2-[[4-(phenylazo)benzyl]sulphonyl]ethyl S-(acetamidomethyl)-N-[N-(tert-butoxycarbonyl)-L-seryl]-L-cysteinate

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Chemical plants supply high-quality 2-[[4-(phenylazo)benzyl]sulphonyl]ethyl S-(acetamidomethyl)-N-[N-(tert-butoxycarbonyl)-L-seryl]-L-cysteinate 76408-56-5 in bulk

  • Molecular Formula: C29H39 N5 O9 S2
  • Molecular Weight: 665.77806
  • Vapor Pressure: 0mmHg at 25°C 
  • Boiling Point: 967°C at 760 mmHg 
  • Flash Point: 538.6°C 
  • PSA: 246.07000 
  • Density: 1.32g/cm3 
  • LogP: 5.72300 

2-[[4-(phenylazo)benzyl]sulphonyl]ethyl S-(acetamidomethyl)-N-[N-(tert-butoxycarbonyl)-L-seryl]-L-cysteinate(Cas 76408-56-5) Usage

Sulphonyl group

A functional group consisting of a sulfur atom bonded to two oxygen atoms (-SO2), which can impart certain chemical reactivity and properties to the compound.

Benzyl group with azo linkage

A phenyl ring (a six-membered aromatic ring with a single bond between two carbon atoms) connected to a secondary amine group through a nitrogen-nitrogen double bond (-N=N-). This azo linkage can be responsible for the compound's color and may undergo redox reactions.

N-tert-butoxycarbonyl-L-seryl-L-cysteinate moiety

A part of the molecule that consists of an N-tert-butoxycarbonyl group (a protecting group for amines and alcohols), an L-seryl (an amino acid with a hydroxyl group), and an L-cysteinate (an amino acid with a thiol group). This moiety can provide specific biological activity and reactivity.

S-(acetamidomethyl) group

An acetylated aminomethyl group (-CH2-NH-COCH3) attached to the ethyl group. This group can protect the amino group from unwanted reactions and can be removed under specific conditions to reveal the free amino group.

Potential applications in pharmaceuticals or biotechnology

Due to its complex structure and various functional groups, 2-[[4-(phenylazo)benzyl]sulphonyl]ethyl S-(acetamidomethyl)-N-[N-(tert-butoxycarbonyl)-L-seryl]-L-cysteinate may have potential uses in drug delivery, enzyme inhibition, or as a precursor for the synthesis of other biologically active compounds.

Possible roles as a targeted delivery system or precursor

The presence of specific functional groups and amino acid moieties in the compound may allow it to be used as a targeted delivery system for drugs or other molecules, or as a precursor for the synthesis of other compounds with desired properties.

Need for further research and analysis

To determine the precise properties and potential uses of 2-[[4-(phenylazo)benzyl]sulphonyl]ethyl S-(acetamidomethyl)-N-[N-(tert-butoxycarbonyl)-L-seryl]-L-cysteinate, additional research and analysis in a laboratory setting would be required. This may include studying its solubility, stability, reactivity, and biological activity, as well as exploring its potential applications in drug development or biotechnology.

General Description

The chemical "2-[[4-(phenylazo)benzyl]sulphonyl]ethyl S-(acetamidomethyl)-N-[N-(tert-butoxycarbonyl)-L-seryl]-L-cysteinate" is a compound that contains a sulphonyl group, a benzyl group with an azo linkage, and an N-tert-butoxycarbonyl-L-seryl-L-cysteinate moiety. It also has an S-(acetamidomethyl) group attached to the ethyl group. This complex chemical structure indicates that it may have potential applications in pharmaceuticals or biotechnology, possibly as a targeted delivery system or as a precursor for the synthesis of other compounds. Its precise properties and potential uses would require further research and analysis in a laboratory setting.

InChI:InChI=1/C29H39N5O9S2/c1-20(36)30-19-44-17-25(31-26(37)24(16-35)32-28(39)43-29(2,3)4)27(38)42-14-15-45(40,41)18-21-10-12-23(13-11-21)34-33-22-8-6-5-7-9-22/h5-13,24-25,35H,14-19H2,1-4H3,(H,30,36)(H,31,37)(H,32,39)/t24-,25-/m0/s1

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