7-Azaniumylheptanoate

Base Information

• Chemical Name: 7-Azaniumylheptanoate
• CAS No.: 929-17-9
• Molecular Formula: C7H15NO2
• Molecular Weight: 145.202
• Hs Code.: 2922499990
• Mol file: 929-17-9.mol

Synonyms:

Chemical Property of 7-Azaniumylheptanoate

Chemical Property:

• Vapor Pressure: 0.0019mmHg at 25°C
• Melting Point: 192-195 °C(lit.)
• Refractive Index: 1.467
• Boiling Point: 270.6 °C at 760 mmHg
• PKA: pK1: 4.502 (25°C)
• Flash Point: 117.5 °C
• PSA: 63.32000
• Density: 1.019 g/cm³
• LogP: 1.68050
• Storage Temp.: Store at RT.
• Water Solubility.: Soluble in water
• XLogP3: -2.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• Exact Mass: 145.110278721
• Heavy Atom Count: 10
• Complexity: 88.1

Purity/Quality:

99.9% ^*data from raw suppliers

7-Aminoheptanoic Acid ^*data from reagent suppliers

Safty Information:

• Safety Statements: 22-24/25

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(CCC[NH3+])CCC(=O)[O-]

Technology Process of 7-Azaniumylheptanoate

There total 33 articles about 7-Azaniumylheptanoate 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%

7-amino-heptanoic acid lactam (673-66-5) → 7-aminoheptanoic acid (929-17-9)

Guidance literature:

With hydrogenchloride;

DOI:10.1016/S0960-894X(97)00335-1

Reference yield: 99.0%

7-bromoheptanoic acid (30515-28-7) → 7-aminoheptanoic acid (929-17-9)

Guidance literature:

With ammonium hydroxide; In water; at 20 ℃;

DOI:10.1021/jm801072v

Reference yield: 93.0%

7-amino-heptanoic acid lactam (673-66-5) + barium(II) hydroxide → 7-aminoheptanoic acid (929-17-9)

Guidance literature:

7-amino-heptanoic acid lactam; barium(II) hydroxide; With water; at 110 ℃; for 6h;

With carbon dioxide; In water; for 0.333333h; Cooling with ice;

upstream raw materials:

7-amino-heptanoic acid lactam

7-aminoheptanenitrile

7-chloroheptanoic acid

7-amino-heptanoic acid isopropyl ester

Downstream raw materials:

7-amino-heptanoic acid lactam

heptanedioic acid

7-benzenesulfonylamino-heptanoic acid

methyl 7-aminoheptanoate hydrochloride

Refernces

• 1、 -. "MATERIALS AND METHODS OF PRODUCING 7-CARBON MONOMERS". Page/Page column 51; 52. . Retrieved 2016/07/27.
• 2、 -. "REVERSE AMIDE COMPOUNDS AS PROTEIN DEACETYLASE INHIBITORS AND METHODS OF USE THEREOF". . . Retrieved 2011/08/08.