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65182-56-1

3-AMINO-2-CHLORO-6-(TRIFLUOROMETHYL)PYRIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 65182-56-1 Structure

  • Basic information

    1. Product Name: 3-AMINO-2-CHLORO-6-(TRIFLUOROMETHYL)PYRIDINE
    2. Synonyms: 2-(1,8-Naphthyridin-2-ly)phenol;2-(2-Hydroxyphenyl)-1,8-naphthyridine;Phenol,2-(1,8-naphthyridin-2-yl)-;STAT1 Enhancer, 2-NP
    3. CAS NO:65182-56-1
    4. Molecular Formula: C14H10N2O
    5. Molecular Weight: 196.56
    6. EINECS: N/A
    7. Product Categories: Inhibitors
    8. Mol File: 65182-56-1.mol

  • Chemical Properties

    1. Melting Point: 92-94°C
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: orange/
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: room temp
    8. Solubility: DMSO: ≥10mg/mL
    9. CAS DataBase Reference: 3-AMINO-2-CHLORO-6-(TRIFLUOROMETHYL)PYRIDINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-AMINO-2-CHLORO-6-(TRIFLUOROMETHYL)PYRIDINE(65182-56-1)
    11. EPA Substance Registry System: 3-AMINO-2-CHLORO-6-(TRIFLUOROMETHYL)PYRIDINE(65182-56-1)

  • Safety Data

    1. Hazard Codes: Xn,T
    2. Statements: 22-41-36-25
    3. Safety Statements: 26-39-45
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 65182-56-1(Hazardous Substances Data)

65182-56-1 Usage

Uses

2-(1,8-naphthyridin-2-yl)-Phenol is which selectively enhances STAT1 transcription activity.

Check Digit Verification of cas no

The CAS Registry Mumber 65182-56-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,8 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65182-56:
(7*6)+(6*5)+(5*1)+(4*8)+(3*2)+(2*5)+(1*6)=131
131 % 10 = 1
So 65182-56-1 is a valid CAS Registry Number.

65182-56-1 Well-known Company Product Price

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  • Detail

  • Sigma

  • (N2040)  2-NP  ≥98% (HPLC)

  • 65182-56-1

  • N2040-5MG

  • 724.23CNY

  • Detail

  • Sigma

  • (N2040)  2-NP  ≥98% (HPLC)

  • 65182-56-1

  • N2040-25MG

  • 2,925.00CNY

  • Detail

65182-56-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(1H-1,8-naphthyridin-2-ylidene)cyclohexa-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names 2-<o-Hydroxy-phenyl>-1,8-naphthyridin

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:65182-56-1 SDS

65182-56-1Relevant articles and documents

Half-sandwich d6 metal complexes comprising of 2-substituted-1,8-napthyridine ligands with unexpected bonding modes: Synthesis, structural and anti-cancer studies

Adhikari, Sanjay,Hussain, Omar,Phillips, Roger M.,Kollipara, Mohan Rao

, p. 27 - 37 (2018)

The Friedl?nder condensation reaction between 2-aminonicotinealdehyde and acetophenone derivatives in presence of potassium hydroxide yielded 2-substituted-1,8-napthyridine derivatives viz. 2-(1,8-napthyridin-2-yl)phenol (PHNp), 2-(1,8-napthyridin-2-yl)an

Friedlaender reaction of 3-acetyltropolones: Synthesis of naphthyridinyl- and allied heterocyclic-substituted tropolones

Piao, Ming-Zhu,Imafuku, Kimiaki

, p. 389 - 398 (1996)

Five 3-acetyltropolones reacted with 2-amino-3-pyridinecarbaldehyde to afford the corresponding 3-(1,8-naphtliyridin-2-yl)tropoIones in excellent yields. In a similar manner, 1,6-naphthyridin-2-yl-, 1,7-naphthyridin-2-yl-, 6-pyrido[2,3-&]pyrazinyl-, and 1

Microwave assisted synthesis of 1,8- naphthyridines

Mogilaiah,Reddy,Rao

, p. 837 - 838 (2007/10/03)

A highly efficient and practical methodology for the synthesis of 2-aryl-1.8-naphthyridines 3 is described starting from 2-aminonicotinaldehyde 1 and various acetophenones under microwave conditions.

Substituted 1,8-Naphthyridines: Part VI - Synthesis of 3-Aroyl-2-phenyl-1,8-naphthyridines

Rao, G. Rama,Mogilaiah, K.,Reddy, K. Rajendar,Sreenivasulu, B.

, p. 200 - 202 (2007/10/02)

The condensation of 2-aminonicotinaldehyde (1) with ω-benzoylacetophenones (2) leads to either 3-aroyl-2-phenyl-1,8-naphthyridines (3) in the presence of gl. acetic acid containing a catalytic amount of conc.H2SO4, or to 2-aryl-1,8-naphthyridines (4) in e

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