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CAS

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129540-24-5

2-(2-BROMOPHENYL)-PYRROLIDINE is an organic compound with a molecular structure that features a pyrrolidine ring attached to a bromophenyl group. It is known for its potential applications in the pharmaceutical industry due to its unique chemical properties.

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  • 129540-24-5 Structure

  • Basic information

    1. Product Name: 2-(2-BROMOPHENYL)-PYRROLIDINE
    2. Synonyms: 2-(2-BROMOPHENYL)-PYRROLIDINE;2-(2-bromophenyl)-Pyrrolidine (in HCl form);2-(2-BroMophenyl)pyrrolidine 97%
    3. CAS NO:129540-24-5
    4. Molecular Formula: C10H12BrN
    5. Molecular Weight: 226.11
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 129540-24-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 274℃
    3. Flash Point: 120℃
    4. Appearance: white to beige crystals or crystalline powder
    5. Density: 1.369
    6. Vapor Pressure: 0.00124mmHg at 25°C
    7. Refractive Index: 1.519
    8. Storage Temp.: 2-8°C(protect from light)
    9. Solubility: N/A
    10. PKA: 9.45±0.10(Predicted)
    11. CAS DataBase Reference: 2-(2-BROMOPHENYL)-PYRROLIDINE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-(2-BROMOPHENYL)-PYRROLIDINE(129540-24-5)
    13. EPA Substance Registry System: 2-(2-BROMOPHENYL)-PYRROLIDINE(129540-24-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 36/37/38
    3. Safety Statements: 26-36/37/39
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 129540-24-5(Hazardous Substances Data)

129540-24-5 Usage

Uses

Used in Pharmaceutical Industry:
2-(2-BROMOPHENYL)-PYRROLIDINE is used as a reagent for the preparation of pyrroloisoquinolinone derivatives, which are considered potential antidepressants. Its role in the synthesis process is crucial for developing new and effective treatments for depression.

Check Digit Verification of cas no

The CAS Registry Mumber 129540-24-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,5,4 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 129540-24:
(8*1)+(7*2)+(6*9)+(5*5)+(4*4)+(3*0)+(2*2)+(1*4)=125
125 % 10 = 5
So 129540-24-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO/c1-2-14-11-7-5-10(6-8-11)12-4-3-9-13-12/h5-8,12-13H,2-4,9H2,1H3

129540-24-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-bromophenyl)pyrrolidine

1.2 Other means of identification

Product number -
Other names 2-(2-Bromophenyl)-pyrrolidine

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:129540-24-5 SDS

129540-24-5Relevant articles and documents

(PYRROLIDIN-2-YL)PHENYL DERIVATIVES

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Page/Page column 8, (2010/05/13)

The invention relates to (pyrrolidin-2-yl)phenyl derivatives having the general Formula I wherein R1 is (C1-4)alkyl, halo(C1-4)alkyl, (C1-4)alkyloxy, or halo(C1-4)alkyloxy; R2 is H, (C

( PYRROLIDIN-2 -YL) PHENYL DERIVATIVES FOR USE IN THE TREATMENT OF PAIN

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Page/Page column 19, (2010/06/11)

The invention relates to (pyrrolidin-2-yl)phenyl derivatives having the general Formula (I), wherein R1 is (C1-4)alkyl, halo(C1-4)alkyl, (C1-4)alkyloxy, or halo(C1-4)alkyloxy; R2 is H, (Cs

Pyrroloisoquinoline antidepressants. 3. A focus on serotonin

Maryanoff,Vaught,Shank,McComsey,Costanzo,Nortey

, p. 2793 - 2797 (2007/10/02)

A collection of hexahydropyrroloisoquinoline derivatives (1-22), which represent a class of compounds that inhibit the neuronal uptake of dopamine (DA), norepinephrine (NE), and serotonin (5-HT), was investigated in vivo for serotonin-potentiating propert

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