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CS-W001157 4
Total: USD 88.00

(S)-2,3-Dihydro-1H-inden-1-ol

  • CAS No. 25501-32-0

  • Cat. No. CS-W013372
  • Purity≥97%
  • MDL No.MFCD00064165
  • HazMat Fee +

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    Each bottle is packed as an Excepted Quantity, with a maximum of 1g for items in class 6.1 packing group I or II, and up to 25g for all other hazardous materials.

    If shipping is charged to your FedEx account, the HazMat fee will be billed directly by the courier. Otherwise, the fee will be included on your invoice. To help you avoid the HazMat fee, we can package a 5g order of a class 6.1 packing group I or II material as five separate 1g units, and a 100g order of any other dangerous good as four 25g units. This packaging adjustment will be made unless you instruct otherwise on your purchase order. Below, you will find the fee schedule from FedEx for handling hazardous materials.

    Type
    HazMat Fee
    Excepted Quantity $0.00
    FedEx Limited Quantities Ground $0.00
    Hazmat Ground shipping $50.00+
    Inaccessible (Haz class 6.1 or 9), Domestic $68.00+
    Accessible (Haz class 3, 4, 5 or 8), Domestic $158.00+
    Inaccessible (Haz class 6.1 or 9), International $108.00+
    Accessible (Haz class 3, 4, 5 or 8), International $238.00+

    An item is classified as a dangerous good if our website displays Hazardous Material (HazMat) information for it.

    There is a HazMat shipping fee for each item that qualifies as a dangerous good. Please contact our quotation team via email to confirm the details.

*For research and further manufacturing use only, not for direct human use.

(S)-2,3-Dihydro-1H-inden-1-ol|CS-W013372

Structure of 25501-32-0

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Description

(S)-2,3-Dihydro-1H-inden-1-ol is a chiral, bench-stable building block featuring a hydroxyl group at the benzylic position of a saturated indene core. This configuration enables stereoselective transformations in asymmetric synthesis, particularly in the construction of complex polycyclic architectures. The molecule's rigid, planar framework supports predictable reactivity in transition-metal-catalyzed coupling and oxidation processes.

Application

(S)-2,3-Dihydro-1H-inden-1-ol serves as a chiral building block for asymmetric synthesis, offering a rigid, enantiomerically pure scaffold with a benzylic hydroxyl group. Its stability and compatibility with standard functional group transformations enable reliable use in medicinal chemistry and natural product synthesis. The molecule facilitates stereoselective derivatization and acts as a key intermediate in the construction of complex heterocyclic frameworks and bioactive compounds.

General Information

  • CAS No. 25501-32-0
  • Cat. No. CS-W013372
  • Purity ≥97%
  • MDL No. MFCD00064165
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₁₀O
  • Molecular Weight 134.18
  • Synonym(s) (S)-(+)-1-Indanol
  • SMILES O[C@H]1CCC2=C1C=CC=C2

Computational Chemistry Data

  • TPSA   20.23
  • LogP   1.6662
  • H_Acceptors   1
  • H_Donors   1
  • Rotatable_Bonds   0

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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