Welcome to LookChem.com Sign In|Join Free

CAS

  • or

67586-06-5

Post Buying Request

67586-06-5 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

67586-06-5 Usage

Description

(2S)-2-[(Benzyloxy)carbonyl](methyl)amino-3-[4-(tert-butoxy)phenyl]propanoic acid is a complex organic compound with a 2S configuration, featuring a benzyl carbonyl, methylamino, and tert-butoxy phenyl groups attached to a propanoic acid backbone. This intricate molecular structure likely endows it with unique properties and functions, making it a candidate for various applications in fields such as organic synthesis and pharmaceuticals.

Uses

Used in Organic Synthesis:
(2S)-2-[(Benzyloxy)carbonyl](methyl)amino-3-[4-(tert-butoxy)phenyl]propanoic acid is used as a building block in organic synthesis for its complex molecular structure and functional groups, which can be utilized to create a variety of new compounds with potential applications in different industries.
Used in Pharmaceutical Industry:
(2S)-2-[(Benzyloxy)carbonyl](methyl)amino-3-[4-(tert-butoxy)phenyl]propanoic acid is used as a potential pharmaceutical compound due to its unique molecular structure and functional groups. Further research and analysis would be required to fully understand its potential therapeutic applications and effects on human health.

Check Digit Verification of cas no

The CAS Registry Mumber 67586-06-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,8 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67586-06:
(7*6)+(6*7)+(5*5)+(4*8)+(3*6)+(2*0)+(1*6)=165
165 % 10 = 5
So 67586-06-5 is a valid CAS Registry Number.

67586-06-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Cbz-N-methyl-(O-tert-butyl)tyrosine

1.2 Other means of identification

Product number -
Other names Z-MeTyr(But)-OH

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:67586-06-5 SDS

67586-06-5Relevant articles and documents

Synthesis, conformational, properties, and antibody recognition of peptides containing β-turn mimetics based on α-alkylproline derivates

Hinds,Welsh,Brennand,Fisher,Glennie,Richards,Turner,Robinson

, p. 1777 - 1789 (2007/10/02)

Peptide recognition by monoclonal antibodies may provide a useful model for drug development, in particular to test the effects of conformational restriction on ligand binding. We have tested the influence of novel peptide mimetics upon conformation and binding affinity for the case of monoclonal antibodies raised to a peptide antigen which displays a preference for a β-turn conformation in aqueous solution. Two monoclonals were isolated that recognized the peptide Ac-Tyr-Pro-Tyr-Asp-Val-Pro-Asp-Tyr-Ala specifically at the β-turn formed by Tyr-Pro-Tyr-Asp. Peptide analogues were then synthesized containing mimetics designed to stabilize this conformation. One, analogue (3), contained a spirocyclic γ-lactam bridge between the α-position of proline-2 and the N atom of tyrosine-3, while another (2) contained (S)-α-methylproline at position 2. NMR spectroscopy and molecular modeling suggest that both analogues adopt reverse-turn conformations stablized relative to that in the native sequence. For the (S)-α-methylproline analogue binding to both monoclonal antibodies was substantially improved, compared with the native antigen, whereas the γ-lactam analogue (3) was not recognized by either antibody. Quantitative equilibrium ultrafiltration binding assays showed that the affinities of the (S)-α-methylproline analogue (2) for the two antibodies were improved over those measured with the native antigen by -2.3 and -0.65 kcal/mol. The origins of these free energy differences cannot be explained wholly on the basis of presumed extra hydrophobic contacts between the new methyl substituent and the antigen binding sites. We propose that the increased conformational stability of the analogue plays a decisive role, implying that the reverse turn detected in the native antigen, possibly a type-I turn, is important for recognition by the two antibodies.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 67586-06-5