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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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Percent Purity 
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Physical Form 
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Boiling Point 
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Molecular Weight (g/mol)

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Percent Purity

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Physical Form

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Boiling Point

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Search Within Results
Keyword Search:
76 – 90 of 104 results
76

Matrix Scientific 4,7-DIBROMO-2,1,3-BENZOTHIAD-5

4,7-dibromo-2,1,3-benzothiadiazole Mf C6h2br2n2s Mw 293.98 Cas 15155-41-6 Mdl MFCD00658844

ENCOMPASS_PREFERRED
77

eMolecules​ 65858-50-6 | 5-(Bromomethyl)-2,1,3-benzothiadiazole | Combi-Blocks | MFCD00544836 | 229.100 | C7H5BrN2S | 97.000 | BrCc1ccc2nsnc2c1 | 5g | 342867659

5-(Bromomethyl)-2,1,3-benzothiadiazole | Combi-Blocks | 65858-50-6 | MFCD00544836 | 229.100 | C7H5BrN2S | 97.000 | BrCc1ccc2nsnc2c1 | 5g | 342867659

ENCOMPASS_PREFERRED
78

Sigma Aldrich Fine Chemicals Biosciences Tizanidine Related Compound A30536-19-7 | MFCD00465908 | 50mg

Tizanidine Related Compound A | MW:185.63 | 30536-19-7 | MFCD00465908 | 50mg

ENCOMPASS
79

Medchemexpress LLC 2 1 3-BENZOTHIADIAZO 500 mg
SDP

2 1 3-BENZOTHIADIAZO 500MG

ENCOMPASS_PREFERRED
80

Medchemexpress LLC XOMA-213 10 mg
SDP

XOMA-213 10MG

ENCOMPASS_PREFERRED
81

Medchemexpress LLC MEDCHEMEXPRESS LLC
SDP

5000744713 PSB-22034 25MG

ENCOMPASS_PREFERRED
82

Medchemexpress LLC MEDCHEMEXPRESS LLC
SDP

5000745882 PSB-22034 10MM/1ML

ENCOMPASS_PREFERRED
83

Medchemexpress LLC PSB-22034 50 mg
SDP

PSB-22034 50MG

ENCOMPASS_PREFERRED
84

Medchemexpress LLC FAUC 213 | 337972-47-1 | 99.9% | C18H19ClN4 | 50 MG
SDP

FAUC 213 is an orally active and highly selective dopamine D4 receptor complete antagonist with a Ki of 2.2 nM for hD4.4. It shows less activity on D2 and D3 receptors, with Kis of 3.4 μM and 5.3 μM respectively. This compound can cross the blood-brain barrier (BBB) and exhibits atypical antipsychotic characteristics.

  • Highly selective dopamine D4 receptor complete antagonist
  • Orally active
  • Crosses the blood-brain barrier (BBB)
  • Exhibits atypical antipsychotic characteristics
  • Inhibits p5-HT1 (Ki=1.2 μM), p5-HT2 (Ki=0.52 μM), and pα1 (Ki=0.27 μM)
  • Significantly reduces amphetamine-induced locomotor hyperactivity at 30 mg/kg
  • Restores prepulse inhibition reduction caused by apomorphine treatment at 30 mg/kg

ENCOMPASS_PREFERRED
85

Aobchem 4 7-Dibromo-2 1 3-benzothiadiazole | ≥95% | CAS 15155-41-6 | C6H2Br2N2S | 25g

4 7-Dibromo-2 1 3-benzothiadiazole | ≥95% | CAS 15155-41-6 | C6H2Br2N2S | 25g

ENCOMPASS_PREFERRED
86

Aobchem 4 7-Dibromo-2 1 3-benzothiadiazole | ≥95% | CAS 15155-41-6 | C6H2Br2N2S | 100g

4 7-Dibromo-2 1 3-benzothiadiazole | ≥95% | CAS 15155-41-6 | C6H2Br2N2S | 100g

ENCOMPASS_PREFERRED
87

Medchemexpress LLC FAUC 213 | 337972-47-1 | 99.9% | C18H19ClN4 | 10 MM 1 ML
SDP

FAUC 213 is an orally active and highly selective dopamine D4 receptor complete antagonist with a Ki of 2.2 nM for hD4.4. It has less activity on D2 and D3 receptors (Kis of 3.4 μM, 5.3 μM for hD2, hD3, respectively) and can cross the blood-brain barrier (BBB). FAUC 213 exhibits atypical antipsychotic characteristics.

  • Orally active
  • Highly selective dopamine D4 receptor complete antagonist
  • Ki of 2.2 nM for hD4.4
  • Less activity on D2 and D3 receptors (Kis of 3.4 μM, 5.3 μM for hD2, hD3, respectively)
  • Can cross the blood-brain barrier (BBB)
  • Exhibits atypical antipsychotic characteristics

ENCOMPASS_PREFERRED
88

Medchemexpress LLC 2 1 3-BENZOTHIADIAZO 250 mg
SDP

2 1 3-BENZOTHIADIAZO 250MG

ENCOMPASS_PREFERRED
89

Medchemexpress LLC 2 1 3-BENZOTHIADIAZO 1G
SDP

2 1 3-BENZOTHIADIAZO 1G

ENCOMPASS_PREFERRED
90

Medchemexpress LLC MEDCHEMEXPRESS LLC
SDP

5000759837 2 1 3-BENZOTHIADIAZO 100MG

ENCOMPASS_PREFERRED