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198017-57-1

2-Amino-3-nitro-4-phenylpyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 198017-57-1 Structure

  • Basic information

    1. Product Name: 2-Amino-3-nitro-4-phenylpyridine
    2. Synonyms: 2-Amino-3-nitro-4-phenylpyridine
    3. CAS NO:198017-57-1
    4. Molecular Formula: C11H9N3O2
    5. Molecular Weight: 215.20806
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 198017-57-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 392.3±42.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.327±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 2.22±0.47(Predicted)
    10. CAS DataBase Reference: 2-Amino-3-nitro-4-phenylpyridine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-Amino-3-nitro-4-phenylpyridine(198017-57-1)
    12. EPA Substance Registry System: 2-Amino-3-nitro-4-phenylpyridine(198017-57-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 198017-57-1(Hazardous Substances Data)

198017-57-1 Usage

Chemical compound

2-Amino-3-nitro-4-phenylpyridine

Physical state

Yellow solid

Molecular weight

215.21 g/mol

Uses

Intermediate in the synthesis of pharmaceuticals and organic compounds

Potential

Building block for the creation of drugs and chemical products

Hazards

Toxic if ingested or inhaled, can cause skin and eye irritation

Storage

Cool, dry, well-ventilated area, away from ignition sources and incompatible materials

Check Digit Verification of cas no

The CAS Registry Mumber 198017-57-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,0,1 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 198017-57:
(8*1)+(7*9)+(6*8)+(5*0)+(4*1)+(3*7)+(2*5)+(1*7)=161
161 % 10 = 1
So 198017-57-1 is a valid CAS Registry Number.

198017-57-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-nitro-4-phenylpyridin-2-amine

1.2 Other means of identification

Product number -
Other names 2-Amino-3-nitro-4-phenylpyridine

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:198017-57-1 SDS

198017-57-1Downstream Products

198017-57-1Relevant articles and documents

TrkA KINASE INHIBITORS, COMPOSITIONS AND METHODS THEREOF

-

Page/Page column 35, (2016/10/31)

The present invention is directed to bicyclic heteroaryl benzamide compounds of formulas (I) which are tropomyosin-related kinase (Trk) family protein kinase inhibitors, and hence are useful in the treatment of pain, inflammation, cancer, restenosis, atherosclerosis, psoriasis, thrombosis, a disease, disorder, injury, or malfunction relating to dysmyelination or demyelination or a disease or disorder associated with abnormal activities of nerve growth factor (NGF) receptor TrkA.

Synthesis of 6-Phenyl-Atevirdine

Troschuetz, Reinhard,Karger, Alexander

, p. 1147 - 1151 (2007/10/03)

The synthesis of 6-phenyl-atevirdine (17), a lipophilic derivative of the potent HIV-1 reverse transcriptase inhibitor atevirdine (1), is described. The title compound was prepared from dithioacetale 2 via keteneaminal 4 and the nitropyridine derivative 10. Unexpectedly, no anti HIV activity was observed for the novel atevirdine derivative 17. The key intermediates 6, 8 and 10 could also be prepared from keteneaminal 18 via chloropyridines 22-24.

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