene ring. 1,2-Benzenediamine, 4,5-bis(dodecyloxy)is characterized by its potential applications in various industries, despite its toxic and irritating properties that require careful handling.

190435-62-2

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190435-62-2 Usage

Uses

Used in Polymer and Material Production:
1,2-Benzenediamine, 4,5-bis(dodecyloxy)is used as a key component in the production of polymers and materials, particularly for the synthesis of dyes, pigments, and adhesives. Its unique structure allows for the creation of a wide range of products with diverse properties and applications.
Used in Pharmaceutical Manufacturing:
This chemical compound serves as an intermediate in the manufacture of pharmaceuticals, contributing to the development of various medications. Its presence in the production process highlights its importance in the synthesis of active pharmaceutical ingredients.
Used in Agricultural Chemical Production:
1,2-Benzenediamine, 4,5-bis(dodecyloxy)is also utilized in the production of agricultural chemicals, playing a crucial role in the synthesis of various agrochemicals that aid in crop protection and enhancement of agricultural yields.

Check Digit Verification of cas no

The CAS Registry Mumber 190435-62-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,4,3 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 190435-62:
(8*1)+(7*9)+(6*0)+(5*4)+(4*3)+(3*5)+(2*6)+(1*2)=132
132 % 10 = 2
So 190435-62-2 is a valid CAS Registry Number.

190435-62-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-didodecoxybenzene-1,2-diamine

1.2 Other means of identification

Product number -
Other names 1,2-Benzenediamine,4,5-bis(dodecyloxy)

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:190435-62-2 SDS

190435-62-2Relevant academic research and scientific papers

Room-temperature redox-active liquid crystals composed of tetraazanaphthacene derivatives

Isoda, Kyosuke,Abe, Tomonori,Tadokoro, Makoto

, p. 2951 - 2954 (2013)

Liquid-crystalline (LC) N-heteroacenes, tetraazanaphthacene (TANC), and fluoflavin (FFV) were synthesized, and their self-assembly into columnar LC structures at room temperature was investigated. LC TANC and LC FFV functioned as an electron acceptor and

Electrochromic π-Conjugated Copolymers Derived from Azulene, Fluorene, and Dialkyloxybenzothiadiazole

Lim, Shaun Zhi Hao,Neo, Wei Teng,Cho, Ching Mui,Wang, Xiaobai,Tan, Angeline Yan Xuan,Chan, Hardy Sze On,Xu, Jianwei

, p. 1048 - 1056 (2013/09/24)

A series of random π-conjugated copolymers P1, P2, and P3 were synthesised from 1,3-dibromoazulene, 4,7-dibromo-5,6-bis(dodecyloxy)benzo-2,1,3- thiadiazole, and 9,9-dioctylfluorene-2,7-bis(trimethyleneborate) via Suzuki coupling reactions. The copolymers

New octahedral, head-tail iron(II) complexes with spin crossover properties

Schlamp, Stephan,Thoma, Peter,Weber, Birgit

, p. 2759 - 2768 (2012/08/14)

The synthesis and characterisation of four new Schiff base-like ligands with long alkyl chains in the outer periphery and their iron(II) complexes with methanol and pyridine as axial ligands is reported. Two of the methanol complexes crystallise in a lipi

New moderate bandgap polymers containing alkoxysubstituted-benzo[c][1,2,5] thiadiazole and thiophene-based units

Lim, Zheng Bang,Xue, Bofei,Bomma, Swarnalatha,Li, Hairong,Sun, Shuangyong,Lam, Yeng Ming,Belcher, Warwick J.,Dastoor, Paul C.,Grimsdale, Andrew C.

, p. 4387 - 4397 (2012/05/20)

Alkoxysubstituted benzo[c][1,2,5]thiadiazole electron accepting units were prepared and copolymerized with various thiophene-based electron donating monomers to produce new low bandgap polymers P1-4. The materials showed broad absorption in the range from

Room temperature liquid crystalline perylene diester benzimidazoles with extended absorption

Wicklein, Andre,Muth, Mathis-Andreas,Thelakkat, Mukundan

, p. 8646 - 8652 (2011/06/09)

The synthesis, characterization and thermotropic properties of novel asymmetrically substituted discotic molecules, perylene diester benzimidazoles (PDBIs), are presented. PDBIs were designed with an imidazole unit at 3,4 positions and a bisester moiety a

Solvophobic control of core-substituted naphthalene diimide nanostructures

Bhosale, Sheshanath V.,Jani, Chintan,Lalander, Cecilia H.,Langford, Steven J.

supporting information; experimental part, p. 973 - 975 (2010/06/12)

The requirements for the self-assembly of 2,3-annulated core-substituted NDIs into discrete worm-like nanostructures are explored in MeOH-CHCl 3 solutions. AFM was used to visualize and characterize the structures formed at precise proportions

Synthesis and stereochemistry of long-chain quinoxaline metallocyclophanes

Howard, Mark J.,Heirtzler, Fenton R.,Dias, Sandra I. G.

, p. 2548 - 2553 (2008/09/19)

(Figure Presented) Condensation of 1,2-diamino-4,5-bis(n-alkoxy)arenes with an oligopyridyl-type α-diketone afforded a series of long-chain pyridine-quinoxaline hybrids. These were evaluated for their ability to self-assemble with tetrahedral Cu(I) and Ag

CHARGE-TRANSPORT MATERIALS, METHODS OF FABRICATION THEREOF, AND METHODS OF USE THEREOF

-

Page/Page column 83, (2008/06/13)

Briefly described, embodiments of this disclosure include charge-transport materials, methods of forming charge-transport materials, and methods of using the charge-transport materials.

In Situ Synthesis of Hexakis(alkoxy)diquinoxalino[2,3-a:2′,3′ -c]phenazines: Mesogenic Phase Transition of the Electron-Deficient Discotic Compounds

Ong, Chi Wi,Liao, Su-Chih,Chang, Tsu Hsing,Hsu, Hsiu-Fu

, p. 3181 - 3185 (2007/10/03)

2,3,8,9,14,15-Hexakis(alkoxy)diquinoxalino[2,3-a:2′,3′- c]phenazines with alkyl side chains varying from 6 to 12 carbon atoms were readily synthesized by the condensation of hexaketocyclohexane with the respective 1,2-bisalkoxy-4,5-diaminobenzene. Polariz

Neutral Anion Receptors: Synthesis and Evaluation as Sensing Molecules in Chemically Modified Field Effect Transistors

Antonisse, Martijn M. G.,Snellink-Ruel, Bianca H. M.,Yigit, Isteyfo,Engbersen, Johan F. J.,Reinhoudt, David N.

, p. 9034 - 9038 (2007/10/03)

A new class of anion selective receptors is based on the neutral uranylsalophene building block as Lewis acidic binding site. Additional hydrogen bond accepting or donating moieties near the anion binding site offer the possibility of varying the binding

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