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143824-77-5

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143824-77-5 Usage

Description

FMOC-ARG(BOC)2-OH, also known as Fmoc-Arginine(Boc)2, is a synthetic compound used in the field of organic chemistry and peptide synthesis. It is a white to off-white powder with specific chemical properties that make it a valuable intermediate in the synthesis of various peptides and proteins.

Uses

Used in Pharmaceutical Industry:
FMOC-ARG(BOC)2-OH is used as an intermediate in membrane-enhanced peptide synthesis for the development of new drugs and therapeutic agents. Its role in peptide synthesis is crucial, as it aids in the formation of complex peptide structures that can be used for various medical applications, including the treatment of diseases and the development of vaccines.
Used in Research and Development:
In the field of research and development, FMOC-ARG(BOC)2-OH is utilized for the synthesis of custom peptides and proteins. This allows scientists to study the structure, function, and interactions of these biomolecules, leading to a better understanding of their roles in biological processes and the potential for new therapeutic strategies.
Used in Chemical Synthesis:
FMOC-ARG(BOC)2-OH is also used in chemical synthesis for the production of various compounds with specific properties. Its versatility as a synthetic intermediate makes it a valuable tool in the development of new materials and chemicals for a wide range of applications, from pharmaceuticals to industrial products.

Check Digit Verification of cas no

The CAS Registry Mumber 143824-77-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,8,2 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 143824-77:
(8*1)+(7*4)+(6*3)+(5*8)+(4*2)+(3*4)+(2*7)+(1*7)=135
135 % 10 = 5
So 143824-77-5 is a valid CAS Registry Number.
InChI:InChI=1/C31H40N4O8/c1-30(2,3)42-28(39)34-26(35-29(40)43-31(4,5)6)32-17-11-16-24(25(36)37)33-27(38)41-18-23-21-14-9-7-12-19(21)20-13-8-10-15-22(20)23/h7-10,12-15,23-24H,11,16-18H2,1-6H3,(H,33,38)(H,36,37)(H2,32,34,35,39,40)/t24-/m0/s1

143824-77-5 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Detail
  • Alfa Aesar

  • (H63784)  Nomega,Nomega'-Di-Boc-Nalpha-Fmoc-L-arginine, 95%   

  • 143824-77-5

  • 250mg

  • 735.0CNY

  • Detail
  • Alfa Aesar

  • (H63784)  Nomega,Nomega'-Di-Boc-Nalpha-Fmoc-L-arginine, 95%   

  • 143824-77-5

  • 1g

  • 2205.0CNY

  • Detail
  • Alfa Aesar

  • (H63784)  Nomega,Nomega'-Di-Boc-Nalpha-Fmoc-L-arginine, 95%   

  • 143824-77-5

  • 5g

  • 8820.0CNY

  • Detail

143824-77-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name FMOC-ARG(BOC)2-OH

1.2 Other means of identification

Product number -
Other names FMOC-L-ARG(BOC)2-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:143824-77-5 SDS

143824-77-5Relevant articles and documents

Modular Solid-Phase Synthesis of Antiprotozoal Barnesin Derivatives

Roman, Dávid,Ragu?, Luka,Keiff, Fran?ois,Meyer, Florian,Barthels, Fabian,Schirmeister, Tanja,Kloss, Florian,Beemelmanns, Christine

supporting information, p. 3744 - 3748 (2020/04/02)

Here, we applied and optimized a solid support (SP)-based Horner-Wadsworth-Emmons reagent to prepare SP-bound vinylogous amino acids. Subsequent SP-based peptide synthesis, global deprotection, and chemical modifications yielded 14 lipodipeptides carrying

Miraziridine A: Natures blueprint towards protease class-spanning inhibitors

Schaschke, Norbert

, p. 855 - 857 (2007/10/03)

The natural product miraziridine A isolated from the marine sponge Theonella aff. mirabilis unifies within one molecule three structurally privileged elements: (i) (2R,3R)-aziridine-2,3-dicarboxylic acid, (ii) (3S,4S)-4-amino-3-hydroxy-6-methylheptanoic acid (statine), and (iii) (E)-(S)-4-amino-7-guanidino-hept-2-enoic acid (vinylogous arginine). The alignment of them realized in the tetrapetide allows for a simultaneous inhibition of the proteolytic activity of trypsin-like serine proteases, papain-like cysteine proteases, and pepsin-like aspartyl proteases. Therefore, this unique compound represents a blueprint for the design of protease class-spanning inhibitors.

A facile preparation of Fmoc-Argω,ω′(Boc)2 -OH and Z-Argω,ω′ (Boc)2 -OH, new arginine derivatives for peptide synthesis

Verdini, Antonio S.,Lucietto, Pierluigi,Fossati, Gianluca,Giordani, Cristiana

, p. 6541 - 6542 (2007/10/02)

The new arginine derivatives Fmoc-Argω,ω′(Boc)2 -OH and Z-Argω,ω′ (Boc)2 -OH have been easily prepared in hiqh yield starting from Z-Orn-OH and N,N′-bis (tert-butoxycarbonyl) -S-methylisothiourea.

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