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