Catalog No.:AA00BZQK

3618-96-0 | Ac-phe-ome

Name: Name:Ac-phe-ome
Brand: AABLOCKS
SKU: AA00BZQK
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Technical Information
Properties
Upstream Synthesis Route
Literature
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Technical Information
Properties
Upstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA00BZQK

Chemical Name:

Ac-phe-ome

CAS Number:

3618-96-0

Molecular Formula:

C12H15NO3

Molecular Weight:

221.2524

MDL Number:

MFCD00066060

SMILES:

COC(=O)[C@H](Cc1ccccc1)NC(=O)C

Properties

BP:

391°C at 760 mmHg

Form:

Solid

Storage:

Keep in dry area;Room Temperature;

Computed Properties

Complexity:

247

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

0.9

Upstream Synthesis Route

3618-96-0

52485-51-5

[1]ChemicalCommunications,2015,vol.51,#49,p.9991-9994

[2]Tetrahedron,2014,vol.70,#31,p.4602-4610

Literature

Title: Photostability of amino acids: photodissociation dynamics of phenylalanine chromophores.

Journal: Physical chemistry chemical physics : PCCP 20100521

Title: Pseudopolymorphism of N-acetyl-L-phenylalanine methyl ester.

Journal: Acta crystallographica. Section B, Structural science 20080401

Title: Molecular recognition in cyclodextrin complexes of amino acid derivatives: the effects of kinetic energy on the molecular recognition of a pseudopeptide in a nonconstraining host environment as revealed by a temperature-dependent crystallographic study.

Journal: The journal of physical chemistry. B 20061228

Title: Molecular recognition in cyclodextrin complexes of amino acid derivatives. 1. Crystallographic studies of beta-cyclodextrin complexes with N-acetyl-L-phenylalanine methyl ester and N-acetyl-L-phenylalanine amide pseudopeptides.

Journal: Journal of the American Chemical Society 20011010

Title: Variations in the enantioselectivity of salt-activated subtilisin induced by lyophilization.

Journal: Biotechnology and bioengineering 20010505

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