5-Bromo-2-chloropyridine-4-carbaldehyde

Base Information

• Chemical Name: 5-Bromo-2-chloropyridine-4-carbaldehyde
• CAS No.: 1060802-23-4
• Molecular Formula: C₆H₃BrClNO
• Molecular Weight: 220.453
• Hs Code.: 2933399090
• European Community (EC) Number: 800-831-6
• DSSTox Substance ID: DTXSID00697414
• Wikidata: Q72453413
• Mol file: 1060802-23-4.mol

Synonyms:1060802-23-4;5-BROMO-2-CHLOROISONICOTINALDEHYDE;5-Bromo-2-chloropyridine-4-carbaldehyde;5-bromo-2-chloro-pyridine-4-carbaldehyde;MFCD11847346;5-BROMO-2-CHLORO-4-PYRIDINECARBOXALDEHYDE;5-BROMO-2-CHLOROPYRIDINE-4-CARBOXALDEHYDE;SCHEMBL9938111;DTXSID00697414;MAGFXBKNQAAQQA-UHFFFAOYSA-N;BCP06090;BBL102254;STL556053;AKOS005259975;DH-0700;PB13444;SY020938;CS-0039821;FT-0683961;EN300-313061;P11217;5-Bromo-2-chloropyridine-4-carboxaldehyde, 97%

Chemical Property of 5-Bromo-2-chloropyridine-4-carbaldehyde

Chemical Property:

• Melting Point: 63-68°C
• Boiling Point: 274℃
• PKA: -3.62±0.10(Predicted)
• Flash Point: 120℃
• PSA: 29.96000
• Density: 1.800
• LogP: 2.31000
• Storage Temp.: ?20°C
• XLogP3: 2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 218.90865
• Heavy Atom Count: 10
• Complexity: 133

Purity/Quality:

99%, ^*data from raw suppliers

5-Bromo-2-chloroisonicotinaldehyde ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T
• Hazard Codes: T
• Statements: 25-36/37/38
• Safety Statements: 26-45

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=C(C(=CN=C1Cl)Br)C=O

Technology Process of 5-Bromo-2-chloropyridine-4-carbaldehyde

There total 1 articles about 5-Bromo-2-chloropyridine-4-carbaldehyde 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: 85.0%

5-bromo-2-chloropyridine (53939-30-3) + N,N-dimethyl-formamide (68-12-2,33513-42-7) → 5-bromo-2-chloropyridine-4-carboxaldehyde (1060802-23-4)

Guidance literature:

5-bromo-2-chloropyridine; With n-butyllithium; diisopropylamine; In tetrahydrofuran; hexane; at -78 ℃; for 0.5h;

N,N-dimethyl-formamide; In tetrahydrofuran; hexane; at -60 ℃; for 0.5h;

Reference yield: 89.0%

5-bromo-2-chloropyridine-4-carboxaldehyde (1060802-23-4) + N-(benzyloxycarbonyl)phosphonoglycine trimethyl ester (100945-15-1,88568-95-0) → 1-benzyl 2-methyl 5-chloro-1H-pyrrolo[2,3-c]pyridine-1,2-dicarboxylate

Guidance literature:

With [2,2]bipyridinyl; potassium phosphate; copper(l) iodide; In dichloromethane; at 20 ℃; Inert atmosphere;

DOI:10.1039/c5ob00528k

Reference yield:

5-bromo-2-chloropyridine-4-carboxaldehyde (1060802-23-4) → 5-bromo-2-chloro-4-((3,4-dichlorophenoxy)methyl)pyridine

Guidance literature:

Multi-step reaction with 2 steps

1.1: sodium tetrahydroborate / methanol / 1.5 h / 20 °C

2.1: N-ethyl-N,N-diisopropylamine; methanesulfonyl chloride / tetrahydrofuran / 1.5 h / 0 °C

2.2: 17 h / 20 °C

With sodium tetrahydroborate; methanesulfonyl chloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol;

upstream raw materials:

5-bromo-2-chloropyridine

N,N-dimethyl-formamide

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