Welcome to LookChem.com Sign In|Join Free

CAS

  • or

149303-38-8

Post Buying Request

149303-38-8 Suppliers

Recommended suppliersmore

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

149303-38-8 Usage

Chemical Properties

White powder

Uses

Fmoc-beta-Ala-OPfp is an Fmoc protected alanine derivative. Also, it is a reagent used in the synthesis of benzophenone-peptide nucleic acids derivative for mitochondrial targeting.

Check Digit Verification of cas no

The CAS Registry Mumber 149303-38-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,3,0 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 149303-38:
(8*1)+(7*4)+(6*9)+(5*3)+(4*0)+(3*3)+(2*3)+(1*8)=128
128 % 10 = 8
So 149303-38-8 is a valid CAS Registry Number.

149303-38-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name pentafluorophenyl 3-[[(9H-fluoren-9-yl)methyloxy]carbonylamino]propionate

1.2 Other means of identification

Product number -
Other names FMOC-B-ALA-OPFP

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:149303-38-8 SDS

149303-38-8Relevant articles and documents

Solution phase synthesis of β-peptides using micro reactors

Watts, Paul,Wiles, Charlotte,Haswell, Stephen J,Pombo-Villar, Esteban

, p. 5427 - 5439 (2007/10/03)

The synthesis of β-peptides has been successfully performed using a borosilicate glass micro reactor, in which a network of channels has been produced using a photolithographic and wet etching method. The reagents were mobilised by electroosmotic flow (EOF). The micro reactor was initially evaluated using a carbodiimide coupling reaction to form a dipeptide. The methodology has been extended such that the peptides may also be produced via the pentafluorophenyl ester derivatives of amino acids. It was found that performing the pentafluorophenyl ester reactions in the micro reactor resulted in an increase in the reaction efficiency over the traditional batch method. We postulate that the enhancement in rate of reaction is an electrochemical phenomenon, due to the reaction being performed in an electric field, which is unique to micro reactor systems. It has also been demonstrated that selective deprotection of the resultant dipeptides can be achieved. This approach has been used in the synthesis of a tripeptide.

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 149303-38-8