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3-(trifluoromethyl)-5,6,7,8-tetrahydro-1,6-naphthyridine hydrochloride, with the CAS Number 209746-59-8, is an organic chemical compound belonging to the naphthyridine family, specifically to the tetrahydro-1,6-naphthyridines. It is characterized by the presence of a trifluoromethyl group and lacks common names. 3-(trifluoromethyl)-5,6,7,8-tetrahydro-1,6-naphthyridine hydrochloride's physical properties, such as boiling point, melting point, and density, may vary depending on storage or handling conditions. Its toxicity and safety measures should be obtained from the manufacturer or through scientific research. Primarily, it is utilized for scientific research purposes.

741736-95-8

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741736-95-8 Usage

Uses

Used in Scientific Research:
3-(trifluoromethyl)-5,6,7,8-tetrahydro-1,6-naphthyridine hydrochloride is used as a research chemical for [application reason]. The specific application reason is not provided in the materials, but it can be assumed that it is utilized in various experimental procedures and studies within the scientific community to explore its properties, potential reactions, or possible applications in different fields.
Since the provided materials do not specify different applications in various industries, no separate industry-specific uses can be listed based on the given information. Further research or details from the manufacturer would be required to identify specific applications beyond scientific research.

Check Digit Verification of cas no

The CAS Registry Mumber 741736-95-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,1,7,3 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 741736-95:
(8*7)+(7*4)+(6*1)+(5*7)+(4*3)+(3*6)+(2*9)+(1*5)=178
178 % 10 = 8
So 741736-95-8 is a valid CAS Registry Number.

741736-95-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(Trifluoromethyl)-5,6,7,8-tetrahydro-1,6-naphthyridine hydrochloride

1.2 Other means of identification

Product number -
Other names 3-(trifluoromethyl)-5,6,7,8-tetrahydro-1,6-naphthyridine,hydrochloride

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:741736-95-8 SDS

741736-95-8Relevant academic research and scientific papers

Spiroalkene carboxamide derivatives and their use as chemokine receptor modulators

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Page/Page column 52, (2012/10/18)

The present invention is directed to compounds of Formula (I) below, which are antagonists to the chemoattractant cytokine receptor 2 (CCR2), and/or 5 (CCR5), pharmaceutical compositions, and methods for use thereof.

SPIROALKENE CARBOXAMIDE DERIVATIVES AND THEIR USE AS CHEMOKINE RECEPTOR MODULATORS

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Page/Page column 63, (2012/10/18)

The present invention is directed to compounds of Formula (I) below, which are antagonists to the chemoattractant cytokine receptor 2 (CCR2), and/or 5 (CCR5), pharmaceutical compositions, and methods for use thereof.

CCR-2 ANTAGONIST SALT

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Page/Page column 11; 22-23, (2008/06/13)

The present invention provides an efficient synthesis for the preparation of ((1R,3S)-3-isopropyl-3-{[3-(trifluoromethyl)-7,8-dihydro-1,6-naphthyridin-6(5H)-yl]carbonyl}cyclopentyl)[(3S,4S)-3-m ethoxytetrahydro-2H-pyran-4-yl]amine and its succinate salt.

PROCESS FOR THE PREPARATION OF CCR-2 ANTAGONIST

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Page/Page column 10; 22-23, (2010/02/11)

The present invention provides an efficient synthesis for the preparation of ((1R,3S)-3-isopropyl-3- {[3-(trifluoromethyl)-7,8-dihydro-1,6-naphthyridin-6(5H)-yl]carbonyl} cyclopentyl)[(3S,4S)-3-m ethoxytetrahydro- 2H-pyran-4-yl]amine and its succinate sal

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