Welcome to LookChem.com Sign In|Join Free

CAS

  • or

7132-70-9

Acridin-3-ol, also known as 3-hydroxyacridine, is a heterocyclic aromatic compound with the chemical formula C13H9NO. It is a white crystalline solid that is soluble in organic solvents and has a melting point of 156-160°C. Acridin-3-ol is a derivative of acridine, a tricyclic compound with a central nitrogen atom, and is often used as a building block in the synthesis of various acridine-based compounds. These compounds have diverse applications, including as fluorescent dyes, chemiluminescent agents, and potential therapeutic agents in the development of anti-cancer and anti-bacterial drugs. Acridin-3-ol's chemical properties and reactivity make it a valuable intermediate in organic synthesis and a subject of interest in medicinal chemistry research.

7132-70-9 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 7132-70-9 Structure

  • Basic information

    1. Product Name: Acridin-3-ol
    2. Synonyms: Acridin-3-ol
    3. CAS NO:7132-70-9
    4. Molecular Formula: C13H9NO
    5. Molecular Weight: 195.2167
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 7132-70-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 458.5°Cat760mmHg
    3. Flash Point: 209.1°C
    4. Appearance: /
    5. Density: 1.28g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.768
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: Acridin-3-ol(CAS DataBase Reference)
    11. NIST Chemistry Reference: Acridin-3-ol(7132-70-9)
    12. EPA Substance Registry System: Acridin-3-ol(7132-70-9)

  • 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: 7132-70-9(Hazardous Substances Data)

7132-70-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7132-70-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,3 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7132-70:
(6*7)+(5*1)+(4*3)+(3*2)+(2*7)+(1*0)=79
79 % 10 = 9
So 7132-70-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H9NO/c15-11-6-5-10-7-9-3-1-2-4-12(9)14-13(10)8-11/h1-8,15H

7132-70-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 10H-acridin-3-one

1.2 Other means of identification

Product number -
Other names 3-Acridinol

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:7132-70-9 SDS

7132-70-9Downstream Products

7132-70-9Relevant articles and documents

The behavior of 2-chloroquinoline-3-carbaldehyde and 2-oxoquinoline-3-carbaldehyde toward stabilized methylenetriphenylphosphoranes and secondary amines

El-Samahy, Fatma A.,Ibrahim, Nabila M.,Mahran, Mohamed R.H.

, p. 59 - 64 (2016)

In this study use was made of the Wittig carbonyl olefination reaction and stereo-identification of the resulting alkenes. Condensation of 2-chloroquinoline-3-carbaldehyde with some selected stabilized phosphonium ylides yielded a mixture of the corresponding E and Z olefins in each case. On the other hand reaction of 2-oxoquinoline-3-carbaldehyde with the selected ylides afforded the respective olefins only in one of the possible stereoisomers. The reaction of 2-chloroquinoline-3-carbaldehyde with acetylmethylenetriphenylphosphorane produced the respective olefine together with acridin-3-ol. Heating of (E) and/or (Z)-methyl 3-(2-chloroquinolin-3-yl)acrylate with hydrazine hydrate yielded the corresponding propan-1-ol derivative. Dechlorination of (E)-ethyl 3-(2-chloroquinolin-3-yl)acrylate and/or (E)-4-(2-chloroquinolin-3-yl)but-3-en-2-one was effected upon treatment with morpholine or piperidine in absolute ethanol to give the respective enone derivatives.

Inter- and Intramolecular Chiral Stacking of Acridine Derivatives

Jodal, Ildiko,Kovacs, Antal,Ott, Juergen,Snatzke, Guenther

, p. 1207 - 1210 (2007/10/02)

Sugar derivatives of diaminoacridine stack in aqueous solution like the parent compound.This is shown by CD measurements which give concentration-depending CD couplets.An extraordinarily strong CD couplet is obtained around 255 nm when two units of hydroxyacridine (base changed for solubility reasons) are connected by a 6-membered chain. - Key Words: Circular dichroism, dependence on concentration / Exciton interaction

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 7132-70-9