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128542-54-1

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128542-54-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128542-54-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,5,4 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 128542-54:
(8*1)+(7*2)+(6*8)+(5*5)+(4*4)+(3*2)+(2*5)+(1*4)=131
131 % 10 = 1
So 128542-54-1 is a valid CAS Registry Number.

128542-54-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-iodonaphthalen-2-ol

1.2 Other means of identification

Product number -
Other names 1-iodo-6-hydroxynaphthalene

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:128542-54-1 SDS

128542-54-1Upstream product

128542-54-1Downstream Products

128542-54-1Relevant articles and documents

Synthesis of triarylamine-based alternating copolymers for polymeric solar cell

Lee, Jinhee,Cha, Hyojung,Kong, Hoyoul,Seo, Myungeun,Heo, Jaewon,Jung, In Hwan,Kim, Jisung,Shim, Hong-Ku,Park, Chan Eon,Kim, Sang Youl

, p. 4837 - 4845 (2014)

Two donor-acceptor alternating copolymers based on electron-rich triarylamine, di(1-(6-(2-ethylhexyl))naphthyl)phenylamine (DNPA), and electron-deficient benzothiadiazole and benzoselenadiazole derivatives were designed and synthesized via Suzuki coupling reaction. The resulting triarylamine-based alternating copolymers PDNPADTBT and PDNPADTBS showed good solubility in common organic solvents and good thermal stability. The optical band gaps determined from the onset absorption were 1.93 and 1.81 eV, respectively. By introducing the naphthalene ring into the triarylamine, copolymers had relatively deep HOMO energy levels of -5.48 and -5.45 eV, which led to a high open circuit voltage (Voc) and good air stability for photovoltaic application. Bulk heterojunction solar cells were fabricated with a structure of ITO/PEDOT-PSS/copolymers-PC70BM/LiF/Al by blending the copolymer with PC70BM. Both blend systems showed remarkably high Voc near 0.9 V, and the highest performance of 2.2% was obtained from PDNPADTBT, with Voc = 0.88 V, Jsc = 7.4 mA/cm2, and a fill factor of 34.4% under AM 1.5 G.

Antracene derivatives and organic light-emitting diode including the same

-

Paragraph 0280; 0281; 0282; 0283, (2016/10/10)

The present invention relates to an anthracene derivative and an organic light-emitting diode including the same and, more specifically, to a compound for an organic light-emitting diode represented by Chemical Formula A and an organic light-emitting diode including the same. [Chemical Formula A] In Chemical Formula A, R_1, R_2, m, n, and X_1 to X_7 are the same as described in the detailed description of the invention.COPYRIGHT KIPO 2015

Convergent synthesis of potent peptide inhibitors of the Grb2-SH2 domain by palladium catalyzed coupling of a terminal alkyne

Schoepfer, Joseph,Gay, Brigitte,End, Nicole,Muller, Evelyne,Scheffel, Gisela,Caravatti, Giorgio,Furet, Pascal

, p. 1201 - 1203 (2007/10/03)

A new strategy was developed to prepare in a very efficient and convergent manner C-terminal modified tripeptides with high affinities for the Grb2-SH2 domain. Using Pd(PPh3)2Cl2 as catalyst, selected naphthyl iodides and

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