Pyrrolidine-1-carboximidamide

Base Information

• Chemical Name: Pyrrolidine-1-carboximidamide
• CAS No.: 13932-58-6
• Molecular Formula: C5H11 N3
• Molecular Weight: 113.162
• Hs Code.: 2933990090
• DSSTox Substance ID: DTXSID40383243
• Nikkaji Number: J60.125J
• Wikidata: Q82174894
• Mol file: 13932-58-6.mol

Synonyms:Pyrrolidine-1-carboximidamide;13932-58-6;Pyrrolidine-1-carboxamidine;1-Pyrrolidinecarboximidamide;pyrrolidine-1-carboximidine;1-Pyrrolidinecarboxamidine;SCHEMBL2878726;DTXSID40383243;PIGIRWPZTWLVLB-UHFFFAOYSA-N;MFCD05663369;AKOS000225411;BS-3741;EN300-53374;A922241

Chemical Property of Pyrrolidine-1-carboximidamide

Chemical Property:

• Boiling Point: 180.3°Cat760mmHg
• Flash Point: 62.8°C
• PSA: 53.11000
• Density: 1.27g/cm³
• LogP: 0.71360
• Storage Temp.: 2-8°C
• XLogP3: -0.1
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 113.095297364
• Heavy Atom Count: 8
• Complexity: 93.8

Purity/Quality:

97% ^*data from raw suppliers

Pyrrolidine-1-CarboximidamideHydrobromide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCN(C1)C(=N)N

Technology Process of Pyrrolidine-1-carboximidamide

There total 5 articles about Pyrrolidine-1-carboximidamide 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:

pyrrolidine-1-carboximidamide hydrochloride (49755-46-6) → 1-pyrrolidinecarboximidamide (13932-58-6)

Guidance literature:

With ethanol; sodium; at 20 ℃; for 0.5h;

DOI:10.1007/BF00798460

Reference yield:

pyrrolidine (123-75-1) + 3,5-dimethyl-1-pyrazolylformaminidium nitrate (38184-47-3) → 1-pyrrolidinecarboximidamide (13932-58-6)

Guidance literature:

DOI:10.1021/ja01112a051 DOI:10.1139/v58-225

Reference yield:

pyrrolidine (123-75-1) → 1-pyrrolidinecarboximidamide (13932-58-6)

Guidance literature:

With water;

upstream raw materials:

pyrrolidine

2-methylisothiourea sulphate

3,5-dimethyl-1-pyrazolylformaminidium nitrate

pyrrolidine-1-carboximidamide hydrochloride

Downstream raw materials:

2-(pyrrolidin-1-yl)-1H-benzimidazole

methyl-3-(amino(tetrahydro-1H-pyrrolyl)methylenesulfamoyl)-4-bromobenzoate