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1-(2-Aminophenyl)pyrrole, 98+%, Thermo Scientific Chemicals
Catalog number: L06887.03
1 g, Each
Thermo Scientific Chemicals
1-(2-Aminophenyl)pyrrole, 98+%, Thermo Scientific Chemicals
Catalog number: L06887.03
1 g, Each
Quantity
Catalog number: L06887.03
also known as L06887-03
Price (EUR)
21,78 Online price
24,20
Each
Quantity
-
Chemical Identifiers
CAS
6025-60-1
IUPAC Name
2-(1H-pyrrol-1-yl)aniline
Molecular Formula
C10H10N2
InChI Key
GDMZHPUPLWQIBD-UHFFFAOYSA-N
SMILES
NC1=CC=CC=C1N1C=CC=C1
Specifications
Specification SheetForm
Crystals or powder or crystalline powder
Identification (FTIR)
Conforms
Appearance (Color)
White to cream to pale brown or pale yellow
Assay (GC)
≥98.0%
Melting Point (clear melt)
93.5-99.5?C
Description
1-(2-Aminophenyl)pyrrole is used in the synthesis of 4-substituted pyrrolo[1,2-a]quinoxaline derivatives. It participates in Pt(IV)-catalyzed hydroamination triggered cyclization reaction to yield fused pyrrolo [1,2-a] quinoxalines. It is also used as primary and secondary intermediates. They act as antileishmanial agents.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
1-(2-Aminophenyl)pyrrole is used in the synthesis of 4-substituted pyrrolo[1,2-a]quinoxaline derivatives. It participates in Pt(IV)-catalyzed hydroamination triggered cyclization reaction to yield fused pyrrolo [1,2-a] quinoxalines. It is also used as primary and secondary intermediates. They act as antileishmanial agents.
Solubility
Insoluble in water.
Notes
Incompatible materials are oxidizing agents, acids, Acid chlorides, Acid anhydrides, Chloroformates. Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
1-(2-Aminophenyl)pyrrole is used in the synthesis of 4-substituted pyrrolo[1,2-a]quinoxaline derivatives. It participates in Pt(IV)-catalyzed hydroamination triggered cyclization reaction to yield fused pyrrolo [1,2-a] quinoxalines. It is also used as primary and secondary intermediates. They act as antileishmanial agents.
Solubility
Insoluble in water.
Notes
Incompatible materials are oxidizing agents, acids, Acid chlorides, Acid anhydrides, Chloroformates. Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
RUO – Research Use Only
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Safety and Handling
Classification of the substance or mixture
CLP classification - Regulation(EC) No 1272/2008
Acute oral toxicity
Category 4
Acute dermal toxicity
Category 4
Acute Inhalation Toxicity - Dusts and Mists
Category 4
Skin Corrosion/Irritation
Category 2
Serious Eye Damage/Eye Irritation
Category 2
Specific target organ toxicity - (single exposure)
Category 3
Label Elements
Signal Word
Warning
Hazard Statements
H302 + H312 + H332 - Harmful if swallowed, in contact with skin or if inhaled
H315 - Causes skin irritation
H319 - Causes serious eye irritation
H335 - May cause respiratory irritation
Precautionary Statements
P261 - Avoid breathing dust/fume/gas/mist/vapors/spray
P280 - Wear protective gloves/protective clothing/eye protection/face protection
P301 + P312 - IF SWALLOWED: Call a POISON CENTER or doctor/physician if you feel unwell
P304 + P340 - IF INHALED: Remove person to fresh air and keep comfortable for breathing
P305 + P351 + P338 - IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing
P280 - Wear protective gloves/protective clothing/eye protection/face protection
P302 + P352 - IF ON SKIN: Wash with plenty of soap and water