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214750-77-3

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214750-77-3 Usage

Description

BOC-D-PHE(4-NHBOC)-OH, also known as Fmoc-4-(Boc-amino)-D-phenylalanine, is a chemical compound that serves as an intermediate in the synthesis of various pharmaceuticals and bioactive molecules. It is a white powder with specific chemical properties that make it a valuable component in the development of targeted therapies and inhibitors.

Uses

Used in Pharmaceutical Synthesis:
BOC-D-PHE(4-NHBOC)-OH is used as an intermediate for the preparation of doxorubicin-formaldehyde peptide conjugates, which target αvβ3 integrin. This application is crucial in the development of targeted therapies for various diseases, including cancer.
Used in Caspases Inhibition:
BOC-D-PHE(4-NHBOC)-OH is also utilized in the synthesis of peptide acyloxymethyl ketones, which act as selective caspases inhibitors. These inhibitors play a significant role in regulating cellular processes and have potential applications in the treatment of various conditions, such as neurodegenerative diseases and cancer.
Used in the Chemical Industry:
In the chemical industry, BOC-D-PHE(4-NHBOC)-OH may be used as a building block for the synthesis of more complex molecules with specific functions and properties. Its versatility as an intermediate allows for the creation of a wide range of products with potential applications in various fields.
Used in Research and Development:
BOC-D-PHE(4-NHBOC)-OH is an essential compound in the field of research and development, where it is employed to study the structure-activity relationships of various bioactive molecules. This knowledge can lead to the discovery of new therapeutic agents and a better understanding of molecular interactions.

Check Digit Verification of cas no

The CAS Registry Mumber 214750-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,7,5 and 0 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 214750-77:
(8*2)+(7*1)+(6*4)+(5*7)+(4*5)+(3*0)+(2*7)+(1*7)=123
123 % 10 = 3
So 214750-77-3 is a valid CAS Registry Number.
InChI:InChI=1/C29H30N2O6/c1-29(2,3)37-28(35)30-19-14-12-18(13-15-19)16-25(26(32)33)31-27(34)36-17-24-22-10-6-4-8-20(22)21-9-5-7-11-23(21)24/h4-15,24-25H,16-17H2,1-3H3,(H,30,35)(H,31,34)(H,32,33)/t25-/m1/s1

214750-77-3 Well-known Company Product Price

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  • Alfa Aesar

  • (H66616)  4-(Boc-amino)-N-Fmoc-D-phenylalanine, 95%   

  • 214750-77-3

  • 250mg

  • 294.0CNY

  • Detail
  • Alfa Aesar

  • (H66616)  4-(Boc-amino)-N-Fmoc-D-phenylalanine, 95%   

  • 214750-77-3

  • 1g

  • 784.0CNY

  • Detail
  • Alfa Aesar

  • (H66616)  4-(Boc-amino)-N-Fmoc-D-phenylalanine, 95%   

  • 214750-77-3

  • 5g

  • 2940.0CNY

  • Detail

214750-77-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[4-[(2-methylpropan-2-yl)oxycarbonylamino]phenyl]propanoic acid

1.2 Other means of identification

Product number -
Other names 4-(Boc-amino)-N-Fmoc-D-phenylalanine

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:214750-77-3 SDS

214750-77-3Relevant articles and documents

Incorporation of non-natural amino acids improves cell permeability and potency of specific inhibitors of proteasome trypsin-like sites

Geurink, Paul P.,Van Der Linden, Wouter A.,Mirabella, Anne C.,Gallastegui, Nerea,De Bruin, Gerjan,Blom, Annet E. M.,Voges, Mathias J.,Mock, Elliot D.,Florea, Bogdan I.,Van Der Marel, Gijs A.,Driessen, Christoph,Van Der Stelt, Mario,Groll, Michael,Overkleeft, Herman S.,Kisselev, Alexei F.

supporting information, p. 1262 - 1275 (2013/03/29)

Proteasomes degrade the majority of proteins in mammalian cells by a concerted action of three distinct pairs of active sites. The chymotrypsin-like sites are targets of antimyeloma agents bortezomib and carfilzomib. Inhibitors of the trypsin-like site se

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