Welcome to LookChem.com Sign In|Join Free

CAS

  • or

30802-26-7

Post Buying Request

30802-26-7 Suppliers

Recommended suppliersmore

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

30802-26-7 Usage

General Description

AC-ALA-ALA-OME is a synthetic compound that contains the amino acid alanine linked to the fatty acid omega-methoxyethyl. It is often used in the field of drug design and chemical biology as a building block for the synthesis of peptides and peptidomimetics. AC-ALA-ALA-OME may have potential therapeutic applications due to its ability to target specific receptors or enzymes in the body. Additionally, AC-ALA-ALA-OME could also be utilized as a research tool for studying protein-protein interactions and developing new drug candidates with improved pharmacokinetic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 30802-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,8,0 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 30802-26:
(7*3)+(6*0)+(5*8)+(4*0)+(3*2)+(2*2)+(1*6)=77
77 % 10 = 7
So 30802-26-7 is a valid CAS Registry Number.

30802-26-7SDS

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 Ac-Ala-Ala-OMe

1.2 Other means of identification

Product number -
Other names N-acetyl-L-alanyl-L-alanine methyl 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:30802-26-7 SDS

30802-26-7Relevant articles and documents

COMPOUNDS FOR AMIDE-FORMING REACTIONS

-

Page/Page column 11; 18, (2014/01/07)

Provided herein is a compound of Formula I, that displays remarkable physicochemical properties as a peptide-coupling additive for peptide-forming reactions in water, wherein said coupling reactions proceed without measurable racemization. A method of pro

Thermitase - A Thermostable Serine Protease. I. Synthesis of Alanine Peptide Esters as Substrates of the Enzyme

Jahreis, Guenther,Fittkau, Siegfried

, p. 35 - 40 (2007/10/02)

The synthesis of N-acetylated and N-succinylated peptide esters of alanine is described.The peptides are built up from the Z-protected peptides by liquid phase fragment condensation and by acylation of the deprotected peptide esters.The kinetic parameters Km and kcat of some compounds are presented.

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 30802-26-7