CAS 182344-70-3

TERT-BUTYL 5-BROMOINDOLE-1-CARBOXYLATE

Description:

Tert-butyl 5-bromoindole-1-carboxylate is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. The presence of a tert-butyl group enhances its lipophilicity, making it more soluble in organic solvents. The bromine atom at the 5-position of the indole ring introduces a halogen substituent, which can participate in various chemical reactions, including nucleophilic substitutions and cross-coupling reactions. The carboxylate functional group, derived from the carboxylic acid, is typically involved in esterification reactions and can serve as a reactive site for further functionalization. This compound is of interest in medicinal chemistry and organic synthesis due to its potential biological activity and utility in the development of pharmaceuticals. Its molecular structure and reactivity make it a valuable intermediate in the synthesis of more complex molecules. As with many organic compounds, proper handling and safety precautions should be observed due to potential hazards associated with its use.

Formula: C₁₃H₁₄BrNO₂

InChI: InChI=1/C13H14BrNO2/c1-13(2,3)17-12(16)15-7-6-9-8-10(14)4-5-11(9)15/h4-8H,1-3H3

SMILES: CC(C)(C)OC(=O)n1ccc2cc(ccc12)Br

Synonyms:

• 5-Bromo-1-(Tert-Butoxycarbonyl)-1H-Indole
• Tert-Butyl 5-Bromo-1H-Indole-1-Carboxylate
• N-Boc-5-bromoindole
• 1-BOC-5-bromoindole
• N-Boc-5-bromoindole 13C6
• TERT-BUTYL 5-BROMOINDOLE-1-CARBOXYLATE
• 5-Bromo-1-tert-butoxycarbonylindole
• 5-Bromo-1-(t-Butoxycarbonyl)-1H-indole
• 5-bromo-1-indolecarboxylic acid tert-butyl ester
• 1H-Indole-1-carboxylic acid, 5-bromo-, 1,1-dimethylethyl ester
• 1-Boc-5-bromo-1H-indole

tert-Butyl 5-Bromo-1H-indole-1-carboxylate

CAS: 182344-70-3

Formula: C₁₃H₁₄BrNO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 296.164

Ref: 10-F067481

1-BOC-5-bromoindole

CAS: 182344-70-3

Formula: C₁₃H₁₄BrNO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 296.1598

Ref: IN-DA0023OS

tert-Butyl5-bromo-1H-indole-1-carboxylate

CAS: 182344-70-3

tert-Butyl5-bromo-1H-indole-1-carboxylate

Purity: ≥98%

Molecular weight: 296.16g/mol

Ref: 54-BUP19660

tert-Butyl5-bromo-1H-indole-1-carboxylate

CAS: 182344-70-3

Tert-Butyl5-bromo-1H-indole-1-carboxylate (N-Boc-5-bromoindole) is an indole derivative with therapeutic potential for pain, inflammation, and other conditions.

Formula: C₁₃H₁₄BrNO₂

Purity: 98.16%

Color and Shape: Solid

Molecular weight: 296.16

Ref: TM-T77351

tert-Butyl 5-Bromo-1H-indole-1-carboxylate

CAS: 182344-70-3

Formula: C₁₃H₁₄BrNO₂

Purity: >95.0%(T)(HPLC)

Color and Shape: White to Light yellow powder to crystal

Molecular weight: 296.16

Ref: 3B-B6358

N-Boc-5-bromoindole

CAS: 182344-70-3

N-Boc-5-bromoindole

Purity: 99%

Color and Shape: Solid

Molecular weight: 296.16g/mol

Ref: 54-OR460023

N-Boc-5-bromoindole

CAS: 182344-70-3

N-Boc-5-bromoindole is an aryl boronic acid that is used as a coupling partner in Suzuki and cross-coupling reactions. It has been shown that this compound can be used to modulate the reactivity of aryl bromides and iodides, which makes it suitable for the synthesis of complex molecules. N-Boc-5-bromoindole has been shown to be effective in coupling reactions with a wide variety of functional groups, including hydroboration, miyaura, and cross-coupling reactions.

Formula: C₁₃H₁₄BrNO₂

Purity: Min. 95%

Molecular weight: 296.16 g/mol

Ref: 3D-HHA34470