CAS 143262-10-6

1-Boc-indoline

Description:

1-Boc-indoline, with the CAS number 143262-10-6, is a chemical compound characterized by the presence of an indoline structure, which is a bicyclic compound consisting of a fused benzene and pyrrole ring. The "Boc" in its name refers to the tert-butyloxycarbonyl (Boc) protecting group, commonly used in organic synthesis to protect amines during chemical reactions. This compound typically appears as a solid and is soluble in organic solvents such as dichloromethane and dimethyl sulfoxide. Its molecular structure allows for various functionalization reactions, making it valuable in the synthesis of pharmaceuticals and other organic compounds. The presence of the Boc group enhances the stability of the indoline moiety and facilitates its use in peptide synthesis and other applications where amine protection is necessary. Overall, 1-Boc-indoline serves as an important intermediate in organic chemistry, particularly in the development of biologically active molecules.

Formula: C₁₃H₁₇NO₂

InChI: InChI=1/C13H17NO2/c1-13(2,3)16-12(15)14-9-8-10-6-4-5-7-11(10)14/h4-7H,8-9H2,1-3H3

SMILES: CC(C)(C)OC(=O)N1CCc2ccccc12

Synonyms:

• 1-(tert-Butoxycarbonyl)indoline
• tert-Butyl indoline-1-carboxylate
• tert-butyl 2,3-dihydro-1H-indole-1-carboxylate

Tert-Butyl Indoline-1-Carboxylate

CAS: 143262-10-6

Tert-Butyl Indoline-1-Carboxylate

Formula: C₁₃H₁₇NO₂

Purity: 98%

Molecular weight: 219.28

Ref: 54-OR1015155

1-BOC-INDOLINE

CAS: 143262-10-6

Formula: C₁₃H₁₇NO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 219.2796

Ref: IN-DA003E2B

tert-Butyl indoline-1-carboxylate

CAS: 143262-10-6

tert-Butyl indoline-1-carboxylate

Formula: C₁₃H₁₇NO₂

Purity: 98%

Molecular weight: 219.28

Ref: IN-DG57203

tert-Butyl indoline-1-carboxylate

CAS: 143262-10-6

Purity: 98%

Molecular weight: 219.2839966

Ref: 10-F604265

tert-Butyl indoline-1-carboxylate

CAS: 143262-10-6

Tert-butyl indoline-1-carboxylate is a nitrogenous compound that contains a tertiary amine group. It can be synthesized by reacting 2,5-dimethoxybenzyl alcohol with lithium and tetramethylethylenediamine. Tert-butyl indoline-1-carboxylate has been shown to be cytotoxic in vitro and in vivo. It can inhibit the growth of cancer cells by inhibition of DNA synthesis, RNA synthesis, protein synthesis, and lipid biosynthesis. Tert-butyl indoline-1-carboxylate also exhibits potent antiangiogenic effects and induces apoptosis in endothelial cells.

Formula: C₁₃H₁₇NO₂

Purity: Min. 95%

Molecular weight: 219.28 g/mol

Ref: 3D-TFA26210