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CAS

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29212-49-5

1H-Pyrrol-3-amine(9CI) is a chemical compound that plays a significant role in organic chemistry. It is classified as an amine, which means it contains a basic nitrogen atom with a lone pair, and as a heterocyclic compound, characterized by the presence of at least two different elements in its ring structure. 1H-Pyrrol-3-amine(9CI) features a pyrrole ring, a five-membered aromatic ring with one nitrogen atom, and an amino group (NH2). Due to its reactivity and versatility, 1H-Pyrrol-3-amine(9CI) is frequently utilized in chemical synthesis, particularly for the production of pharmaceuticals and complex organic molecules. It is typically found as a colorless or pale yellow liquid and should be handled with caution due to its potential health and environmental risks.

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  • 29212-49-5 Structure

  • Basic information

    1. Product Name: 1H-Pyrrol-3-amine(9CI)
    2. Synonyms: 1H-Pyrrol-3-amine(9CI);3-AMinopyrrole;1H-Pyrrol-3-aMine
    3. CAS NO:29212-49-5
    4. Molecular Formula: C4H6N2
    5. Molecular Weight: 82.1038
    6. EINECS: N/A
    7. Product Categories: PYRROLE
    8. Mol File: 29212-49-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 258.982 °C at 760 mmHg
    3. Flash Point: 134.248 °C
    4. Appearance: /
    5. Density: 1.172 g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
    8. Solubility: N/A
    9. PKA: 17.68±0.50(Predicted)
    10. CAS DataBase Reference: 1H-Pyrrol-3-amine(9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1H-Pyrrol-3-amine(9CI)(29212-49-5)
    12. EPA Substance Registry System: 1H-Pyrrol-3-amine(9CI)(29212-49-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 29212-49-5(Hazardous Substances Data)

29212-49-5 Usage

Uses

Used in Pharmaceutical Industry:
1H-Pyrrol-3-amine(9CI) is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to form complex organic molecules and contribute to the development of new drugs.
Used in Organic Chemistry Research:
1H-Pyrrol-3-amine(9CI) is used as a reagent in organic chemistry research to explore its reactivity and potential applications in the creation of novel compounds and materials.
Used in Chemical Synthesis:
1H-Pyrrol-3-amine(9CI) is used as a building block in the synthesis of complex organic molecules, leveraging its versatile chemical properties to construct a wide range of chemical structures.

Check Digit Verification of cas no

The CAS Registry Mumber 29212-49-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,2,1 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 29212-49:
(7*2)+(6*9)+(5*2)+(4*1)+(3*2)+(2*4)+(1*9)=105
105 % 10 = 5
So 29212-49-5 is a valid CAS Registry Number.

29212-49-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-Pyrrol-3-amine

1.2 Other means of identification

Product number -
Other names 1H-pyrrol-3-ylamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:29212-49-5 SDS

29212-49-5Synthetic route

3-amino pyrrole
29212-49-5

3-amino pyrrole

1,3-cylohexanedione
504-02-9

1,3-cylohexanedione

5-((1H-benzo[d]imidazol-2-yl)thio)furan-2-carbaldehyde
39689-08-2

5-((1H-benzo[d]imidazol-2-yl)thio)furan-2-carbaldehyde

(+)-9-[5-(1H-benzimidazol-2-ylsulfanyl)-2-furyl]-2,4,5,6,7,9-hexahydropyrrolo[3,4-b]quinolin-8-one

(+)-9-[5-(1H-benzimidazol-2-ylsulfanyl)-2-furyl]-2,4,5,6,7,9-hexahydropyrrolo[3,4-b]quinolin-8-one

Conditions
ConditionsYield
In ethanol for 0.5h; Reflux;12 mg

29212-49-5Upstream product

29212-49-5Downstream Products

29212-49-5Relevant articles and documents

3-aminopyrroles, methods for their synthesis and for their pharmaceutical use

-

, (2008/06/13)

The invention is directed to 3-aminopyrroles of formula I, which are largely new, to methods for the preparation and to their use as medicinal agents and preparations, as well as to anti-convulsive or analgesic preparations containing these 3-aminopyrroles. Disubstituted and monosubstituted amino groups are claimed as 3-amino substituents. The invention pursues the objective of developing largely new 3-aminopyrroles, which have CNS activity, particularly ones which anti-convulsive or analgesic properties, as well as methods for their preparation and their use as medicinal preparations. Pursuant to the invention, the synthesis is carried out by cyclizing open-chain precursors, such as aminoacrylic acid derivative, or by modifying pyrroles.

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