Welcome to LookChem.com Sign In|Join Free
  • or
2-(Fmoc-amino)-4-pentynoic acid is a versatile chemical compound that features an amino group and a pentynoic acid group attached to a central aromatic ring. The Fmoc (9-fluorenylmethyloxycarbonyl) group acts as a protecting group for the amino group, enabling selective reactivity manipulation, while the pentynoic acid group confers a terminal alkyne functionality, making the compound suitable for click chemistry reactions and other synthetic transformations. 2-(Fmoc-amino)-4-pentynoic acid plays a significant role as a building block in peptide synthesis, contributing to its importance in chemical synthesis.

191215-87-9

Post Buying Request

191215-87-9 Suppliers

Recommended suppliers

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

191215-87-9 Usage

Uses

Used in Pharmaceutical Industry:
2-(Fmoc-amino)-4-pentynoic acid is used as a building block for peptide synthesis, facilitating the creation of complex peptide structures that are crucial for the development of new pharmaceuticals. Its protective Fmoc group allows for controlled synthesis, reducing side reactions and improving the yield of desired peptide products.
Used in Chemical Synthesis:
In the field of chemical synthesis, 2-(Fmoc-amino)-4-pentynoic acid is utilized as a versatile intermediate for the synthesis of various organic compounds. Its terminal alkyne functionality enables it to participate in click chemistry reactions, which are highly efficient and selective, allowing for the rapid assembly of complex molecules.
Used in Bioconjugation:
2-(Fmoc-amino)-4-pentynoic acid is used as a bioconjugation agent for the attachment of peptides or other biomolecules to various surfaces or materials. Its alkyne group can be selectively reacted with azide-containing compounds through click chemistry, enabling the formation of stable triazole linkages for immobilization or modification purposes.
Used in Materials Science:
In materials science, 2-(Fmoc-amino)-4-pentynoic acid is employed as a functional component in the development of novel materials with specific properties. Its ability to participate in click chemistry reactions allows for the precise and efficient incorporation of peptide sequences into polymers, gels, or other material structures, potentially enhancing their properties or imparting new functionalities.

Check Digit Verification of cas no

The CAS Registry Mumber 191215-87-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,1,2,1 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 191215-87:
(8*1)+(7*9)+(6*1)+(5*2)+(4*1)+(3*5)+(2*8)+(1*7)=129
129 % 10 = 9
So 191215-87-9 is a valid CAS Registry Number.

191215-87-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name L-N-Fmoc-propargylglycine

1.2 Other means of identification

Product number -
Other names 2-(9H-fluoren-9-ylmethoxycarbonylamino)-pent-4-ynoic acid

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:191215-87-9 SDS

191215-87-9Upstream product

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 191215-87-9