555-48-6,MFCD06662103
Catalog No.:AA00DKHO

555-48-6 | 2-Amino-N-phenylacetamide

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$250.00   $175.00
- +
5g
98%
in stock  
$726.00 $508.00
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00DKHO
Chemical Name:
2-Amino-N-phenylacetamide
CAS Number:
555-48-6
Molecular Formula:
C8H10N2O
Molecular Weight:
150.1778
MDL Number:
MFCD06662103
SMILES:
NCC(=O)Nc1ccccc1
NSC Number:
226561
Properties
Computed Properties
 
Complexity:
130  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
0.2  

Literature

Title: A network-based multi-target computational estimation scheme for anticoagulant activities of compounds.

Journal: PloS one 20110101

Title: Heterologous expression of leader-less pga gene in Pichia pastoris: intracellular production of prokaryotic enzyme.

Journal: BMC biotechnology 20100101

Title: Protein engineering of penicillin acylase.

Journal: Acta naturae 20100101

Title: Synthesis of optically active amino acid derivatives via dynamic kinetic resolution.

Journal: The Journal of organic chemistry 20091218

Title: Mutation of Residue βF71 of Escherichia coli Penicillin Acylase Results in Enhanced Enantioselectivity and Improved Catalytic Properties.

Journal: Acta naturae 20091001

Title: Investigation of the terminal P4 domain in a series of D-phenylglycinamide-based factor Xa inhibitors.

Journal: Bioorganic & medicinal chemistry letters 20071215

Title: Increasing synthetic performance of penicillin G acylase from Bacillus megaterium by site-directed mutagenesis.

Journal: Applied microbiology and biotechnology 20070401

Title: Solid state NMR analysis of the dipolar couplings within and between distant CF3-groups in a membrane-bound peptide.

Journal: Journal of magnetic resonance (San Diego, Calif. : 1997) 20061101

Title: Microbial transformation of aniline derivatives: regioselective biotransformation and detoxification of 2-phenylenediamine by Bacillus cereus strain PDa-1.

Journal: Journal of bioscience and bioengineering 20060701

Title: Allosteric control of an ionotropic glutamate receptor with an optical switch.

Journal: Nature chemical biology 20060101

Title: Design of selective phenylglycine amide tissue factor/factor VIIa inhibitors.

Journal: Bioorganic & medicinal chemistry letters 20050201

Title: Highly diastereoselective heterogeneously catalyzed hydrogenation of enamines for the synthesis of chiral beta-amino acid derivatives.

Journal: Journal of the American Chemical Society 20040317

Title: Evaluation of magnetic polymer micro-beads as carriers of immobilised biocatalysts for selective and stereoselective transformations.

Journal: Biotechnology letters 20040201

Title: A four component coupling strategy for the synthesis of D-phenylglycinamide-derived non-covalent factor Xa inhibitors.

Journal: Bioorganic & medicinal chemistry letters 20030721

Title: Conjugation of penicillin acylase with the reactive copolymer of N-isopropylacrylamide: a step toward a thermosensitive industrial biocatalyst.

Journal: Biotechnology progress 20030101

Title: Enzyme distribution derived from macroscopic particle behavior of an industrial immobilized penicillin-G acylase.

Journal: Biotechnology progress 20030101

Title: Modelling of the enzymatic kinetically controlled synthesis of cephalexin: influence of diffusion limitation.

Journal: Biotechnology and bioengineering 20021105

Title: A two-step, one-pot enzymatic synthesis of cephalexin from D-phenylglycine nitrile.

Journal: Biotechnology and bioengineering 20020805

Title: Penicillin acylase-catalyzed ampicillin synthesis using a pH gradient: a new approach to optimization.

Journal: Biotechnology and bioengineering 20020605

Title: Evaluation of the performance of immobilized penicillin G acylase using active-site titration.

Journal: Biotechnology and bioengineering 20020520

Title: The role of hydrophobic active-site residues in substrate specificity and acyl transfer activity of penicillin acylase.

Journal: European journal of biochemistry 20020401

Title: Diastereoselective addition of allylzinc bromide to imines derived from (R)-phenylglycine amide.

Journal: Organic letters 20011129

Title: Modeling of the enzymatic kinetic synthesis of cephalexin--influence of substrate concentration and temperature.

Journal: Biotechnology and bioengineering 20010505

Title: Asymmetric strecker synthesis of alpha-amino acids via a crystallization-induced asymmetric transformation using (R)-phenylglycine amide as chiral auxiliary.

Journal: Organic letters 20010419

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Tags:555-48-6 Molecular Formula|555-48-6 MDL|555-48-6 SMILES|555-48-6 2-Amino-N-phenylacetamide
Catalog No.: AA00DKHO
555-48-6,MFCD06662103
555-48-6 | 2-Amino-N-phenylacetamide
Pack Size: 1g
Purity: 98%
in stock
$250.00 $175.00
Pack Size: 5g
Purity: 98%
in stock
$726.00 $508.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00DKHO
Chemical Name: 2-Amino-N-phenylacetamide
CAS Number: 555-48-6
Molecular Formula: C8H10N2O
Molecular Weight: 150.1778
MDL Number: MFCD06662103
SMILES: NCC(=O)Nc1ccccc1
NSC Number: 226561
Properties
Complexity: 130  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 0.2  
Literature fold

Title: A network-based multi-target computational estimation scheme for anticoagulant activities of compounds.

Journal: PloS one20110101

Title: Heterologous expression of leader-less pga gene in Pichia pastoris: intracellular production of prokaryotic enzyme.

Journal: BMC biotechnology20100101

Title: Protein engineering of penicillin acylase.

Journal: Acta naturae20100101

Title: Synthesis of optically active amino acid derivatives via dynamic kinetic resolution.

Journal: The Journal of organic chemistry20091218

Title: Mutation of Residue βF71 of Escherichia coli Penicillin Acylase Results in Enhanced Enantioselectivity and Improved Catalytic Properties.

Journal: Acta naturae20091001

Title: Investigation of the terminal P4 domain in a series of D-phenylglycinamide-based factor Xa inhibitors.

Journal: Bioorganic & medicinal chemistry letters20071215

Title: Increasing synthetic performance of penicillin G acylase from Bacillus megaterium by site-directed mutagenesis.

Journal: Applied microbiology and biotechnology20070401

Title: Solid state NMR analysis of the dipolar couplings within and between distant CF3-groups in a membrane-bound peptide.

Journal: Journal of magnetic resonance (San Diego, Calif. : 1997)20061101

Title: Microbial transformation of aniline derivatives: regioselective biotransformation and detoxification of 2-phenylenediamine by Bacillus cereus strain PDa-1.

Journal: Journal of bioscience and bioengineering20060701

Title: Allosteric control of an ionotropic glutamate receptor with an optical switch.

Journal: Nature chemical biology20060101

Title: Design of selective phenylglycine amide tissue factor/factor VIIa inhibitors.

Journal: Bioorganic & medicinal chemistry letters20050201

Title: Highly diastereoselective heterogeneously catalyzed hydrogenation of enamines for the synthesis of chiral beta-amino acid derivatives.

Journal: Journal of the American Chemical Society20040317

Title: Evaluation of magnetic polymer micro-beads as carriers of immobilised biocatalysts for selective and stereoselective transformations.

Journal: Biotechnology letters20040201

Title: A four component coupling strategy for the synthesis of D-phenylglycinamide-derived non-covalent factor Xa inhibitors.

Journal: Bioorganic & medicinal chemistry letters20030721

Title: Conjugation of penicillin acylase with the reactive copolymer of N-isopropylacrylamide: a step toward a thermosensitive industrial biocatalyst.

Journal: Biotechnology progress20030101

Title: Enzyme distribution derived from macroscopic particle behavior of an industrial immobilized penicillin-G acylase.

Journal: Biotechnology progress20030101

Title: Modelling of the enzymatic kinetically controlled synthesis of cephalexin: influence of diffusion limitation.

Journal: Biotechnology and bioengineering20021105

Title: A two-step, one-pot enzymatic synthesis of cephalexin from D-phenylglycine nitrile.

Journal: Biotechnology and bioengineering20020805

Title: Penicillin acylase-catalyzed ampicillin synthesis using a pH gradient: a new approach to optimization.

Journal: Biotechnology and bioengineering20020605

Title: Evaluation of the performance of immobilized penicillin G acylase using active-site titration.

Journal: Biotechnology and bioengineering20020520

Title: The role of hydrophobic active-site residues in substrate specificity and acyl transfer activity of penicillin acylase.

Journal: European journal of biochemistry20020401

Title: Diastereoselective addition of allylzinc bromide to imines derived from (R)-phenylglycine amide.

Journal: Organic letters20011129

Title: Modeling of the enzymatic kinetic synthesis of cephalexin--influence of substrate concentration and temperature.

Journal: Biotechnology and bioengineering20010505

Title: Asymmetric strecker synthesis of alpha-amino acids via a crystallization-induced asymmetric transformation using (R)-phenylglycine amide as chiral auxiliary.

Journal: Organic letters20010419

Building Blocks More >
52498-02-9
52498-02-9
3-(4-Methoxyphenyl)cyclobutan-1-one
AA00DKMW | MFCD11848455
4997-55-1
4997-55-1
3-ethyl-4-hydroxybenzonitrile
AA00DKYH | MFCD16997588
50916-56-8
50916-56-8
3-(2-aminoacetyl)benzonitrile hydrochloride
AA00DL99 | MFCD11847053
55456-55-8
55456-55-8
N,N'-desoxycarbadox
AA00DLL9 | MFCD01722570
474432-66-1
474432-66-1
FAUC-365
AA00DLWR | MFCD28160534
4327-52-0
4327-52-0
3-((2-Aminophenyl)thio)propanenitrile
AA00DN1H | MFCD00047835
55824-11-8
55824-11-8
Cannabigerovarol
AA00DP8Y | MFCD20275216
54370-01-3
54370-01-3
1-Bromo-2-(chloromethyl)-4,5-dimethoxybenzene
AA00DQQD | MFCD06655708
54969-37-8
54969-37-8
1-(1,4-Dimethylpiperazin-2-yl)ethanone
AA00DT55 | MFCD18971733
477319-09-8
477319-09-8
3-((3,4-Dimethylphenyl)amino)-1-(4-fluorophenyl)propan-1-one
AA00DV81 | MFCD03934011
Submit
© 2017 AA BLOCKS, INC. All rights reserved.