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4-(Quinolin-8-yl)benzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

380359-19-3

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380359-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 380359-19-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,0,3,5 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 380359-19:
(8*3)+(7*8)+(6*0)+(5*3)+(4*5)+(3*9)+(2*1)+(1*9)=153
153 % 10 = 3
So 380359-19-3 is a valid CAS Registry Number.

380359-19-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-quinolin-8-ylbenzaldehyde

1.2 Other means of identification

Product number -
Other names 4-(QUINOLIN-8-YL)BENZALDEHYDE

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:380359-19-3 SDS

380359-19-3Downstream Products

380359-19-3Relevant academic research and scientific papers

Bathocuproine-Enabled Nickel-Catalyzed Selective Ullmann Cross-Coupling of Two sp 2-Hybridized Organohalides

Li, Yuqiang,Yin, Guoyin

supporting information, p. 1657 - 1661 (2021/09/13)

Cross-coupling reactions are essential for the synthesis of complex organic molecules. Here, we report a nickel-catalyzed Ullmann cross-coupling of two sp 2-hybridized organohalides, featuring high cross-selectivity when the two coupling partners are used in a 1:1 ratio. The high chemoselectivity is governed by the bathocuproine ligand. Moreover, the mild reductive reaction conditions allow that a wide range of functional groups are compatible in this Ullmann cross-coupling.

Pyridine-2-yl-aminoalkyl carbonyl glycyl-γ(b)-alanine and derivatives thereof

-

, (2008/06/13)

The invention relates to compounds of the formula I R1 is H, A, Ar, Hal, —OH, —O—A, —CF3 or —OCF3; R2 and R7 are H or A; R3 is R4, R5 and R6 are in each cas

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