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3-(9H-Carbazole-9-yl)benzyl alcohol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

71935-22-3

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71935-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71935-22-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,9,3 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 71935-22:
(7*7)+(6*1)+(5*9)+(4*3)+(3*5)+(2*2)+(1*2)=133
133 % 10 = 3
So 71935-22-3 is a valid CAS Registry Number.

71935-22-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(9H-Carbazole-9-yl)benzyl alcohol

1.2 Other means of identification

Product number -
Other names 4-(9H-Carbazole-9-yl)benzyl alcohol

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:71935-22-3 SDS

71935-22-3Relevant academic research and scientific papers

Aggregation induced emission by pyridinium-pyridinium interactions

Leduskrasts, Kaspars,Suna, Edgars

, p. 460 - 465 (2019/01/16)

Non-covalent intermolecular interactions between pyridinium subunits in a crystal-state are an efficient means to accomplish aggregation induced emission and avoid aggregation caused quenching.

A carbazole fluorescent Thymus pyrimidine drug labeling reagents, synthesis and use (by machine translation)

-

Paragraph 0033; 0034; 0035, (2018/09/11)

The present invention relates to carbazole fluorescent Thymus pyrimidine drug labeling reagents, synthesis and application, in order to carbazole as fluorescent female ring, benzyl chloride as reaction active group, its chemical name is: 4 - (9 H - carbaz

EMISSIVE COMPOUNDS FOR ORGANIC LIGHT-EMITTING DIODES

-

Paragraph 0078; 0079, (2013/04/13)

Disclosed herein are compounds comprising an optionally substituted (2-phenylpyridinato-N,C2′)(2,4-pentanedionato)Pt(II). Some embodiments provide a light-emitting device, comprising: an anode layer; a cathode layer; and a light-emitting layer positioned

Synthesis, crystal structure and photoluminescence of phosphorescent copper (I) complexes containing hole-transporting carbazoly moiety

Yu, Tianzhi,Chai, Haifang,Zhao, Yuling,Zhang, Chengcheng,Liu, Peng,Fan, Duowang

, p. 179 - 185 (2013/06/27)

Two new mononuclear Cu(I) complexes based on 2-(2′-pyridyl) benzimidazolyl derivative ligand containing hole-transporting carbazole (L), [Cu(L)(DPEphos)](BF4) and [Cu(L)(PPh3)2] (BF4), where L = (4-(9H-carbazol-

Nonvolatile bistable resistive switching in a new polyimide bearing 9-phenyl-9H-carbazole pendant

Hu, Benlin,Zhuge, Fei,Zhu, Xiaojian,Peng, Shanshan,Chen, Xinxin,Pan, Liang,Yan, Qing,Li, Run-Wei

experimental part, p. 520 - 526 (2012/04/04)

A new polyimide bearing the functional pendant 9-phenyl-9H-carbazole moieties, poly[2,2-(4,4′-di(N-benzyloxycarbazole)-3,3′-biphenylene) propane-hexafluoroisopropylidenediphthalimide] (6F-BAHP-PC PI), has been designed as a functional material for resista

ASYMMETRIC ONE- AND TWO-PHOTON FLUOROPHORES FOR SIMULTANEOUS DETECTION OF MULTIPLE ANALYTES USING A COMMON EXCITATION SOURCE

-

Page/Page column sheet 3; 10, (2009/03/07)

A family of one- and two-photon dyes that have overlapping fluorescence excitation maxima between 365 nm and 425 nm and that are specifically functionalized for coupling to biomolecules. The dyes have defined Stokes shifts such that they produce a continuum of emission wavelengths. The dyes are asymmetrical bis stilbenes. The asymmetry of these dyes facilitates functionalization of the dyes with carboxyl, thiol, aldehyde-reactive or amine-reactive groups, which in turn facilitates coupling with macromolecules. Furthermore, the dyes of the present invention are photostable and have high quantum yields (fluorescence intensity).

Synthesis and photophysical properties of [60]fullerene adducts carrying oligocarbazole dendrons

Nakamura, Yosuke,Konno, Takashi,Watanabe, Satoru,Suzuki, Masato,Yoshihara, Toshitada,Tobita, Seiji,Nishimura, Jun

, p. 264 - 265 (2007/10/03)

[60]Fullerene adducts carrying oligocarbazole moieties were successfully prepared by the Bingel reactions. Their fluorescence spectra and transient absorption spectra suggested the intramolecular electron transfer from the oligocarbazole moiety to the ful

Antihypertensive compositions containing an aryl-substituted alanine azo and an arylhydrazino-propionic acid

-

, (2011/03/17)

Novel pharmaceutical compositions are disclosed. The compositions comprise an aryl substituted alanine and a substituted phenyl hydrazino propionic acid. The compositions are useful for treating hypertension.

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