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8-Quinolinamine, N-8-quinolinyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88783-63-5

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88783-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88783-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,8 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 88783-63:
(7*8)+(6*8)+(5*7)+(4*8)+(3*3)+(2*6)+(1*3)=195
195 % 10 = 5
So 88783-63-5 is a valid CAS Registry Number.

88783-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-quinolin-8-ylquinolin-8-amine

1.2 Other means of identification

Product number -
Other names bis(quinolin-8-yl)amine

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:88783-63-5 SDS

88783-63-5Upstream product

88783-63-5Relevant academic research and scientific papers

Palladium-Catalyzed Synthesis of N-Cyclohexyl Anilines from Phenols with Hydrazine or Hydroxylamine via N-N/O Cleavage

Li, Jiang-Sheng,Qiu, Zihang,Li, Chao-Jun

, p. 3648 - 3653 (2017)

Direct access to amines from biomass-based phenols via deoxygenative transformation remains greatly challenging in organic synthesis. Herein, we present a palladium-catalyzed deoxygenative amination of phenols (and their benzyl ether) with hydrazine as nitrogen source. The hydroxylamine/formic acid can be substituted for hydrazine in some cases. This deoxyamination features the involvement of a complex C?O bond and N?N/O bond-cleavage process and allows for the construction of N-substituted cyclohexyl anilines from an array of phenols by finely controlling the reaction conditions in moderate to good yields. (Figure presented.).

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