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

CAS: 39262-22-1 Cat. No.: C102453 Peso molecular: 250.74 Beilstein Registry Number: 3205975 Número EC: 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

Sinónimos

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

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Argon charged

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥97%

Nombres e identificadores

• Sonrisas canónicas: 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
• Isómeros SMILES: CC1([C@H]2CC[C@@]1(C(=O)C2)CS(=O)(=O)Cl)C
• WGK Alemania: 3
• Número ONU: 3261
• Peso molecular: 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
    • Clase Prenol lipids
      • Subclass Monoterpenoids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: 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
• Descripción: 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

Propiedades químicas y físicas

• Solubilidad: Soluble in Toluene
• Sensibilidad: Moisture sensitive.Heat sensitive
• Rotación específica [α]: -29.5 ° (C=1, CHCl3)
• Punto de fusión (°C): 66-68°C
• Peso molecular: 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

Referencias

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]