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Carbamic acid, [4-[(diphenylmethylene)amino]phenyl]phenyl-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

535960-10-2

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535960-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 535960-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,5,9,6 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 535960-10:
(8*5)+(7*3)+(6*5)+(5*9)+(4*6)+(3*0)+(2*1)+(1*0)=162
162 % 10 = 2
So 535960-10-2 is a valid CAS Registry Number.

535960-10-2SDS

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 N-(diphenylmethylene)-N'-(tert-butoxycarbonyl)-N'-(phenyl)-p-phenylenediamine

1.2 Other means of identification

Product number -
Other names tert-butyl (4-((diphenylmethylene)amino)phenyl)(phenyl)carbamate

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:535960-10-2 SDS

535960-10-2Relevant academic research and scientific papers

Thermally Activated Delayed Fluorescent Donor-Acceptor-Donor-Acceptor π-Conjugated Macrocycle for Organic Light-Emitting Diodes

Izumi, Saika,Higginbotham, Heather F.,Nyga, Aleksandra,Stachelek, Patrycja,Tohnai, Norimitsu,Silva, Piotr De,Data, Przemyslaw,Takeda, Youhei,Minakata, Satoshi

supporting information, p. 1482 - 1491 (2020/02/04)

A new class of thermally activated delayed fluorescent donor-acceptor-donor-acceptor (D-A-D-A) π-conjugated macrocycle comprised of two U-shaped electron-acceptors (dibenzo[a,j]phenazine) and two electron-donors (N,N′-diphenyl-p-phenyelendiamine) has been

Self-Assembly of a Functional Oligo(Aniline)-Based Amphiphile into Helical Conductive Nanowires

Bell, O. Alexander,Wu, Guanglu,Haataja, Johannes S.,Br?mmel, Felicitas,Fey, Natalie,Seddon, Annela M.,Harniman, Robert L.,Richardson, Robert M.,Ikkala, Olli,Zhang, Xi,Faul, Charl F. J.

, p. 14288 - 14294 (2015/11/28)

A tetra(aniline)-based cationic amphiphile, TANI-NHC(O)C5H10N(CH3)3+Br- (TANI-PTAB) was synthesized, and its emeraldine base (EB) state was found to self-assemble into nanowires in aqueous

Oligoaniline-Functionalized terpyridine ligands and their ruthenium(II) complexes: Synthesis, spectroscopic property and redox behavior

Qiu, Dongfang,Cheng, Yanxiang,Wang, Lixiang

scheme or table, p. 3247 - 3261 (2009/08/08)

A series of oligoaniline-functionalized mono- and bis-topic terpyridine ligands, i.e. C6H5[N(R)C6H4] nTPY (R = H, butyl, tert-butyloxycarbonyl; n = 1-4; TPY = 2,2′:6′,2″-terpyridyl) and TPYC6H 4[N(R)C6H4]mTPY (R = H, tert-butyloxycarbonyl; m = 2, 4), and the corresponding mono- and bis-nuclear ruthenium(II) complexes have been synthesized and verified. The spectroscopic results indicate that two kinds of π-π* transitions from TPY and oligoaniline fragments of ligands strongly shift to lower energy, and the metal-to-ligand charge-transfer transition (1MLCT) bands of all obtained complexes are considerably red-shifted (Δλmax = 22-64 nm) and their intensities become much more intense (approximately 4-6 times), compared with those of the reported complex [Ru(TPY)2] 2+. Moreover, the spectroscopic properties of the ligands and complexes with longer oligoaniline units (n = 3, 4) are markedly influenced by the external stimulus, such as the oxidation and proton acid doping. The characteristic absorption bands in the visual and near infrared (NIR) scales demonstrate the presence of various oxidized and doped states of the oligoaniline unit. All complexes show multiplicate redox processes based on metal center, oligoaniline and terpyridine units. The potential shifts suggest the donor and acceptor (D-A) interaction between the oligoaniline unit and the bis(terpyridine)-Ru2+ center.

Preparation and properties of poly(methacrylamide)s containing oligoaniline side chains

Chen, Ru,Benicewicz, Brian C.

, p. 6333 - 6339 (2007/10/03)

New poly(methacrylamide)s containing oligoaniline side chains were synthesized and characterized. Oligoanilines were prepared by palladium-catalyzed amination, followed by reaction with methacryloyl chloride to give methacrylamide monomers. Polymers were

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