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6-benzyl-2-(trifluoroMethyl)-5,6,7,8- tetrahydro-1,6-naphthyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1108192-98-8

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1108192-98-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1108192-98-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,8,1,9 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1108192-98:
(9*1)+(8*1)+(7*0)+(6*8)+(5*1)+(4*9)+(3*2)+(2*9)+(1*8)=138
138 % 10 = 8
So 1108192-98-8 is a valid CAS Registry Number.

1108192-98-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-benzyl-2-(trifluoromethyl)-7,8-dihydro-5H-1,6-naphthyridine

1.2 Other means of identification

Product number -
Other names 6-benzyl-2-(trifluoromethyl)-5,6,7,8-tetrahydro-1,6-naphthyridine

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:1108192-98-8 SDS

1108192-98-8Relevant academic research and scientific papers

Substituted amide compound and application

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Paragraph 0165; 0166; 0169; 0170, (2017/06/27)

The invention belongs to the field of agricultural bactericidal, insecticidal and acaricidal agents, and relates to a substituted amide compound and an application. The substituted amide compound has a structure as shown in a general formula I in the specification; and in the general formula I, substituents are defined in the specification. The compound provided by the invention has broad-spectrum bactericidal, insecticidal and acaricidal activities, has excellent control effects on diseases like cucumber downy mildew, corn rust, wheat powdery mildew and rice blast, especially has better control effects on the corn rust, also has excellent control effects on aphids and Tetranychus cinnabarinus, and especially can obtain good effects on the Tetranychus cinnabarinus at a low dosage.

Substituted tetrahydroisoquinoline compound and application

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Paragraph 0198; 0201; 0202, (2017/07/23)

The invention discloses a substituted tetrahydroisoquinoline compound and application. The compound has a structure as shown in a general formula I in the specification; and in the general formula I, substituents are defined in the specification. The comp

ANTI-PULMONARY TUBERCULOSIS NITROIMIDAZOLE DERIVATIVE

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Paragraph 0221; 0224; 0225, (2017/12/31)

Disclosed is a substituted nitroimidazole derivative, which is mainly used for treating related diseases caused by mycobacterial infections, such as Mycobacterium tuberculosis, especially being suitable for diseases caused by resistant Mycobacterium tuberculosis.

PYRAZOLOPYRIMIDINE DERIVATIVES USEFUL AS INHIBITORS OF BRUTON'S TYROSINE KINASE

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Paragraph 00583, (2014/12/12)

This invention relates to novel compounds. The compounds of the invention are tyrosine kinase inhibitors. Specifically, the compounds of the invention are useful as inhibitors of Bruton's tyrosine kinase (BTK). The invention also contemplates the use of the compounds for treating conditions treatable by the inhibition of Bruton's tyrosine kinase, for example cancer, lymphoma, leukemia and immunological diseases.

A concise one-pot synthesis of trifluoromethyl-containing 2,6-disubstituted 5,6,7,8-tetrahydroquinolines and 5,6,7,8-tetrahydronaphthyridines

Johnson, Russell J.,O'Mahony, Donogh J. R.,Edwards, William T.,Duncton, Matthew A. J.

, p. 1358 - 1366 (2013/05/09)

5,6,7,8-Tetrahydroquinolines and 5,6,7,8-tetrahydronaphthyridines with appended trifluoromethyl groups are valuable chemotypes in medicinal chemistry due to the presence of a partially-saturated bicyclic ring and metabolically-stable CF3 group. 1H NMR studies were used to optimize the preparation of such compounds, using a three-step/one-pot procedure, to provide novel 2,6-disubstitued derivatives with a tertiary-substituent. Racemic 2,6-disubstituted tetrahydroquinolines were separated by chiral HPLC to provide single enantiomers.

NAPHTHYRIDINE DERIVATIVES AS POTASSIUM CHANNEL MODULATORS

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Page/Page column 13; 14, (2009/03/07)

This invention provided compounds of formula (I), where W and Z are, independently, CH or N, and where other substituents are defined herein. Such compounds are potassium channel modulators. The invention also provides a composition comprising a pharmaceu

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