Welcome to LookChem.com Sign In|Join Free
  • or
BOC-SER(FMOC-GLY)-OH is a chemical compound consisting of three amino acid residues: BOC-SER, FMOC-GLY, and OH. It features a serine amino acid with a tert-butyloxycarbonyl (BOC) protecting group, a glycine amino acid with a 9-fluorenylmethyloxycarbonyl (FMOC) protecting group, and a carboxylic acid group. BOC-SER(FMOC-GLY)-OH is widely utilized in peptide synthesis, where the protecting groups can be removed to generate free amine and carboxylic acid groups for subsequent chemical reactions. Its versatility and functionality make it a valuable component in the production of peptides and other biological molecules in laboratory settings.

944283-06-1

Post Buying Request

944283-06-1 Suppliers

Recommended suppliers

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

944283-06-1 Usage

Uses

Used in Pharmaceutical Industry:
BOC-SER(FMOC-GLY)-OH is used as a building block for the synthesis of peptides and other bioactive molecules for various therapeutic applications. Its protecting groups ensure the correct sequence and structure of the peptide during synthesis, which is crucial for the biological activity and efficacy of the final product.
Used in Research and Development:
In the field of research and development, BOC-SER(FMOC-GLY)-OH serves as a key component in the design and synthesis of novel peptides with potential applications in drug discovery, diagnostics, and therapeutics. Its versatility allows researchers to explore new peptide sequences and structures with specific biological functions.
Used in Diagnostics:
BOC-SER(FMOC-GLY)-OH is employed in the development of diagnostic tools, such as immunoassays and biosensors, where specific peptide sequences are required for the detection and quantification of target molecules. Its ability to form stable and functional peptides makes it an essential component in these diagnostic applications.
Used in Cosmetics Industry:
In the cosmetics industry, BOC-SER(FMOC-GLY)-OH is used as a component in the synthesis of bioactive peptides for skincare products. These peptides can have various functions, such as promoting collagen production, reducing inflammation, or protecting the skin from environmental stressors, thereby contributing to the overall effectiveness of cosmetic formulations.
Used in Agricultural Industry:
BOC-SER(FMOC-GLY)-OH can be utilized in the development of biopesticides and plant growth regulators, where specific peptide sequences can target pests or modulate plant growth and development. Its role in creating these bioactive molecules can contribute to more sustainable and environmentally friendly agricultural practices.

Check Digit Verification of cas no

The CAS Registry Mumber 944283-06-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,4,2,8 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 944283-06:
(8*9)+(7*4)+(6*4)+(5*2)+(4*8)+(3*3)+(2*0)+(1*6)=181
181 % 10 = 1
So 944283-06-1 is a valid CAS Registry Number.

944283-06-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name L-Serine, N-[(1,1-dimethylethoxy)carbonyl]-O-[N-[(9H-fluoren-9-ylmethoxy)carbonyl]glycyl]-

1.2 Other means of identification

Product number -
Other names BOC-SER(GLY-FMOC)-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:944283-06-1 SDS

944283-06-1Downstream Products

944283-06-1Relevant academic research and scientific papers

"o-Acyl isopeptide method" for peptide synthesis: Synthesis of forty kinds of "o-acyl isodipeptide unit" Boc-Ser/Thr(Fmoc-Xaa)-OH

Yoshiya, Taku,Taniguchi, Atsuhiko,Sohma, Youhei,Fukao, Fukue,Nakamura, Setsuko,Abe, Naoko,Ito, Nui,Skwarczynski, Mariusz,Kimura, Tooru,Hayashi, Yoshio,Kiso, Yoshiaki

, p. 1720 - 1730 (2007)

The O-acyl isopeptide method has recently received attention as an efficient synthetic method for peptides. Herein, forty kinds of "O-acyl isodipeptide unit" Boc-Ser/Thr(Fmoc-Xaa)-OH (1-40) were effectively synthesized in two-steps without epimerization. The O-acyl isodipeptide units are important building blocks to enable the routine use of the O-acyl isopeptide method. This journal is The Royal Society of Chemistry.

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 944283-06-1