Welcome to LookChem.com Sign In|Join Free
  • or
"Benzyl N-[(benzyloxy)carbonyl]alanylphenylalaninate" is a complex organic compound with the chemical formula C34H33N1O6. It is a derivative of dipeptides, which are short chains of two amino acids linked by a peptide bond. In benzyl N-[(benzyloxy)carbonyl]alanylphenylalaninate, the two amino acids are alanine and phenylalanine. The alanine is modified with a benzyloxycarbonyl (Z) protecting group, which is commonly used in peptide synthesis to prevent unwanted side reactions. The phenylalanine is also part of the peptide chain. benzyl N-[(benzyloxy)carbonyl]alanylphenylalaninate is often used in the field of pharmaceuticals and biochemistry for the synthesis of larger peptide structures, taking advantage of the stability provided by the protecting groups during the synthesis process. The benzyl group can be later removed under certain conditions to yield the desired peptide sequence.

2543-29-5

Post Buying Request

2543-29-5 Suppliers

Recommended suppliers

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

2543-29-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2543-29-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,4 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2543-29:
(6*2)+(5*5)+(4*4)+(3*3)+(2*2)+(1*9)=75
75 % 10 = 5
So 2543-29-5 is a valid CAS Registry Number.

2543-29-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name benzyl 3-phenyl-2-[2-(phenylmethoxycarbonylamino)propanoylamino]propanoate

1.2 Other means of identification

Product number -
Other names N-benzyloxycarbonyl-L-alanyl-L-phenylalanine benzyl ester

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:2543-29-5 SDS

2543-29-5Relevant academic research and scientific papers

Small peptides as modular catalysts for the direct asymmetric aldol reaction: Ancient peptides with aldolase enzyme activity

Zou, Weibiao,Ibrahem, Ismail,Dziedzic, Pawel,Sunden, Henrik,Cordova, Armando

, p. 4946 - 4948 (2007/10/03)

Simple peptides and their analogues having a primary amino group as the catalytic residue mediate the direct asymmetric intermolecular aldol reaction with high stereoselectivity and furnish the corresponding aldol products with up to 99% ee; this intrinsic ability of highly modular peptides may explain the initial molecular evolution of aldolase enzymes. The Royal Society of Chemistry 2005.

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 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 2543-29-5