183249-68-5

Basic information

• Product Name: [3-(3-benzyloxycarbonylaminopropylamino)propyl]carbamic acid benzyl ester
• Synonyms: [3-(3-benzyloxycarbonylaminopropylamino)propyl]carbamic acid benzyl ester
• CAS NO: 183249-68-5
• Molecular Weight: 399.49
• Mol File: 183249-68-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: [3-(3-benzyloxycarbonylaminopropylamino)propyl]carbamic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [3-(3-benzyloxycarbonylaminopropylamino)propyl]carbamic acid benzyl ester(183249-68-5)
• EPA Substance Registry System: [3-(3-benzyloxycarbonylaminopropylamino)propyl]carbamic acid benzyl ester(183249-68-5)

Safety Data

• Hazardous Substances Data: 183249-68-5(Hazardous Substances Data)

Usage

Description

[3-(3-benzyloxycarbonylaminopropylamino)propyl]carbamic acid benzyl ester is a complex carbamic acid ester chemical compound, characterized by the presence of both a benzyloxy and a benzyl functional group. It is an amino acid derivative, featuring a propylamine moiety connected to the carbamic acid through a three-carbon linker. [3-(3-benzyloxycarbonylaminopropylamino)propyl]carbamic acid benzyl ester's intricate structure and potential reactivity make it a candidate for applications in organic synthesis and as a pharmaceutical intermediate.

Uses

Used in Organic Synthesis:
[3-(3-benzyloxycarbonylaminopropylamino)propyl]carbamic acid benzyl ester is used as a synthetic building block for the creation of more complex organic molecules. Its unique structure allows for various chemical reactions, making it a valuable component in the synthesis of novel compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [3-(3-benzyloxycarbonylaminopropylamino)propyl]carbamic acid benzyl ester is used as a potential intermediate in the development of new drugs. Its complex structure and functional groups may contribute to the design of innovative therapeutic agents, targeting specific biological pathways or receptors.
Used in Research and Development:
[3-(3-benzyloxycarbonylaminopropylamino)propyl]carbamic acid benzyl ester is also utilized in research and development settings, where its reactivity and structural features are studied to understand its potential applications and interactions with other molecules. This knowledge can be applied to the design of new drugs or materials with specific properties and functions.

Upstream product

• 56-18-8 bis(3-aminopropyl)amine 
• 5532-86-5 benzyl cyanoformate 
• 28170-07-2 benzyl phenyl carbonate 
• 530-62-1 1,1'-carbonyldiimidazole 
• 100-51-6 benzyl alcohol 
• 501-53-1 benzyl chloroformate 
• 22129-07-3 N-benzyloxycarbonylimidazole 

Downstream Products

• 199737-11-6 N,N-Bis-(3-benzyloxycarbonylamino-propyl)-succinamic acid 
• 1145787-28-5 C₂₈H₃₃N₅O₇ 
• 187411-84-3 (3-{(3-Benzyloxycarbonylamino-propyl)-[(6-{2-[bis-(3-benzyloxycarbonylamino-propyl)-amino]-acetylamino}-hexylcarbamoyl)-methyl]-amino}-propyl)-carbamic acid benzyl ester 
• 183249-77-6 [Bis-(3-{2-[bis-(3-benzyloxycarbonylamino-propyl)-amino]-acetylamino}-propyl)-amino]-acetic acid 
• 183249-76-5 [Bis-(3-{2-[bis-(3-benzyloxycarbonylamino-propyl)-amino]-acetylamino}-propyl)-amino]-acetic acid tert-butyl ester 
• 380848-83-9 bis(3-benzyloxycarbonylaminopropyl)-N-tert-butoxycarbonylamine 
• 183249-70-9 [Bis-(3-benzyloxycarbonylamino-propyl)-amino]-acetic acid tert-butyl ester 

Relevant articles and documents

pyrrole Shalom intermediates

The invention particularly relates to an amine phosphate binder bixalomer intermediate and a preparation method thereof. The preparation method comprises the following steps: reacting a raw material 3,3'-diamidodipropyl amine under the action of benzyl chloroformate to obtain 3,3'-dibenzyloxyamidodipropyl amine, carrying out substitution reaction on the 3,3'-dibenzyloxyamidodipropyl amine and 1,4-dibromobutane or 1,4-dichlorobutane to obtain N,N,N',N'-tetra(3-dibenzyloxyamido)-1,4-butanediamine, and carrying out deprotection by pressure hydrogenation under the action of Pd-C to obtain N,N,N',N'-tetra(3-aminopropyl)-1,4-butanediamine. The method has the advantages of cheap and accessible raw materials, operable reaction, high yield and fewer three wastes, and thus, has excellent industrial prospects.

Synthesis of peptide dendrimers based on a β-cyclodextrin core with guest binding ability

The synthesis of three first-order dendrimers based on a β-cyclodextrin core containing fourteen Val, Phe and Val-Phe residues is described. The guest binding ability of the tetradecavalent peptidyl β-cyclodextrin derivative has been tested by calorimetric titration and the thermodynamic parameters for the complex formation with adamantanecarboxylic acid were obtained.

Synthesis of new α-thiosialodendrimers and their binding properties to the sialic acid specific lectin from Limax flavus

Carbohydrate-protein binding interactions can be greatly amplified using the cluster or multivalent effect. In previous studies, sialylated multibranched L-lysine dendrimers were found to be potent inhibitors of the hemagglutination of human erythrocytes