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34069-89-1

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34069-89-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34069-89-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,0,6 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 34069-89:
(7*3)+(6*4)+(5*0)+(4*6)+(3*9)+(2*8)+(1*9)=121
121 % 10 = 1
So 34069-89-1 is a valid CAS Registry Number.

34069-89-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 1,1'-diphenylamine-2,2'-dicarboxylate

1.2 Other means of identification

Product number -
Other names 2,2'-Dicarbomethoxy-diphenylamin

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:34069-89-1 SDS

34069-89-1Relevant articles and documents

Bis-aroylhydrazone based on 2,2′-bis substituted diphenylamine for synthesis of new binuclear organotin (IV) complexes: Spectroscopic characterization, crystal structures, in vitro DNA-binding, plasmid DNA cleavage, PCR and cytotoxicity against MCF7 cell

Sedaghat, Tahereh,Shafiei, Mohammad,Simpson, Jim,Yousefi, Maryam

, (2019)

New dinuclear organotin (IV) complexes, Me4Sn2L, Ph4Sn2L and Bu4Sn2L, have been synthesized from reaction of R2SnCl2 (R?=?Me, Ph and Bu) with a 2,2′-bis-substituted di

Organic light emitting device, carbonyl bridged triarylamine derivative and application of carbonyl bridged triarylamine derivative

-

Paragraph 0106; 0107; 0108, (2019/03/28)

The present invention relates to an organic light emitting device, a carbonyl bridged triarylamine derivative and application of the carbonyl bridged triarylamine derivative. The carbonyl bridged triarylamine derivative comprises compounds represented in

An Efficient Amphiphilic-Type Triphenylamine-Based Organic Hole Transport Material for High-Performance and Ambient-Stable Dopant-Free Perovskite and Organic Solar Cells

Reddy, Saripally Sudhaker,Park, Ho-Yeol,Kwon, Haeun,Shin, Jongmoon,Kim, Chang-Su,Song, Myungkwan,Jin, Sung-Ho

supporting information, p. 6426 - 6431 (2018/04/19)

A new set of simply structured triphenylamine-based small molecules are synthesized and evaluated as dopant-free hole transporting materials (HTMs) for high-performance perovskite solar cells (PSCs) and bulk heterojunction inverted organic solar cells (BHJ IOSCs). Surprisingly, the new amphiphilic-type HTM-1 (with internal hydrophilic groups and peripheral hydrophobic alkyl tails) showed better compatibility and performance than the actual target molecule, that is, HTM-2 in PSCs and BHJ IOSCs. Importantly, the HTM-1-based dopant-free PSCs and BHJ IOSCs exhibited high power conversion efficiencies (PCEs) of 11.45 % and 8.34 %, respectively. These performances are superior and comparable to those of standard HTMs Spiro-OMeTAD (2,2′,7,7′-tetrakis(N,N-di-p-methoxyphenylamine)-9,9′-spirobifluorene) and PEDOT:PSS (poly(3,4-ethylenedioxythiophene)/polystyrene sulfonate) in PSCs and BHJ IOSCs, respectively. The enhanced device performance of the HTM-1-based PSCs is ascribed to its strong affinity towards the perovskite, properly aligned energy levels with respect to the perovskite valence band, and excellent hole transporting behavior. In addition, the well-organized energy levels of the HTMs showed excellent compatibility in BHJ IOSCs. The new amphiphilic-type HTM-based photovoltaic devices also showed long-term air stability over 700 h. These promising results offer new and unexpected prospects for engineering the interface between the photoactive material and HTMs in PSCs and BHJ IOSCs.

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