Welcome to LookChem.com Sign In|Join Free
  • or
BOC-D-GLU(OFM)-OH is a versatile chemical compound and an amino acid derivative, characterized by the presence of a BOC (tert-butoxycarbonyl) protecting group on the amino group and an OFM (ortho-nitrofenylmethoxycarbonyl) protecting group on the carboxylic acid group. These protecting groups are strategically placed to allow for the compound's modification or incorporation into larger molecules under specific chemical conditions. It serves as a fundamental building block in organic synthesis, particularly in the realms of peptide synthesis and the development of drug molecules, as well as a valuable asset in organic chemistry research and development.

123417-20-9

Post Buying Request

123417-20-9 Suppliers

Recommended suppliers

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

123417-20-9 Usage

Uses

Used in Organic Synthesis:
BOC-D-GLU(OFM)-OH is used as a building block for the synthesis of various organic molecules, providing a foundation for the creation of complex structures and compounds.
Used in Peptide Synthesis:
In the field of peptide synthesis, BOC-D-GLU(OFM)-OH is utilized as a key component, enabling the formation of peptide bonds and contributing to the assembly of peptide sequences.
Used as a Precursor in Drug Development:
BOC-D-GLU(OFM)-OH is employed as a precursor for the development of various drug molecules, playing a crucial role in the design and synthesis of potential pharmaceuticals.
Used in Research and Development in Organic Chemistry:
BOC-D-GLU(OFM)-OH is also used in research and development within the field of organic chemistry, where it aids in the exploration of new reactions, mechanisms, and the synthesis of novel organic compounds.
Used in Pharmaceutical Industry:
BOC-D-GLU(OFM)-OH is used as a starting material for the synthesis of pharmaceuticals, facilitating the development of new drugs and therapeutic agents.
Used in Chemical Research:
In the chemical research industry, BOC-D-GLU(OFM)-OH is used as a reagent to study the properties and reactions of amino acid derivatives, contributing to the advancement of chemical knowledge and technology.

Check Digit Verification of cas no

The CAS Registry Mumber 123417-20-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,4,1 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 123417-20:
(8*1)+(7*2)+(6*3)+(5*4)+(4*1)+(3*7)+(2*2)+(1*0)=89
89 % 10 = 9
So 123417-20-9 is a valid CAS Registry Number.

123417-20-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name BOC-D-GLU(OFM)-OH

1.2 Other means of identification

Product number -
Other names BOC-D-GLUTAMIC ACID(OFM)-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:123417-20-9 SDS

123417-20-9Downstream Products

123417-20-9Relevant academic research and scientific papers

Solid-phase synthesis of peptidyl thioacids employing a 9-fluorenylmethyl thioester-based linker in conjunction with Boc chemistry

Crich, David,Sana, Kasinath

scheme or table, p. 7383 - 7388 (2010/01/16)

(Chemical Equation Presented) A method for the synthesis of peptidyl thioacids is described on the basis of the use of the N-[9-(thiomethyl)-9H- fluoren-2-yl]succinamic acid and cross-linked aminomethyl polystyrene resin. The method employs standard Boc chemistry SPPS techniques in conjunction with 9-fluorenylmethyloxycarbonyl protection of side-chain alcohols and amines and 9-fluorenylmethyl protection of side-chain acids and thiols. Cleavage from the resin is accomplished with piperidine, which also serves to remove the side-chain protection and avoids the HF conditions usually associated with the resin cleavage stage of Boc chemistry SPPS. The so-obtained thioacids are converted to simple thioesters in high yield by standard alkylation according to well-established methods. 2009 American Chemical Society.

Single step syntheses of ω-9-fluorenylmethyl esters of aspartic and glutamic acids

Belshaw,Adamson,Lajoie

, p. 1001 - 1005 (2007/10/02)

Base lability of the 9-fluorenylmethyl ester makes this group useful in solid phase peptide synthesis when used in combination with the tBoc methodology for preparing cyclic peptides. We describe a simple one step synthesis of the 9-fluorenylmethyl esters of aspartic and glutamic acids.

Convenient Syntheses of Fluorenylmethyl-Based Side Chain Derivatives of Glutamic and Aspartic acids, Lysine and Cysteine

Albericio, F.,Nicolas, E.,Rizo, J.,Ruiz-Gayo, M.,Pedroso, E.,Giralt, E.

, p. 119 - 122 (2007/10/02)

Efficient and practical one-pot syntheses of the fluorenylmethyl-based side chain derivatives of glutamic and aspartic acids, lysine, and cysteine are described.Likewise, stability/lability of these derivatives towards solvents and reagents used in solid

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 123417-20-9