Benzamide, 5-(acetylamino)-N-butyl-2-[(3-methyl-2-butenyl)oxy]-

Base Information

Chemical Name:Benzamide, 5-(acetylamino)-N-butyl-2-[(3-methyl-2-butenyl)oxy]-
CAS No.:400039-29-4
Molecular Formula:C18H26N2O3
Molecular Weight:318.416
Hs Code.:
DSSTox Substance ID:DTXSID70456358

Synonyms:400039-29-4;Benzamide, 5-(acetylamino)-N-butyl-2-[(3-methyl-2-butenyl)oxy]-;DTXSID70456358

Suppliers and Price of Benzamide, 5-(acetylamino)-N-butyl-2-[(3-methyl-2-butenyl)oxy]-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Benzamide, 5-(acetylamino)-N-butyl-2-[(3-methyl-2-butenyl)oxy]-

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:8
Exact Mass:318.19434270
Heavy Atom Count:23
Complexity:417

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCNC(=O)C1=C(C=CC(=C1)NC(=O)C)OCC=C(C)C

Technology Process of Benzamide, 5-(acetylamino)-N-butyl-2-[(3-methyl-2-butenyl)oxy]-

There total 3 articles about Benzamide, 5-(acetylamino)-N-butyl-2-[(3-methyl-2-butenyl)oxy]- 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: 80.0%

: 6382-44-1
5-acetamido-N-butylsalicylamide

: 870-63-3
prenyl bromide

: 400039-29-4
5-acetylamino-N-butyl-2-(3-methyl-but-2-enyloxy)-benzamide

Guidance literature:: With sodium isopropylate; In isopropyl alcohol; Heating;
DOI:10.1016/S0223-5234(01)01251-X

Reference yield:

: 89-57-6
5-Aminosalicylic Acid

: 400039-29-4
5-acetylamino-N-butyl-2-(3-methyl-but-2-enyloxy)-benzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: 79 percent / H₂O / 0.25 h / 50 °C

2.1: 1-hydroxybenzotriazole; N,N'-dicyclohexylcarbodiimide / dimethylformamide / 0.5 h / 0 °C

2.2: 86 percent / dimethylformamide / 0 - 20 °C

3.1: 80 percent / NaOiPr / propan-2-ol / Heating

With sodium isopropylate; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In water; N,N-dimethyl-formamide; isopropyl alcohol;
DOI:10.1016/S0223-5234(01)01251-X

Reference yield:

: 51-59-2
N-Acetyl-5-aminosalicylic acid

: 400039-29-4
5-acetylamino-N-butyl-2-(3-methyl-but-2-enyloxy)-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: 1-hydroxybenzotriazole; N,N'-dicyclohexylcarbodiimide / dimethylformamide / 0.5 h / 0 °C

1.2: 86 percent / dimethylformamide / 0 - 20 °C

2.1: 80 percent / NaOiPr / propan-2-ol / Heating

With sodium isopropylate; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide; isopropyl alcohol;
DOI:10.1016/S0223-5234(01)01251-X