Butanoic acid, 3-(benzoylamino)-, methyl ester

Base Information

Chemical Name:Butanoic acid, 3-(benzoylamino)-, methyl ester
CAS No.:112979-39-2
Molecular Formula:C12H15NO3
Molecular Weight:221.256
Hs Code.:
DSSTox Substance ID:DTXSID70446097
Nikkaji Number:J780.304D

Synonyms:112979-39-2;Butanoic acid, 3-(benzoylamino)-, methyl ester;SCHEMBL1185757;DTXSID70446097;AKOS008860212;3-(Benzoylamino)butyric acid methyl ester

Suppliers and Price of Butanoic acid, 3-(benzoylamino)-, methyl ester

Supply Marketing:

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

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Chemical Property of Butanoic acid, 3-(benzoylamino)-, methyl ester

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:221.10519334
Heavy Atom Count:16
Complexity:247

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(CC(=O)OC)NC(=O)C1=CC=CC=C1

Technology Process of Butanoic acid, 3-(benzoylamino)-, methyl ester

There total 8 articles about Butanoic acid, 3-(benzoylamino)-, methyl ester 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%

: 67-56-1
methanol

: 83509-86-8
N-benzoyl-3-aminobutyric acid

: 112979-39-2
methyl N-benzoyl-DL-β-homoalaninate

Guidance literature:: With chloro-trimethyl-silane;
DOI:10.1002/hlca.19880710724

Reference yield: 66.0%

: 77086-38-5
ketene t-butyldimethylsilyl methyl acetal

: 2198-64-3,1205-02-3,90988-29-7
N-Benzoylalanine

: 112979-39-2
methyl N-benzoyl-DL-β-homoalaninate

Guidance literature:: N-Benzoylalanine; With [bis(acetoxy)iodo]benzene; iodine; In dichloromethane;

ketene t-butyldimethylsilyl methyl acetal; With boron trifluoride diethyl etherate; In dichloromethane; at 20 ℃;
DOI:10.1021/jo9004487

Reference yield:

: 98-88-4
benzoyl chloride

: 112979-39-2
methyl N-benzoyl-DL-β-homoalaninate

Guidance literature:: Multi-step reaction with 2 steps

1: 21 g / NaOH / H₂O

2: 80 percent / Me₃SiCl

With sodium hydroxide; chloro-trimethyl-silane; In water;
DOI:10.1002/hlca.19880710724