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886506-09-8

(4-METHOXY-PHENYL)-PYRROLIDIN-3-YL-AMINE is a chemical compound belonging to the pyrrolidine class, characterized by a molecular formula of C13H18N2O. It features a substituted phenyl group and a pyrrolidin-3-yl-amine group, which may contribute to its potential biological activities and applications in pharmaceutical research and drug development.

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  • 886506-09-8 Structure

  • Basic information

    1. Product Name: (4-METHOXY-PHENYL)-PYRROLIDIN-3-YL-AMINE
    2. Synonyms: (4-METHOXY-PHENYL)-PYRROLIDIN-3-YL-AMINE;N-(4-methoxyphenyl)pyrrolidin-3-amine
    3. CAS NO:886506-09-8
    4. Molecular Formula: C11H16N2O
    5. Molecular Weight: 192.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 886506-09-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (4-METHOXY-PHENYL)-PYRROLIDIN-3-YL-AMINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4-METHOXY-PHENYL)-PYRROLIDIN-3-YL-AMINE(886506-09-8)
    11. EPA Substance Registry System: (4-METHOXY-PHENYL)-PYRROLIDIN-3-YL-AMINE(886506-09-8)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 886506-09-8(Hazardous Substances Data)

886506-09-8 Usage

Uses

Used in Pharmaceutical Research:
(4-METHOXY-PHENYL)-PYRROLIDIN-3-YL-AMINE is used as a research compound for exploring its potential biological activities and applications in drug development. Its unique structural features may offer insights into the design of new therapeutic agents.
Used in Drug Development:
(4-METHOXY-PHENYL)-PYRROLIDIN-3-YL-AMINE is utilized as a starting material or intermediate in the synthesis of pharmaceuticals, potentially leading to the discovery of new drugs with novel mechanisms of action.
Further research is necessary to fully understand the properties and potential uses of (4-METHOXY-PHENYL)-PYRROLIDIN-3-YL-AMINE, as its applications in different industries may vary based on its biological activities and chemical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 886506-09-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,5,0 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 886506-09:
(8*8)+(7*8)+(6*6)+(5*5)+(4*0)+(3*6)+(2*0)+(1*9)=208
208 % 10 = 8
So 886506-09-8 is a valid CAS Registry Number.

886506-09-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-Methoxyphenyl)pyrrolidin-3-amine

1.2 Other means of identification

Product number -
Other names -

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:886506-09-8 SDS

886506-09-8Upstream product

886506-09-8Downstream Products

886506-09-8Relevant articles and documents

tert-Butyl 3-Diazo-2-oxopyrrolidine-1-carboxylate – A New Reagent for Introduction of the 2-Oxopyrrolidin-3-yl Motif via RhII-Catalyzed X–H Insertion Reactions

Zhukovsky, Daniil,Dar'in, Dmitry,Krasavin, Mikhail

, p. 3013 - 3018 (2020)

tert-Butyl 3-diazo-2-oxopyrrolidine-1-carboxylate synthesized on multigram scale has been employed to introduce a privileged NH-2-pyrrolidone moiety via oxygen, sulfur and nitrogen atom to partner molecules via RhII-catalyzed X–H insertion followed by Boc group removal. Further manipulation of pyrrolidine moiety has been exemplified.

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