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78808-07-8

The chemical "9-{[4-(4-chlorophenyl)piperazin-1-yl]methyl}-4-methyl-8,9-dihydro-2H,10H-pyrano[2,3-f]chromene-2,10-dione" is a complex organic compound with a molecular formula of C26H23ClN2O3. It features a pyrano[2,3-f]chromene core structure, which is a type of fused heterocyclic compound. The molecule contains a 4-methyl group attached to the pyrano[2,3-f]chromene ring, and a 9-{[4-(4-chlorophenyl)piperazin-1-yl]methyl} substituent, which adds complexity to its structure. 9-{[4-(4-chlorophenyl)piperazin-1-yl]methyl}-4-methyl-8,9-dihydro-2H,10H-pyrano[2,3-f]chromene-2,10-dione is characterized by the presence of a 4-chlorophenyl group within the piperazine ring, contributing to its overall chemical properties. It is a white to off-white crystalline solid and is known for its potential applications in the pharmaceutical industry, particularly as a serotonin receptor agonist. The compound's structure and properties make it a subject of interest for researchers in the field of medicinal chemistry.

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  • 78808-07-8 Structure

  • Basic information

    1. Product Name: 9-{[4-(4-chlorophenyl)piperazin-1-yl]methyl}-4-methyl-8,9-dihydro-2H,10H-pyrano[2,3-f]chromene-2,10-dione
    2. Synonyms: 2H,10H-Benzo(1,2-b:3,4-b')dipyran-2,10-dione, 8,9-dihydro-9-((4-(4-chlorophenyl)-1-piperazinyl)methyl)-4-methyl-
    3. CAS NO:78808-07-8
    4. Molecular Formula: C24H23ClN2O4
    5. Molecular Weight: 438.9034
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 78808-07-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 645.7°C at 760 mmHg
    3. Flash Point: 344.3°C
    4. Appearance: N/A
    5. Density: 1.338g/cm3
    6. Vapor Pressure: 1.47E-16mmHg at 25°C
    7. Refractive Index: 1.625
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 9-{[4-(4-chlorophenyl)piperazin-1-yl]methyl}-4-methyl-8,9-dihydro-2H,10H-pyrano[2,3-f]chromene-2,10-dione(CAS DataBase Reference)
    11. NIST Chemistry Reference: 9-{[4-(4-chlorophenyl)piperazin-1-yl]methyl}-4-methyl-8,9-dihydro-2H,10H-pyrano[2,3-f]chromene-2,10-dione(78808-07-8)
    12. EPA Substance Registry System: 9-{[4-(4-chlorophenyl)piperazin-1-yl]methyl}-4-methyl-8,9-dihydro-2H,10H-pyrano[2,3-f]chromene-2,10-dione(78808-07-8)

  • 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: 78808-07-8(Hazardous Substances Data)

78808-07-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78808-07-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,0 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78808-07:
(7*7)+(6*8)+(5*8)+(4*0)+(3*8)+(2*0)+(1*7)=168
168 % 10 = 8
So 78808-07-8 is a valid CAS Registry Number.

78808-07-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-[[4-(4-chlorophenyl)piperazin-1-yl]methyl]-4-methyl-8,9-dihydropyrano[2,3-f]chromene-2,10-dione

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:78808-07-8 SDS

78808-07-8Downstream Products

78808-07-8Relevant articles and documents

Novel Mannich Reaction of 8-Acetyl-7-hydroxy-4-methylcoumarin with 1-Arylpiperazines

Samant, S. D.,Deodhar, K. D.,Kulkarni, R. A.

, p. 215 - 217 (2007/10/02)

8-Acetyl-7-hydroxy-4-methylcoumarin (I) reacts with 1-arylpiperazines in the presence of excess paraformaldehyde to yield 4-methyl-9-(4-aryl-1-piperazinylmethyl)-2H,10H-8,9-dihydrobenzodipyran-2,10-diones, instead of the Mannich bases (II) or (III).The compounds show action on smooth muscles and act as agonists to the heart muscle receptors.

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