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Benzothiadiazoles

Organic heterocyclic compounds that consist of a benzene fused with a thiadiazole ring; thiadiazoles have a five-membered ring that contains two nitrogen atoms, one sulfur atoms, and two double bonds.
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2-[(7-Bromo-2,1,3-benzothiadiazol-4-yl)methylene]malononitrile 98.0+%, TCI America™

CAS: 1335150-10-1 Molecular Formula: C10H3BrN4S Molecular Weight (g/mol): 291.126 MDL Number: MFCD23704429 InChI Key: ZNWYPDKJWGLSQU-UHFFFAOYSA-N PubChem CID: 89394801 IUPAC Name: 2-[(4-bromo-2,1,3-benzothiadiazol-7-yl)methylidene]propanedinitrile SMILES: C1=C(C2=NSN=C2C(=C1)Br)C=C(C#N)C#N

PubChem CID 89394801
CAS 1335150-10-1
Molecular Weight (g/mol) 291.126
MDL Number MFCD23704429
SMILES C1=C(C2=NSN=C2C(=C1)Br)C=C(C#N)C#N
IUPAC Name 2-[(4-bromo-2,1,3-benzothiadiazol-7-yl)methylidene]propanedinitrile
InChI Key ZNWYPDKJWGLSQU-UHFFFAOYSA-N
Molecular Formula C10H3BrN4S
2

Medchemexpress LLC S-[2-[6-[[4-[3-(dimethylamino)propoxy]phenyl]sulfonylamino]-3-pyridinyl]-2-oxoethyl] ethanethioate | 940943-37-3 | MFCD19690928 | 98.1% | 451.56 | C20H25N3O5S2 | 10 MG
SDP

KD 5170 is a small-molecule pan inhibitor of histone deacetylases (HDACs) that demonstrates broad-spectrum antitumor activity in vitro and in vivo. It is offered for laboratory research use and includes recommended solubility and storage guidance for experimental applications.

  • Pan inhibitor of histone deacetylases (HDACs).
  • Demonstrates broad-spectrum antitumor activity in vitro and in vivo.
  • High purity (≈98.1%).
  • Molecular formula C20H25N3O5S2; molecular weight 451.56.
  • Soluble in DMSO (100 mg/mL); in vivo formulations documented at 2.5 mg/mL in common vehicles.
  • Store sealed at 4°C; in solvent store at -80°C for long-term stability.

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