Decanamide

Base Information

• Chemical Name: Decanamide
• CAS No.: 2319-29-1
• Molecular Formula: C10H21 N O
• Molecular Weight: 171.283
• Hs Code.: 2924199090
• European Community (EC) Number: 219-029-7
• NSC Number: 57564
• UNII: N1468ZF07R
• DSSTox Substance ID: DTXSID801022380,DTXSID80867310
• Nikkaji Number: J7.871I
• Wikidata: Q5801030
• Metabolomics Workbench ID: 4495
• Mol file: 2319-29-1.mol

Synonyms:Decanamide;2319-29-1;n-Decanamide;Capramide;Decan-1-amide;Decylamide;Decanoic acid amide;Decanamide-;UNII-N1468ZF07R;N1468ZF07R;EINECS 219-029-7;NSC-57564;67700-97-4;Decanoylamide;Capric acid amide;ARMID 10;SCHEMBL43639;SCHEMBL19407773;CHEBI:38833;DTXSID80867310;DTXSID801022380;CAA31929;NSC57564;EINECS 266-921-7;LMFA08010005;MFCD00025541;NSC 57564;AKOS009159490;AS-56239;CS-0133974;FT-0624486;D89393;A878311;Q5801030

Chemical Property of Decanamide

Chemical Property:

• Vapor Pressure: 0.000836mmHg at 25°C
• Melting Point: 98
• Refractive Index: 1.4621
• Boiling Point: 305.2°Cat760mmHg
• PKA: 16.63±0.40(Predicted)
• Flash Point: 138.4°C
• PSA: 43.09000
• Density: 0.881g/cm³
• LogP: 3.31270
• Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
• XLogP3: 3.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 8
• Exact Mass: 171.162314293
• Heavy Atom Count: 12
• Complexity: 112

Purity/Quality:

98%,99%, ^*data from raw suppliers

Decanamide >98.0%(GC) ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xn
• Statements: 22-37/38
• Safety Statements: 22-24/25-36/37

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: UVCB
• Canonical SMILES: CCCCCCCCCC(=O)N

Technology Process of Decanamide

There total 27 articles about Decanamide 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: 96.0%

N-t-butyloxycarbonyl-alanine-N'-hydroxysuccinimide ester (73488-76-3) + 1-aminodecane (2016-57-1) → decanamide (2319-29-1)

Guidance literature:

P₂ O₅; In N-methyl-acetamide;

Reference yield: 85.0%

1-decanoylpiperidine-2,6-dione → decanamide (2319-29-1)

Guidance literature:

With lithium hydroxide monohydrate; In water; at 20 ℃; for 2h;

DOI:10.1021/acs.orglett.1c00010

Reference yield: 81.0%

1-decanoic acid (334-48-5) → decanamide (2319-29-1)

Guidance literature:

1-decanoic acid; With thionyl chloride; In tetrahydrofuran; at 50 ℃; for 1h;

With ammonium hydroxide; In tetrahydrofuran; at 0 ℃; for 0.0833333h;

DOI:10.1021/acs.orglett.8b02422

upstream raw materials:

decylthiol

1,1-Dimethylurea

1-decanoic acid

n-decanenitrile

Downstream raw materials:

n-Nonylamin

1-aminodecane

n-decanenitrile

didecylamine

Refernces

• 1、 Gritter,Woosley. "". . p. 5544. Retrieved 1963.
• 2、 Govindan, Karthick,Chen, Nian-Qi,Chuang, Yu-Wei,Lin, Wei-Yu. "Unlocking Amides through Selective C–N Bond Cleavage: Allyl Bromide-Mediated Divergent Synthesis of Nitrogen-Containing Functional Groups". supporting information. p. 9419 - 9424. Retrieved 2021/11/30.
• 3、 Marchetti, Piera M.,Richardson, Shona M.,Kariem, Noor M.,Campopiano, Dominic J.. "Synthesis of: N-acyl amide natural products using a versatile adenylating biocatalyst". supporting information. p. 1192 - 1196. Retrieved 2019/07/31.