(1R)-(-)-10-Camphorsulfonyl chloride - ≥97% , CAS No.39262-22-1

CAS: 39262-22-1 Cat. No.: C102453 Molecular Weight: 250.74 Beilstein Registry Number: 3205975 EC Number: 628-057-2

GRADE & PURITY ≥97%

Synonyms

MFCD00064155 | C10H15ClO3S | F0001-2351 | A824492 | 10-Camphorsulfonyl chloride | (1R)-(-)-10-Camphorsulfonyl chloride, for chiral derivatization, 97.0-103.0% (AT) | SCHEMBL12706679 | FD1220 | L-10-Camphorsulfonyl chloride | AS-19113 | L-(-)-10-Camphorsul

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Synonyms

MFCD00064155 | C10H15ClO3S | F0001-2351 | A824492 | 10-Camphorsulfonyl chloride | (1R)-(-)-10-Camphorsulfonyl chloride, for chiral derivatization, 97.0-103.0% (AT) | SCHEMBL12706679 | FD1220 | L-10-Camphorsulfonyl chloride | AS-19113 | L-(-)-10-Camphorsul

Specifications & Purity

≥97%

Storage

Store at 2-8°C, Argon charged

Shipped In

Wet ice

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

Purity

≥97%

Names and Identifiers

• Canonical Smiles: CC1(C2CCC1(C(=O)C2)CS(=O)(=O)Cl)C
• IUPAC Name: [(1R,4S)-7,7-dimethyl-2-oxo-1-bicyclo[2.2.1]heptanyl]methanesulfonyl chloride
• InChIKey: BGABKEVTHIJBIW-XVKPBYJWSA-N
• INCHI: 1S/C10H15ClO3S/c1-9(2)7-3-4-10(9,8(12)5-7)6-15(11,13)14/h7H,3-6H2,1-2H3/t7-,10-/m0/s1
• Isomeric SMILES: CC1([C@H]2CC[C@@]1(C(=O)C2)CS(=O)(=O)Cl)C
• WGK Germany: 3
• UN Number: 3261
• Molecular Weight: 250.74
• Beilstein: 3205975
• Reaxy-Rn: 525867
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=525867&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Class Prenol lipids
      • Subclass Monoterpenoids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Class: Prenol lipids
• Subclass: Monoterpenoids
• Intermediate Tree Nodes: Not available
• Direct Parent: Bicyclic monoterpenoids
• Alternative Parents: Sulfonyls Sulfonyl chlorides Organosulfonic acids and derivatives Ketones Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic homopolycyclic compounds
• Substituents: Bicyclic monoterpenoid - Bornane monoterpenoid - Sulfonyl - Sulfonyl halide - Sulfonyl chloride - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Carbonyl group - Aliphatic homopolycyclic compound
• Description: This compound belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.
• 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

• Solubility: Soluble in Toluene
• Sensitivity: Moisture sensitive.Heat sensitive
• Specific Rotation[α]: -29.5 ° (C=1, CHCl3)
• Melt Point(°C): 66-68°C
• Molecular Weight: 250.740 g/mol
• XLogP3: 1.800
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 250.043 Da
• Monoisotopic Mass: 250.043 Da
• Topological Polar Surface Area: 59.600 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 407.000
• 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

References

1. Zixing Wang, Yuxin Fan, Hong Chen, Xiang Chen, Dexuan Cai, Xihao Tang, Shengrun Zheng, Jun Fan, Songliang Cai, Weiguang Zhang.  (2025)  Preparation and resolution performances of chiral stationary phases based on spherical covalent organic frameworks with various zeta potentials.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:40435717] [10.1016/j.chroma.2025.466087]