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3323-01-1

2-(p-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyridine is a complex organic chemical compound with the molecular formula C14H8N4O3. It is a derivative of imidazo[1,2-a]pyridine, which is a heterocyclic compound with a fused imidazole and pyridine ring system. The compound features a nitroso group (-N=O) at the 3-position and a p-nitrophenyl group (a phenyl ring with a nitro group at the para position) at the 2-position. 2-(p-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyridine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the preparation of other organic compounds. Due to its complex structure and functional groups, it is important to handle this chemical with care, as it may have potential health and environmental impacts.

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  • 3323-01-1 Structure

  • Basic information

    1. Product Name: 2-(p-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyridine
    2. Synonyms: 2-(p-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyridine
    3. CAS NO:3323-01-1
    4. Molecular Formula: C13H8N4O3
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 3323-01-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.49g/cm3
    6. Refractive Index: 1.727
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(p-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(p-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyridine(3323-01-1)
    11. EPA Substance Registry System: 2-(p-Nitrophenyl)-3-nitrosoimidazo[1,2-a]pyridine(3323-01-1)

  • 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: 3323-01-1(Hazardous Substances Data)

3323-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3323-01-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,2 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3323-01:
(6*3)+(5*3)+(4*2)+(3*3)+(2*0)+(1*1)=51
51 % 10 = 1
So 3323-01-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H8N4O3/c18-15-13-12(14-11-3-1-2-8-16(11)13)9-4-6-10(7-5-9)17(19)20/h1-8H

3323-01-1SDS

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 2-(4-nitrophenyl)-3-nitrosoimidazo[1,2-a]pyridine

1.2 Other means of identification

Product number -
Other names 2-<4-Nitro-phenyl>-3-nitroso-imidazo<1.2-a>pyridin

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:3323-01-1 SDS

3323-01-1Relevant articles and documents

NaNO2/I2-Mediated Regioselective Synthesis of Nitrosoimidazoheterocycles from Acetophenones by a Domino Process

Mukhopadhyay, Sushobhan,Dighe, Shashikant U.,Kolle, Shivalinga,Shukla, Praveen K.,Batra, Sanjay

, p. 3836 - 3844 (2016/08/16)

A regioselective synthesis of nitrosoimidazoheterocycles from the reaction of 2-aminopyridines and acetophenones in the presence of NaNO2and I2is described. The reaction is suggested to proceed by a domino process involving sequentia

Influence of the 2-aryl group on the ipso electrophilic substitution process of 2-arylimidazo[1,2-a]pyridines

Salgado-Zamora, Hector,Velazquez, Manuel,Mejia, Daniel,Campos-Aldrete,Jimenez, Rogelio,Cervantes, Humberto

, p. 27 - 32 (2008/09/19)

A systematic study of electrophilic substitution reactions of 3-nitroso-2-arylimidazo[1,2-a]pyridine confirmed that the nitroso group may be ipso-substituted by bromine (NBS in DMF) and that bromine in turn may be substituted by the nitroso group. Electro

Convenient Synthesis of Fused Heterocycles from α-Ketohydroximoyl Chlorides and Heterocyclic Amines

Parkanyi, Cyril,Abdelhamid, Abdou O.,Cheng, John C. S.

, p. 1029 - 1032 (2007/10/02)

Nitroso derivatives of imidazopyridine (11,13,14), imidazopyrimidine (15), imidazopyrazine (16), imidazopyrazole (17), and imidazo-1,2,4-triazole (19) were obtained in good yields from α-ketohydroximoyl chlorides 3 and 2-aminopyrazines (4-6), 2-aminopyrimidine (7), 2-aminopyrazine (8), 5-amino-3-phenylpyrazole (9), and 3-amino-2H-1,2,4-triazole (10), respectively.Under different conditions, the reaction of 3 with 3-amino-2H-1,2,4-triazole (10) and 2-aminopyrazine (8) afforded the noncyclized substitution products 18 and 22, respectively.The structures of the products were assigned and confirmed on the basis of their elemental analyses, spectral data, and alternate synthesis wherever possible.

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