2824-57-9,MFCD00022759
Catalog No.:AA00I589

2824-57-9 | Ac-Trp-OMe

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$19.00   $14.00
- +
5g
98%
in stock  
$37.00   $26.00
- +
25g
98%
in stock  
$94.00   $66.00
- +
100g
98%
in stock  
$295.00 $206.00
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00I589
Chemical Name:
Ac-Trp-OMe
CAS Number:
2824-57-9
Molecular Formula:
C14H16N2O3
Molecular Weight:
260.2884
MDL Number:
MFCD00022759
SMILES:
COC(=O)[C@H](Cc1c[nH]c2c1cccc2)NC(=O)C
Properties
Properties
 
BP:
512.1°C at 760 mmHg  
Form:
Solid  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
346  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
19  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
5  
XLogP3:
1.4  

Literature

Title: Ultrafast dynamics of nonequilibrium electron transfer in photoinduced redox cycle: solvent mediation and conformation flexibility.

Journal: The journal of physical chemistry. B 20120802

Title: Antioxidant activity of unexplored indole derivatives: synthesis and screening.

Journal: European journal of medicinal chemistry 20101101

Title: Cellular effects of peptide and protein hydroperoxides.

Journal: Free radical biology & medicine 20100415

Title: Oxidation and inactivation of SERCA by selective reaction of cysteine residues with amino acid peroxides.

Journal: Chemical research in toxicology 20071001

Title: Enhanced ligand affinity for receptors in which components of the binding site are independently mobile.

Journal: Chemistry & biology 20050101

Title: Infrared-induced conformational isomerization and vibrational relaxation dynamics in melatonin and 5-methoxy-N-acetyl tryptophan methyl amide.

Journal: The Journal of chemical physics 20040515

Title: A mass spectrometric and molecular orbital study of H2O loss from protonated tryptophan and oxidized tryptophan derivatives.

Journal: Rapid communications in mass spectrometry : RCM 20040101

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SDS
Tags:2824-57-9 Molecular Formula|2824-57-9 MDL|2824-57-9 SMILES|2824-57-9 Ac-Trp-OMe
Catalog No.: AA00I589
2824-57-9,MFCD00022759
2824-57-9 | Ac-Trp-OMe
Pack Size: 1g
Purity: 98%
in stock
$19.00 $14.00
Pack Size: 5g
Purity: 98%
in stock
$37.00 $26.00
Pack Size: 25g
Purity: 98%
in stock
$94.00 $66.00
Pack Size: 100g
Purity: 98%
in stock
$295.00 $206.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00I589
Chemical Name: Ac-Trp-OMe
CAS Number: 2824-57-9
Molecular Formula: C14H16N2O3
Molecular Weight: 260.2884
MDL Number: MFCD00022759
SMILES: COC(=O)[C@H](Cc1c[nH]c2c1cccc2)NC(=O)C
Properties
BP: 512.1°C at 760 mmHg  
Form: Solid  
Storage: Keep in dry area;2-8℃;  
Complexity: 346  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 19  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 5  
XLogP3: 1.4  
Literature fold

Title: Ultrafast dynamics of nonequilibrium electron transfer in photoinduced redox cycle: solvent mediation and conformation flexibility.

Journal: The journal of physical chemistry. B20120802

Title: Antioxidant activity of unexplored indole derivatives: synthesis and screening.

Journal: European journal of medicinal chemistry20101101

Title: Cellular effects of peptide and protein hydroperoxides.

Journal: Free radical biology & medicine20100415

Title: Oxidation and inactivation of SERCA by selective reaction of cysteine residues with amino acid peroxides.

Journal: Chemical research in toxicology20071001

Title: Enhanced ligand affinity for receptors in which components of the binding site are independently mobile.

Journal: Chemistry & biology20050101

Title: Infrared-induced conformational isomerization and vibrational relaxation dynamics in melatonin and 5-methoxy-N-acetyl tryptophan methyl amide.

Journal: The Journal of chemical physics20040515

Title: A mass spectrometric and molecular orbital study of H2O loss from protonated tryptophan and oxidized tryptophan derivatives.

Journal: Rapid communications in mass spectrometry : RCM20040101

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