5-Bromoimidazo[1,2-a]pyridine hydrobromide

Base Information

• Chemical Name: 5-Bromoimidazo[1,2-a]pyridine hydrobromide
• CAS No.: 603301-13-9
• Molecular Formula: C7H6Br2N2
• Molecular Weight: 277.946
• Hs Code.: 2933990090
• DSSTox Substance ID: DTXSID50591953
• Mol file: 603301-13-9.mol

Synonyms:603301-13-9;5-Bromoimidazo[1,2-a]pyridine hydrobromide;5-Bromo-imidazo[1,2-a]pyridine HBr;5-Bromo-imidazo[1,2-a]pyridine hydrobromide;5-bromoimidazo[1,2-a]pyridine;hydrobromide;C7H6Br2N2;5-Bromoimidazo[1,2-a]pyridinehydrobromide;5-bromoimidazo[1,2-a]pyridine,hydrobromide;SCHEMBL2265015;DTXSID50591953;GAYMKIHDZOYBJX-UHFFFAOYSA-N;MFCD11053554;AKOS015998640;AS-36582;DA-18330;CS-0171506;5-Bromoimidazo[1,2-a]pyridine--hydrogen bromide (1/1);5-Bromo-imidazo[1 pound not2-a]pyridine hydrobromic acid

Chemical Property of 5-Bromoimidazo[1,2-a]pyridine hydrobromide

Chemical Property:

• PSA: 17.30000
• LogP: 3.05490
• Storage Temp.: Inert atmosphere,Room Temperature
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 277.88772
• Heavy Atom Count: 11
• Complexity: 129

Purity/Quality:

98%,99%, ^*data from raw suppliers

5-Bromo-imidazo[1,2-a]pyridineHydrobromide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC2=NC=CN2C(=C1)Br.Br

Technology Process of 5-Bromoimidazo[1,2-a]pyridine hydrobromide

There total 1 articles about 5-Bromoimidazo[1,2-a]pyridine hydrobromide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 81.0%

2-Amino-6-bromopyridine (19798-81-3,1184170-10-2) + Bromoacetaldehyde diethyl acetal (2032-35-1) → 5-bromoimidazo[1,2-a]pyridine hydrobromide (603301-13-9)

Guidance literature:

In butan-1-ol; Heating / reflux;

Reference yield: 100.0%

5-bromoimidazo[1,2-a]pyridine hydrobromide (603301-13-9) → 5-bromoimidazo<1,2-a>pyridine (69214-09-1)

Guidance literature:

With sodium hydrogencarbonate; In ethyl acetate;

upstream raw materials:

2-Amino-6-bromopyridine

Bromoacetaldehyde diethyl acetal

Downstream raw materials:

5-bromoimidazo<1,2-a>pyridine

Refernces

• 1、 -. "PURINE DERIVATIVES AS KINASE INHIBITORS". Page/Page column 39-40. . Retrieved 2008/06/13.