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ChemicalBook--->CAS DataBase List--->1244040-64-9

1244040-64-9

1244040-64-9 Structure

1244040-64-9 Structure
IdentificationBack Directory
[Name]

Bz-Tz-NHS
[CAS]

1244040-64-9
[Synonyms]

Tz-NHS
Bz-Tz-NHS
Benzylaminotetrazine-NHS
Tetrazine-Ph-NHCO-C3-NHS ester
Tetrazine-Ph-NHCO-C3-NHS ester,Bz-Tz-NHS
Benzylamino tetrazine N-hydroxysuccinimidyl ester
5-(4-(1,2,4,5-tetrazin-3-yl)benzylamino)-5-oxopentanoic acid succinimidyl ester
2,5-Dioxo-1-pyrrolidinyl 5-[4-(1,2,4,5-tetrazin-3-yl)benzylamino]-5-oxopentanoate
2,5-dioxopyrrolidin-1-yl 5-((4-(1,2,4,5-tetrazin-3-yl)benzyl)amino)-5-oxopentanoate
2,5-Dioxo-1-pyrrolidinyl 5-[4-(1,2,4,5-tetrazin-3-yl)benzylamino]-5-oxopentanoate >=90%
5-Oxo-5-[[[4-(1,2,4,5-tetrazin-3-yl)phenyl]methyl]amino]pentanoic acid 2,5-dioxo-1-pyrrolidinyl ester
Pentanoic acid, 5-oxo-5-[[[4-(1,2,4,5-tetrazin-3-yl)phenyl]methyl]amino]-, 2,5-dioxo-1-pyrrolidinyl ester
Tetrazine Ph NHCO C3 NHS ester,Inhibitor,inhibit,Tetrazine-Ph-NHCO-C-3-NHS ester,TetrazinePhNHCOC3NHS ester,PROTAC Linkers
5-Oxo-5-[[[4-(1,2,4,5-tetrazin-3-yl)phenyl]methyl]amino]pentanoic acid 2,5-dioxo-1-pyrrolidinyl ester, Benzylamino tetrazine N-hydroxysuccinimidyl ester, Benzylaminotetrazine-NHS, Bz-Tz-NHS
[Molecular Formula]

C18H18N6O5
[MDL Number]

MFCD32067811
[MOL File]

1244040-64-9.mol
[Molecular Weight]

398.373
Chemical PropertiesBack Directory
[density ]

1.45±0.1 g/cm3(Predicted)
[storage temp. ]

-20°C
[solubility ]

DMSO : 100 mg/mL (251.02 mM; Need ultrasonic)
[form ]

Solid
[pka]

14.57±0.46(Predicted)
[color ]

Pink to red
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

Succinimidyl ester functionalized tetrazine for inverse electron demand Diels-Alder cycloaddition reactions. Succinimidyl ester will react with amines for small molecule, biomolecule or surface modification. Tetrazine will react with strained alkenes such as transcyclooctene, norbornene and cyclopropene to yield a stable covalent linkage. Tetrazines have proven useful in bioorthogonal reactions for many biological imaging and bioconjugation applications.
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