ChemicalBook--->CAS DataBase List--->1426827-79-3

1426827-79-3

1426827-79-3 Structure

1426827-79-3 Structure
IdentificationBack Directory
[Name]

BCN-Osu
[CAS]

1426827-79-3
[Synonyms]

BCN-Osu
BCN-CO-NHS
BCN NH ester
endo-BCN-NHS ester
endo-BCN-NHS carbonate
Click-easy? BCN N-hydroxysuccinimide ester I
(1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-ylmethyl Succinimidyl Carbonate
(1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-ylmethyl Succinimidyl Carbonate (2mg*5)
[(1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-yl]methyl (2,5-Dioxopyrrolidin-1-yl) Carbonate
rel-(1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-ylmethyl (2,5-dioxopyrrolidin-1-yl) carbonate
(1R,8S,9S)-BICYCLO[6.1.0]NON-4-YN-9-YLMETHYL?SUCCINIMIDYL?CARBONATE/BCN-Osu MFCD19705416
Carbonic acid, (1α,8α,9β)-bicyclo[6.1.0]non-4-yn-9-ylmethyl 2,5-dioxo-1-pyrrolidinyl ester
[Molecular Formula]

C15H17NO5
[MDL Number]

MFCD19705416
[MOL File]

1426827-79-3.mol
[Molecular Weight]

291.3
Chemical PropertiesBack Directory
[Melting point ]

120 °C
[Boiling point ]

412.8±28.0 °C(Predicted)
[density ]

1.35±0.1 g/cm3(Predicted)
[storage temp. ]

-20°C
[solubility ]

water: insoluble
[form ]

powder
[color ]

White to light yellow
[InChI]

InChI=1/C15H17NO5/c17-13-7-8-14(18)16(13)21-15(19)20-9-12-10-5-3-1-2-4-6-11(10)12/h10-12H,3-9H2/t10-,11+,12-
[InChIKey]

SKTDJYHCSCYLQU-ZSBIGDGJNA-N
[SMILES]

C([C@@H]1[C@]2([H])CCC#CCC[C@]12[H])OC(=O)ON1C(CCC1=O)=O |&1:1,2,10,r|
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Description]

(1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-ylmethyl Succinimidyl Carbonate is a Succinimidyl ester/NHS functionalized cyclooctyne derivative for the addition of the cyclooctyne moiety into amine containing compounds or biomolecules. The BCN group can react with azide-tagged biomolecules under copper free condition.
[Uses]

endo-BCN-NHS carbonate contains BCN group. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.
[reaction suitability]

reaction type: click chemistry
reagent type: cross-linking reagent
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