(1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-ylmethanol - for Copper-free Click Chemistry , CAS No.1263166-90-0

CAS: 1263166-90-0 Cat. No.: R485486 Molecular Weight: 150.22 Beilstein Registry Number: 21037713 EC Number: 964-382-9

GRADE & PURITY for Copper-free Click Chemistry

Synonyms

exo BCN-H | exo-Bicyclo[6.1.0]non-4-yn-9-ylmethanol | rel-(1R,8S,9s)-Bicyclo[6.1.0]non-4-yn-9-ylmethanol | [(1R,8S,9S)-bicyclo[6.1.0]non-4-yn-9-yl]methanol | Bicyclo[6.1.0]non-4-yne-9-methanol, (1alpha,8alpha,9alpha)- | MFCD19705414 | ((1R,8S,9r)-Bicyclo[

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Overview

Description

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.

Specifications

Synonyms

exo BCN-H | exo-Bicyclo[6.1.0]non-4-yn-9-ylmethanol | rel-(1R, 8S, 9s)-Bicyclo[6.1.0]non-4-yn-9-ylmethanol | [(1R, 8S, 9S)-bicyclo[6.1.0]non-4-yn-9-yl]methanol | Bicyclo[6.1.0]non-4-yne-9-methanol, (1alpha, 8alpha, 9alpha)- | MFCD19705414 | ((1R, 8S, 9r)-Bicyclo[

Specifications & Purity

for Copper-free Click Chemistry

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Names and Identifiers

• Canonical Smiles: C1CC2C(C2CO)CCC#C1
• IUPAC Name: [(1S,8R)-9-bicyclo[6.1.0]non-4-ynyl]methanol
• InChIKey: NSVXZMGWYBICRW-ULKQDVFKSA-N
• INCHI: 1S/C10H14O/c11-7-10-8-5-3-1-2-4-6-9(8)10/h8-11H,3-7H2/t8-,9+,10?
• Isomeric SMILES: C1C[C@@H]2[C@@H](C2CO)CCC#C1
• Molecular Weight: 150.22
• Beilstein: 21037713
• Reaxy-Rn: 22600095
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=22600095&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Class Organooxygen compounds
      • Subclass Alcohols and polyols

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Class: Organooxygen compounds
• Subclass: Alcohols and polyols
• Intermediate Tree Nodes: Not available
• Direct Parent: Primary alcohols
• Alternative Parents: Hydrocarbon derivatives
• Molecular Framework: Aliphatic homopolycyclic compounds
• Substituents: Hydrocarbon derivative - Primary alcohol - Aliphatic homopolycyclic compound
• Description: This compound belongs to the class of organic compounds known as primary alcohols. These are compounds comprising the primary alcohol functional group, with the general structure RCOH (R=alkyl, aryl).
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Melt Point(°C): 64 °C
• Molecular Weight: 150.220 g/mol
• XLogP3: 1.900
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 150.104 Da
• Monoisotopic Mass: 150.104 Da
• Topological Polar Surface Area: 20.200 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 189.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 2
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1