742678

(1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-ylmethanol

for Copper-free Click Chemistry

• Synonym(s): (1α,8α,9β)-Bicyclo[6.1.0]non-4-yne-9-methanol, endo-9-Hydroxymethylbicyclo[6.1.0]non-4-yne, BCN-OH
• Empirical Formula (Hill Notation): C₁₀H₁₄O
• CAS Number: 1263166-90-0
• Molecular Weight: 150.22
• Beilstein: 21037713
• MDL number: MFCD26142970
• UNSPSC Code: 12352209
• PubChem Substance ID: 329765586
• NACRES: NA.22

Properties

• form: powder
• composition: carbon content, 79.96% ; hydrogen content, 9.39%
• reaction suitability: reaction type: click chemistry; reagent type: linker
• functional group: hydroxyl
• storage temp.: −20°C
• SMILES string: [H][C@@]12[C@@]([C@H]2CO)([H])CCC#CCC1
• InChI: 1S/C10H14O/c11-7-10-8-5-3-1-2-4-6-9(8)10/h8-11H,3-7H2/t8-,9+,10-
• InChI key: NSVXZMGWYBICRW-ILWJIGKKSA-N

Description

Application

Alcohol functionalized cyclooctyne derivative. Cyclooctynes are useful in strain-promoted copper-free azide-alkyne cycloaddition reactions. This strained cyclooctyne will react with azide functionalized compounds or biomolecules without the need for a copper catalyst to result in a stable triazole linkage.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Safety Information

• Storage Class Code: 11 - Combustible Solids
• WGK: WGK 3
• Flash Point(F): Not applicable
• Flash Point(C): Not applicable