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CS-W001157 4
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(S)-4-Bromo-2,3-dihydro-1H-inden-1-ol

  • CAS No. 83808-19-9

  • Cat. No. CS-0047467
  • Purity≥97%
  • MDL No.None
  • HazMat Fee +

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    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)-4-Bromo-2,3-dihydro-1H-inden-1-ol|CS-0047467

Structure of 83808-19-9

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Description

(S)-4-Bromo-2,3-dihydro-1H-inden-1-ol is a chiral building block featuring a stereodefined hydroxyl group and a bromine substituent at the 4-position. This configuration enables selective transformations in asymmetric synthesis, particularly in the construction of complex indane derivatives. The molecule exhibits bench-stable handling characteristics and compatibility with diverse reaction conditions.

Application

(S)-4-Bromo-2,3-dihydro-1H-inden-1-ol serves as a stereochemically defined building block for the synthesis of chiral indenyl scaffolds. Its stable bicyclic structure and pendant hydroxyl group enable facile functionalization via substitution or coupling reactions. The bromo substituent facilitates Pd-catalyzed cross-coupling, while the alcohol supports selective derivatization or protection. This compound offers predictable reactivity in standard organic transformations, making it a reliable intermediate for medicinal chemistry and process development workflows.

General Information

  • CAS No. 83808-19-9
  • Cat. No. CS-0047467
  • Purity ≥97%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₉H₉BrO
  • Molecular Weight 213.07
  • Synonym(s) (S)-4-bromo-indan-1-ol
  • SMILES BrC1=CC=CC2=C1CC[C@@H]2O

Computational Chemistry Data

  • TPSA   20.23
  • LogP   2.4287
  • 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 : H315-H319-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501

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