CAS 5407-51-2

2,6-Benzothiazolediamine

Description:

2,6-Benzothiazolediamine, also known as benzothiazole-2,6-diamine, is an organic compound characterized by its benzothiazole structure, which consists of a benzene ring fused to a thiazole ring. This compound typically appears as a solid and is known for its potential applications in various fields, including materials science and pharmaceuticals. It exhibits properties such as good thermal stability and solubility in organic solvents, making it suitable for use in rubber and polymer industries as a vulcanization accelerator. Additionally, 2,6-benzothiazolediamine can act as a reducing agent and is involved in the synthesis of various organic compounds. Its chemical reactivity is influenced by the presence of amino groups, which can participate in various chemical reactions, including nucleophilic substitutions. Safety considerations should be taken into account, as it may pose health risks upon exposure. Overall, 2,6-benzothiazolediamine is a versatile compound with significant industrial relevance.

Formula: C₇H₇N₃S

InChI: InChI=1S/C7H7N3S/c8-4-1-2-5-6(3-4)11-7(9)10-5/h1-3H,8H2,(H2,9,10)

InChI key: InChIKey=HYBCFWFWKXJYFT-UHFFFAOYSA-N

SMILES: NC1=NC=2C(S1)=CC(N)=CC2

Synonyms:

• 2,6-Benzothiazolediamine
• 2,6-Diaminobenzothiazole
• Benzothiazole, 2,6-diamino-
• NSC 5436
• 1,3-Benzothiazole-2,6-diamine

benzothiazole-2,6-diamine

CAS: 5407-51-2

Formula: C₇H₇N₃S

Purity: 98%

Color and Shape: Solid

Molecular weight: 165.2156

Ref: IN-DA00DCX4

1,3-benzothiazole-2,6-diamine

CAS: 5407-51-2

1,3-benzothiazole-2,6-diamine

Purity: ≥95%

Molecular weight: 165.22g/mol

Ref: 54-OR480547

Benzothiazole-2,6-diamine

CAS: 5407-51-2

Formula: C₇H₇N₃S

Purity: 95%

Color and Shape: Solid, Light grey powder

Molecular weight: 165.21

Ref: 10-F029954

1,3-Benzothiazole-2,6-diamine

CAS: 5407-51-2

1,3-Benzothiazole-2,6-diamine (1BDA) is a heterobicyclic compound. It has been shown to have anticancer effects in vitro and in vivo. 1BDA has been shown to inhibit the growth of cancer cells without harming normal cells. The mechanism of action is not well understood but may involve the inhibition of gyrase and topoisomerase enzymes, which are responsible for DNA replication and repair. 1BDA also inhibits dopamine 3 (D3) hydroxylase, which converts dopamine into norepinephrine. Norepinephrine is a neurotransmitter that regulates blood pressure and heart rate. Dopamine D3 receptor antagonists have been investigated as potential antihypertensive drugs and antipsychotics. 1BDA has also been shown to be a potentiodynamic polarization inhibitor which decreases corrosion rates in organic solvents such as chloroformate, acetone, and ethanol.

Formula: C₇H₇N₃S

Purity: Min. 95%

Molecular weight: 165.22 g/mol

Ref: 3D-FB117013