5-Isopropylaminoamylamine

Base Information

• Chemical Name: 5-Isopropylaminoamylamine
• CAS No.: 162713-22-6
• Molecular Formula: C₈H₂₀N₂
• Molecular Weight: 144.26
• Hs Code.: 2921290000
• DSSTox Substance ID: DTXSID30391256
• Wikidata: Q82188600
• Mol file: 162713-22-6.mol

Synonyms:5-Isopropylaminoamylamine;162713-22-6;N'-propan-2-ylpentane-1,5-diamine;5-(ISOPROPYLAMINO)AMYLAMINE;SCHEMBL3083438;DTXSID30391256;N-isopropyl-pentane-1,5-diamine;XBPAJDWNIXPXFJ-UHFFFAOYSA-N;N1-Isopropyl-pentane-1,5-diamine;(5-aminopentyl)(propan-2-yl)amine;AKOS013360722;EN300-6987874

Chemical Property of 5-Isopropylaminoamylamine

Chemical Property:

• Boiling Point: 78°C/ 8mm
• PSA: 38.05000
• LogP: 2.20460
• XLogP3: 0.7
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 6
• Exact Mass: 144.162648646
• Heavy Atom Count: 10
• Complexity: 62.3

Purity/Quality:

98%min ^*data from raw suppliers

5-Isopropylaminoamylamine 98% ^*data from reagent suppliers

Safty Information:

• Hazard Codes: C

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)NCCCCCN

Technology Process of 5-Isopropylaminoamylamine

There total 3 articles about 5-Isopropylaminoamylamine 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:

5-isopropylamino-valeronitrile → N-isopropylpiperidine (766-79-0) + N-isopropyl-pentanediyldiamine (162713-22-6)

Guidance literature:

With ammonia; nickel; at 100 ℃; Hydrogenation_.unter Druck;

DOI:10.1021/ja01641a045

Reference yield:

penta-2,4-dienenitrile (1615-70-9) → N-isopropyl-pentanediyldiamine (162713-22-6)

Guidance literature:

Multi-step reaction with 3 steps

1: Edukt₁ ist Gemisch der Stereoisomeren

2: palladium/charcoal; diethyl ether / Hydrogenation

3: Raney nickel; ethanolic ammonia / 100 °C / Hydrogenation_.unter Druck

With palladium on activated charcoal; diethyl ether; ammonia; nickel;

DOI:10.1021/ja01641a045

Reference yield:

5-isopropylamino-pent-3-enenitrile → N-isopropyl-pentanediyldiamine (162713-22-6)

Guidance literature:

Multi-step reaction with 2 steps

1: palladium/charcoal; diethyl ether / Hydrogenation

2: Raney nickel; ethanolic ammonia / 100 °C / Hydrogenation_.unter Druck

With palladium on activated charcoal; diethyl ether; ammonia; nickel;

DOI:10.1021/ja01641a045

upstream raw materials:

penta-2,4-dienenitrile