5-(Bromomethyl)-2,1,3-benzothiadiazole is a heterocyclic compound characterized by the presence of a benzothiadiazole core, which consists of a benzene ring fused to a thiadiazole ring. This compound features a bromomethyl group at the 5-position, which enhances its reactivity and potential for further chemical modifications. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of the bromine atom introduces electrophilic characteristics, making it useful in various synthetic applications, including the development of pharmaceuticals and agrochemicals. Additionally, the benzothiadiazole moiety is known for its applications in materials science, particularly in organic electronics and photonic devices due to its electronic properties. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, this compound is of interest in both synthetic organic chemistry and materials science due to its unique structural features and reactivity.

5-(bromomethyl)-2,1,3-benzothiadiazole

65858-50-6: 5-(Bromomethyl)-2,1,3-benzothiadiazole is a heterocyclic compound characterized by the presence of a benzothiadiazole core, which consists of a benzene ring fused to a thiadiazole ring. This compound features a bromomethyl group at the 5-position, which enhances its reactivity and potential for further chemical modifications. It is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. The presence of the bromine atom introduces electrophilic characteristics, making it useful in various synthetic applications, including the development of pharmaceuticals and agrochemicals. Additionally, the benzothiadiazole moiety is known for its applications in materials science, particularly in organic electronics and photonic devices due to its electronic properties. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, this compound is of interest in both synthetic organic chemistry and materials science due to its unique structural features and reactivity.

CAS 65858-50-6

5-(bromomethyl)-2,1,3-benzothiadiazole

5-(Bromomethyl)benzo[c][1,2,5]thiadiazole

Ref: IN-DA00FD3P

5-(Bromomethyl)benzo[c][1,2,5]thiadiazole

Ref: 10-F217641

5-(Bromomethyl)-2,1,3-benzothiadiazole

Ref: 54-OR23129