CAS 494833-75-9

tert-butyl (5-bromothiophen-3-yl)carbamate

Description:

Tert-butyl (5-bromothiophen-3-yl)carbamate is an organic compound characterized by its carbamate functional group, which is derived from the reaction of an amine with a carbonyl compound. This substance features a tert-butyl group, providing steric hindrance and enhancing its lipophilicity, which can influence its solubility and reactivity. The presence of the 5-bromothiophen-3-yl moiety introduces a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur, contributing to the compound's electronic properties and potential biological activity. The bromine atom serves as a good leaving group and can participate in further chemical transformations. This compound may exhibit interesting pharmacological properties, making it of interest in medicinal chemistry. Its stability, reactivity, and interactions with biological systems can be influenced by the steric and electronic effects of the substituents present. Overall, tert-butyl (5-bromothiophen-3-yl)carbamate is a versatile compound with potential applications in various fields, including pharmaceuticals and agrochemicals.

Formula: C₉H₁₂BrNO₂S

InChI: InChI=1/C9H12BrNO2S/c1-9(2,3)13-8(12)11-6-4-7(10)14-5-6/h4-5H,1-3H3,(H,11,12)

SMILES: CC(C)(C)OC(=Nc1cc(Br)sc1)O

Synonyms:

• carbamic acid, N-(5-bromo-3-thienyl)-, 1,1-dimethylethyl ester
• tert-Butyl (5-bromo-3-thienyl)carbamate
• Tert-Butyl 5-Bromothiophen-3-Ylcarbamate

2-Bromo-4-(N-tert-butyloxycarbonylamino)thiophene

CAS: 494833-75-9

Formula: C₉H₁₂BrNO₂S

Purity: 97%

Color and Shape: Solid

Molecular weight: 278.1661

Ref: IN-DA00DD5E

2-Bromo-4-(N-tert-butyloxycarbonylamino)thiophene

CAS: 494833-75-9

2-Bromo-4-(N-tert-butyloxycarbonylamino)thiophene

Purity: 97%

Molecular weight: 278.17g/mol

Ref: 54-OR1036497

3-N-Boc-Amino-5-bromothiophene

CAS: 494833-75-9

Formula: C₉H₁₂BrNO₂S

Purity: 97%

Color and Shape: Solid

Molecular weight: 278.16

Ref: 10-F048401