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4-butoxyquinolin-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52176-33-7

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52176-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52176-33-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,1,7 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52176-33:
(7*5)+(6*2)+(5*1)+(4*7)+(3*6)+(2*3)+(1*3)=107
107 % 10 = 7
So 52176-33-7 is a valid CAS Registry Number.

52176-33-7SDS

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 4-butoxyquinolin-2-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:52176-33-7 SDS

52176-33-7Downstream Products

52176-33-7Relevant academic research and scientific papers

TOLL-LIKE RECEPTOR 8 AGONISTS

-

, (2015/07/07)

Compounds described herein can be used for therapeutic purposes. The compounds can be TLR agonists, such as TLR8 agonists. The compounds can be included in pharmaceutical compositions and used for therapies were being a TLR8 agonist is useful. The pharmac

Structure-based design of novel human toll-like receptor 8 agonists

Kokatla, Hari Prasad,Sil, Diptesh,Tanji, Hiromi,Ohto, Umeharu,Malladi, Subbalakshmi S.,Fox, Lauren M.,Shimizu, Toshiyoki,David, Sunil A.

, p. 719 - 723 (2014/05/06)

Toll-like receptor (TLR)-8 agonists activate adaptive immune responses by inducing robust production of T helper 1-polarizing cytokines, suggesting that TLR8-active compounds might be promising candidate vaccine adjuvants. Recently, a C2-butyl furo[2,3-c]

Antimicrobial 2 amino 4 alkoxyquinolines: synthesis and analysis of structure activity correlations

Actor,Berkoff,Craig,Julius,Redl,Grout,Hynam,Partridge

, p. 8 - 11 (2007/10/04)

The synthesis and in vitro antimicrobial activity of 28 2 amino 4 alkoxyquinolines against 4 species of Gram positive and 4 species of Gram negative bacteria and 4 species of fungi are reported. For the analysis of structure activity correlations the Free Wilson (FW) approach was explored but the nature of the data did not meet the requirements considered mandatory for a meaningful application of the FW method. Composite activities against the 3 different classes of microorganisms indicate that optimal activity rests primarily on the nature of the alkyl group at the 4 alkoxy position, where increasing chain length leads to increasing activity against Gram positive bacteria and fungi. The level of activity against Gram negative bacteria is too low for meaningful trends to be observed. Alkylation or acylation of the 2 amino group and substitution at the 3 position are detrimental to activity against all 3 classes of organisms.

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