CAS 52191-26-1

2-chloro-N-[2-(1H-indol-3-yl)ethyl]acetamide

Description:

2-Chloro-N-[2-(1H-indol-3-yl)ethyl]acetamide, with the CAS number 52191-26-1, is a chemical compound characterized by its unique structure that includes a chloro group, an indole moiety, and an acetamide functional group. This compound typically appears as a solid or crystalline substance and is soluble in organic solvents. The presence of the indole ring suggests potential biological activity, as indole derivatives are often associated with various pharmacological properties. The chloro substituent may influence the compound's reactivity and interaction with biological targets. In terms of safety, like many chemical substances, it should be handled with care, as it may pose health risks if inhaled, ingested, or absorbed through the skin. Its specific applications can vary, but it may be of interest in medicinal chemistry and drug development due to its structural features. As with any chemical, proper safety protocols should be followed when handling this compound in a laboratory setting.

Formula: C₁₂H₁₃ClN₂O

InChI: InChI=1/C12H13ClN2O/c13-7-12(16)14-6-5-9-8-15-11-4-2-1-3-10(9)11/h1-4,8,15H,5-7H2,(H,14,16)

SMILES: c1ccc2c(c1)c(CCN=C(CCl)O)c[nH]2

Synonyms:

• 52191-26-1
• T56 Bmj D2Mv1G
• Tryptamine, N-chloroacetyl-
• 2-Chloro-N-[2-(1H-indol-3-yl)ethyl]acetamide

3-(2-(Chloroacetamido)ethyl)indole

CAS: 52191-26-1

Formula: C₁₂H₁₃ClN₂O

Purity: 98%

Color and Shape: Solid

Molecular weight: 236.6974

Ref: IN-DA00DDXY

2-Chloro-N-[2-(1H-indol-3-yl)ethyl]acetamide

CAS: 52191-26-1

2-Chloro-N-[2-(1H-indol-3-yl)ethyl]acetamide

Formula: C₁₂H₁₃ClN₂O

Purity: 98%

Color and Shape: powder

Molecular weight: 236.70g/mol

Ref: 54-OR8384

N-(2-(1H-Indol-3-yl)ethyl)-2-chloroacetamide

CAS: 52191-26-1

Purity: 98%

Molecular weight: 236.6999969

Ref: 10-F689571

2-Chloro-N-[2-(1H-indol-3-yl)ethyl]acetamide

CAS: 52191-26-1

2-Chloro-N-[2-(1H-indol-3-yl)ethyl]acetamide is a synthetic organoheterocyclic compound with the chemical formula of CHClNO. It is the chloro analog of indole. This compound has been used in the synthesis of spengler diketopiperazines and other analogues. 2-Chloro-N-[2-(1H-indol-3-yl)ethyl]acetamide has been shown to react with primary amines, such as piperidine, in an alkylation reaction to form substituted indoles. The nitrogen atom on 2CNEA can be acylated or cyclized to form functionalized derivatives, such as N-[1-(4-chlorophenyl)ethyl]-2-(1H-indol-3-yl)ethanamine (4CNEAE).

Formula: C₁₂H₁₃ClN₂O

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 236.7 g/mol

Ref: 3D-FC127634