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    5,7-Dichloro-thiazolo[5,4-d]pyrimidine, CAS 13479-88-4, is in stock from AChemBlock as a research-use peptide coupling reagent.
    Chemical structure of 5,7-Dichloro-thiazolo[5,4-d]pyrimidine , CAS 13479-88-4, AChemBlock F-4048

    5,7-Dichloro-thiazolo[5,4-d]pyrimidine

    Catalog ID: F-4048

    Product Name: 5,7-Dichloro-thiazolo[5,4-d]pyrimidine
    CAS: 13479-88-4
    MDL: MFCD09702027
    Purity: 97%
    Appearance: white to brown powder
    FW: 206.05
    Formula: C₅HCl₂N₃S
    Smiles: ClC1=NC(Cl)=C2N=CSC2=N1
    5,7-Dichloro-thiazolo[5,4-d]pyrimidine 97%, CAS#: 13479-88-4, Cat ID: F-4048, BUILDING BLOCKS, AChemBlock
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    For research use only. We do not sell to patients
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    Packaging:1G List Price: $55 Quantity:
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    Aug 04,2026

    Packaging:5G List Price: $240 Quantity:
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    Aug 04,2026

    Packaging:25G List Price: $895 Quantity:
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    Aug 04,2026

    update on 08-03-2026

    You can click the buttons of HNMR, HPLC, or CoA to view the documents.

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    Safety Information
    Safety Information
    Pictograms GHS07
    Signal Word Warning
    Hazard Statements Causes skin irritation
    Causes serious eye irritation
    May cause respiratory irritation
    Precautionary Statements Avoid breathing dust/fume/gas/mist/vapours/spray.
    Product Information
    Product Information
    Product Information
    Purity 97%
    Appearances white to brown powder
    Storage Store at 0-8 °C
    Shipping Room Temp
    MSDS Download MSDS
    IUPAC Name 5,7-dichlorothiazolo[5,4-d]pyrimidine
    HTS Code 2934990900
    Smiles ClC1=NC(Cl)=C2N=CSC2=N1
    InChiKey XYBGDWLYHQAUQM-UHFFFAOYSA-N
    Product Description 5,7-Dichloro-thiazolo[5,4-d]pyrimidine (CAS 13479-88-4, Catalog ID F-4048) is in stock from AChemBlock. This product is listed for research use and can support medicinal chemistry, organic synthesis, and laboratory research applications. Please contact AChemBlock for quotation, pack size, purity, COA, SDS, and lead-time information.
    Product Application Used as a research-use reagent for peptide synthesis, amide-bond formation, and medicinal chemistry workflows.
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