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5-METHOXYQUINOLIN-6-AMINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54620-48-3

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54620-48-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54620-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,2 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54620-48:
(7*5)+(6*4)+(5*6)+(4*2)+(3*0)+(2*4)+(1*8)=113
113 % 10 = 3
So 54620-48-3 is a valid CAS Registry Number.

54620-48-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methoxyquinolin-6-amine

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:54620-48-3 SDS

54620-48-3Downstream Products

54620-48-3Relevant academic research and scientific papers

Synthesis of Aryl Amine Derivatives from Benzyl Nitriles via Electrocyclization of in Situ Generated N-Silyl Ketene Imines

Yoshimura, Fumihiko,Abe, Taiki,Tanino, Keiji

supporting information, p. 1630 - 1633 (2016/04/26)

The previously unexplored reactivity of N-silyl ketene imines in organic synthesis is reported. Benzyl nitriles containing an alkenyl or aryl group at the ortho position were smoothly converted into aryl amines in good yields under two sets of mild silyla

Synthesis of mono-substituted derivatives of 6-aminoquinoline

Lan, Tian,Yuan, Xian Xia,Yu, Jiang Hong,Jia, Chao,Wang, Yu Shi,Zhang, Hui Juan,Ma, Zi Feng,Ye, Wei Dong

scheme or table, p. 253 - 255 (2012/01/04)

Several 6-aminoquinoline derivatives, which could be used in drug design, have been synthesized. The reaction conditions were comparatively studied, and the p-chloroaniline was used as optimum oxidant in Skraup-Doebner-Von Miller reaction. The nitro group was reduced effectively by SnCl2 with no halo-removed occurred.

PHOTOLYSIS OF QUINOLYL AND ISOQUINOLYL AZIDES IN ALCOHOLS CONTAINING SULFURIC ACID

Sawanishi, Hiroyuki,Hirai, Toyoko,Tsuchiya, Takashi

, p. 2071 - 2074 (2007/10/02)

Photolysis of 3-azidoquinoline, 4-azidoisoquinoline, and 4-azidoquinoline N-oxide in alcohols containing sulfuric acid gave the corresponding α-alkoxy amino compounds (2,3,5,7) via nitrenium ion intermediates.In contrast, 3-azidoquinoline N-oxide, 5-azido and 8-azidoquinoline, and 5-azidoquinoline, upon irradiation under similar conditions, gave the different type of α-alkoxy amino compounds such as 9 and 13 via azirine or azacycloheptatetraene intermediates.

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