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(2S)-1-[4-(10,11-dihydro-5H-dibenzo[a,d][7]annulen-5-yl)piperazin-1-yl]-3-(quinolin-5-yloxy)propan-2-ol is a chiral molecule that features a piperazine ring, a quinoline ring, and a propanol group. Its complex structure and stereochemistry make it a promising candidate for pharmaceutical applications, as it can potentially interact with various biological targets.

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  • 154531-78-9 Structure
  • Basic information

    1. Product Name: (2S)-1-[4-(10,11-dihydro-5H-dibenzo[a,d][7]annulen-5-yl)piperazin-1-yl]-3-(quinolin-5-yloxy)propan-2-ol
    2. Synonyms: 1-Piperazineethanol, 4-(10,11-dihydro-5H-dibenzo(a,d)cyclohepten-5-yl)-alpha-((5-quinolinyloxy)methyl)-, (S)-
    3. CAS NO:154531-78-9
    4. Molecular Formula: C31H33N3O2
    5. Molecular Weight: 479.6126
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 154531-78-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 672.2°C at 760 mmHg
    3. Flash Point: 360.3°C
    4. Appearance: N/A
    5. Density: 1.218g/cm3
    6. Vapor Pressure: 5.52E-19mmHg at 25°C
    7. Refractive Index: 1.653
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: (2S)-1-[4-(10,11-dihydro-5H-dibenzo[a,d][7]annulen-5-yl)piperazin-1-yl]-3-(quinolin-5-yloxy)propan-2-ol(CAS DataBase Reference)
    11. NIST Chemistry Reference: (2S)-1-[4-(10,11-dihydro-5H-dibenzo[a,d][7]annulen-5-yl)piperazin-1-yl]-3-(quinolin-5-yloxy)propan-2-ol(154531-78-9)
    12. EPA Substance Registry System: (2S)-1-[4-(10,11-dihydro-5H-dibenzo[a,d][7]annulen-5-yl)piperazin-1-yl]-3-(quinolin-5-yloxy)propan-2-ol(154531-78-9)
  • 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: 154531-78-9(Hazardous Substances Data)

154531-78-9 Usage

Uses

Used in Pharmaceutical Development:
(2S)-1-[4-(10,11-dihydro-5H-dibenzo[a,d][7]annulen-5-yl)piperazin-1-yl]-3-(quinolin-5-yloxy)propan-2-ol is used as a potential active pharmaceutical ingredient for the development of new medications. Its unique structure allows it to engage with multiple biological targets, making it a versatile compound for treating a range of conditions.
Used in Research and Development:
In the field of scientific research, (2S)-1-[4-(10,11-dihydro-5H-dibenzo[a,d][7]annulen-5-yl)piperazin-1-yl]-3-(quinolin-5-yloxy)propan-2-ol serves as a valuable tool for studying chemical reactions and biological processes. Its complex structure and chirality provide insights into the behavior of molecules in various environments, contributing to a deeper understanding of molecular interactions and mechanisms.

Check Digit Verification of cas no

The CAS Registry Mumber 154531-78-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,5,3 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 154531-78:
(8*1)+(7*5)+(6*4)+(5*5)+(4*3)+(3*1)+(2*7)+(1*8)=129
129 % 10 = 9
So 154531-78-9 is a valid CAS Registry Number.

154531-78-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name CP 162399

1.2 Other means of identification

Product number -
Other names S(-)-5-[3-{4-(dibenzosuberan-5-yl)piperazin-1-yl}-2-hydroxypropoxy]quinoline

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:154531-78-9 SDS

154531-78-9Upstream product

154531-78-9Downstream Products

154531-78-9Relevant articles and documents

Process for production of glycide derivative

-

, (2008/06/13)

A glycide derivative represented by the following general formula (I) is produced by reacting a hydroxyaryl or heteroaryl represented by A-OH with glycidyl tosylate in the presence of a cesium base as a base. Thereby, an aryl glycidyl ether derivative, which is an important intermediate for drug production, can be produced easily and reliably. Particularly when optically active glycidyl tosylate is used, said compound can be obtained at a high optical purity. STR1 wherein A represents an aryl group or a heteroaryl group.

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