2-Amino-4-bromopyridine hydrochloride

Base Information

• Chemical Name: 2-Amino-4-bromopyridine hydrochloride
• CAS No.: 1001419-41-5
• Molecular Formula: C5H5BrN2.ClH
• Molecular Weight: 209.48
• DSSTox Substance ID: DTXSID10702669
• Mol file: 1001419-41-5.mol

Synonyms:1001419-41-5;4-bromopyridin-2-amine;hydrochloride;2-amino-4-bromopyridine hydrochloride;4-BROMOPYRIDIN-2-AMINE HYDROCHLORIDE;2-amino-4-bromo-pyridinehydrochloride;2-amino-4-bromopyridine HCl;DTXSID10702669;4-BROMOPYRIDIN-2-AMINEHYDROCHLORIDE;CS-0036116;4-Bromopyridin-2-amine--hydrogen chloride (1/1)

Chemical Property of 2-Amino-4-bromopyridine hydrochloride

Chemical Property:

• PSA: 38.91000
• LogP: 2.80950
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 207.94029
• Heavy Atom Count: 9
• Complexity: 76.8

Purity/Quality:

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

4-Bromopyridin-2-aminehydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CN=C(C=C1Br)N.Cl

Technology Process of 2-Amino-4-bromopyridine hydrochloride

There total 1 articles about 2-Amino-4-bromopyridine hydrochloride 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: 100.0%

(4-bromopyridin-2-yl)-carbamic acid tert-butyl ester (207799-10-8) → C5H5BrN2*ClH (1001419-41-5)

Guidance literature:

With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 20h;

Reference yield:

C15H19ClO3S + C5H5BrN2*ClH (1001419-41-5) → C20H23BrN2O3S (1001419-42-6)

Guidance literature:

With pyridine; In dichloromethane; at 20 ℃; for 2h;

upstream raw materials:

(4-bromopyridin-2-yl)-carbamic acid tert-butyl ester

Downstream raw materials:

C₂₀H₂₃BrN₂O₃S

Refernces