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1H-Pyrido[2,3-b]indole, 2,4-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50682-33-2

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50682-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50682-33-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,8 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 50682-33:
(7*5)+(6*0)+(5*6)+(4*8)+(3*2)+(2*3)+(1*3)=112
112 % 10 = 2
So 50682-33-2 is a valid CAS Registry Number.

50682-33-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-diphenyl-9H-pyrido[2,3-b]indole

1.2 Other means of identification

Product number -
Other names -

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:50682-33-2 SDS

50682-33-2Downstream Products

50682-33-2Relevant academic research and scientific papers

Synthesis of trifluoromethyl- A nd ester group-substituted α-carbolines via iron-catalyzed tandem cyclization reaction

Xu, Yumin,Chen, Xiaoqian,Gao, Yiqin,Yan, Zicong,Wan, Changfeng,Liu, Jin-Biao,Wang, Zhiyong

, p. 4354 - 4364 (2020/04/10)

An efficient approach to prepare trifluoromethyl-α-carbolines and ester group-substituted α-carbolines via the tandem cyclization reaction of 2-(2-aminophenyl)acetonitriles and trifluoromethyl 1,3-diones or ,?-unsaturated α-ketoesters was reported. The tr

OLED main body material, preparation method thereof, and OLED device

-

Paragraph 0073; 0074; 0077, (2019/12/02)

The invention discloses an OLED main body material, a preparation method thereof, and an OLED device. The structural formula of the OLED main body material is shown as a formula I; in the formula I, the R1 and R4 are one of C1-C20 alkyl, phenyl, 4-methylphenyl, 4-methoxyphenyl or furan-2-yl groups, the R2 and R3 are one of phenyl, naphthyl, furan, thiophene, benzofuran and benzothiophenol, and theR5, R6, R7 and R8 are one of C1-C20 alkyl, methoxy and phenyl groups. The OLED main body material provided by the invention is a main body material with better compatibility with an organic small molecule luminescent material, so that the problem of instability of a device caused by phase separation of a doping system is avoided, and the efficiency roll-off is relieved to prolong the service lifeof the device.

Preparation of Pyrido[2,3-b]indole Derivatives Using Silicates of Group 1 and 2 Metals

Sheikh, Setareh,Fazlinia, Abbas

, p. 2291 - 2296 (2018/09/06)

An efficient synthesis of 2,4-diaryl-9H-pyrido[2,3-b] indole derivatives in aqueous medium via the three-component reaction of indolin-2-one, a chalcone and ammonium acetate was developed using Na2SiO3, K2SiO3, Li2SiO3, CaSiO3, MgSiO3, BaSiO3, SrSiO3, and ZnSiO3 as catalysts. Results of activity evaluations indicated that among of the metal silicate used alkali metal silicates exhibits much higher activity than other samples due to the stronger basicity power and higher solubility in water. Under the optimum reaction conditions, all of the reactions with diverse aromatic aldehydes provided high yields in low reaction times.

Regioselective switching approach for the synthesis of α and δ carboline derivatives

Yang, Tang-Hao,Kuo, Chun-Wei,Kavala, Veerababurao,Konala, Ashok,Huang, Chia-Yu,Yao, Ching-Fa

, p. 1676 - 1679 (2017/02/10)

A metal-free protocol for accessing both α and δ-carboline derivatives, starting from a common indolylchalcone oxime ester precursor is reported. The reaction involves mild conditions and uses a regiodivergent approach. DDQ is used as a switching agent in selectively generating α and δ-carboline derivatives in good to moderate yields.

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