8-Azaniumyloctanoate

Base Information

• Chemical Name: 8-Azaniumyloctanoate
• CAS No.: 1002-57-9
• Molecular Formula: C8H17NO2
• Molecular Weight: 159.228
• Hs Code.: 29224985
• Mol file: 1002-57-9.mol

Synonyms:

Chemical Property of 8-Azaniumyloctanoate

Chemical Property:

• Appearance/Colour: White to slightly beige crystalline powder
• Vapor Pressure: 0.000696mmHg at 25°C
• Melting Point: 194 °C (dec.)(lit.)
• Refractive Index: 1.468
• Boiling Point: 286 °C at 760 mmHg
• PKA: 4.76±0.10(Predicted)
• Flash Point: 126.8 °C
• PSA: 63.32000
• Density: 1.002 g/cm³
• LogP: 2.07060
• Storage Temp.: Store at 0-5°C
• Solubility.: Methanol (Very Slightly), Water (Slightly)
• Water Solubility.: Soluble in water.
• XLogP3: -2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 6
• Exact Mass: 159.125928785
• Heavy Atom Count: 11
• Complexity: 98.8

Purity/Quality:

99% ^*data from raw suppliers

8-Aminooctanoic acid ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 22-24/25-37/39-26

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: C(CCCC(=O)[O-])CCC[NH3+]
• Uses: 8-Aminooctanoic acid is involved in the preparation of lactams using enzyme catalyzed aminolysis.

Technology Process of 8-Azaniumyloctanoate

There total 26 articles about 8-Azaniumyloctanoate 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: 98.0%

2-azacyclononanone (935-30-8) → 8-Aminooctanoic acid (1002-57-9)

Guidance literature:

With hydrogenchloride; In water; for 2h; Heating;

Reference yield:

8-methoxycarbonylamino-octanoic acid methyl ester (82105-71-3) → 8-Aminooctanoic acid (1002-57-9)

Guidance literature:

With hydrogenchloride;

Reference yield:

8,8-dichloro-oct-7-enylamine (98551-63-4) → 8-Aminooctanoic acid (1002-57-9)

Guidance literature:

With sulfuric acid;

upstream raw materials:

8-methoxycarbonylamino-octanoic acid methyl ester

8,8-dichloro-oct-7-enylamine

7-Cyanoheptanoic acid

7-Cyan-2,5-heptadiensaeure

Downstream raw materials:

8-benzenesulfonylamino-octanoic acid

8-tert-butoxycarbonylaminooctanoic acid

8-aminooctanoic acid ethyl ester hydrochloride

8-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)octanoic acid

Refernces

• 1、 Jung, Hyunsang,Kim, Byung-Gee,Kim, Ye Chan,Park, Beom Gi,Patil, Mahesh D.,Sarak, Sharad,Yoo, Hee-Wang,Yun, Hyungdon. "Multi-enzymatic cascade reactions with Escherichia coli-based modules for synthesizing various bioplastic monomers from fatty acid methyl esters?". supporting information. p. 2222 - 2231. Retrieved 2022/04/03.
• 2、 Sung, Sihyong,Jeon, Hyunwoo,Sarak, Sharad,Ahsan, Md Murshidul,Patil, Mahesh D.,Kroutil, Wolfgang,Kim, Byung-Gee,Yun, Hyungdon. "Parallel anti-sense two-step cascade for alcohol amination leading to ω-amino fatty acids and α,ω-diamines". supporting information. p. 4591 - 4595. Retrieved 2018/10/23.