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1,2-epoxy-3,4-dihydroxy-1,2,3,4-tetrahydrobenzo(c)phenanthrene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 111001-48-0 Structure
  • Basic information

    1. Product Name: 1,2-epoxy-3,4-dihydroxy-1,2,3,4-tetrahydrobenzo(c)phenanthrene
    2. Synonyms: 1,2-epoxy-3,4-dihydroxy-1,2,3,4-tetrahydrobenzo(c)phenanthrene
    3. CAS NO:111001-48-0
    4. Molecular Formula: C18H14O3
    5. Molecular Weight: 278.302
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 111001-48-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 567.5°Cat760mmHg
    3. Flash Point: 297°C
    4. Appearance: /
    5. Density: 1.478g/cm3
    6. Vapor Pressure: 1.03E-13mmHg at 25°C
    7. Refractive Index: 1.814
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 1,2-epoxy-3,4-dihydroxy-1,2,3,4-tetrahydrobenzo(c)phenanthrene(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1,2-epoxy-3,4-dihydroxy-1,2,3,4-tetrahydrobenzo(c)phenanthrene(111001-48-0)
    12. EPA Substance Registry System: 1,2-epoxy-3,4-dihydroxy-1,2,3,4-tetrahydrobenzo(c)phenanthrene(111001-48-0)
  • 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: 111001-48-0(Hazardous Substances Data)

111001-48-0 Usage

Type of Compound

Polycyclic aromatic hydrocarbon (PAH)

Potent mutagen

It can cause changes in the DNA sequence, leading to mutations.

Carcinogenic

It has the potential to cause cancer in living organisms.

Formation

Result of the reaction between a benzo(c)phenanthrene diol and an epoxide group.

Presence

Commonly found in cigarette smoke and other sources of combustion.

DNA damage

Can cause damage to the DNA structure, potentially leading to mutations.

Cell transformation

Can induce changes in cell behavior, potentially contributing to the development of cancer.

Implicated in lung cancer

Associated with an increased risk of developing lung cancer.

Respiratory diseases

Linked to the development of other respiratory diseases due to its presence in combustion sources.

Risk Reduction

Minimizing exposure to 1,2-epoxy-3,4-dihydroxy-1,2,3,4-tetrahydrobenzo(c)phenanthrene can help reduce the risk of adverse health effects, including cancer and respiratory diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 111001-48-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,0,0 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 111001-48:
(8*1)+(7*1)+(6*1)+(5*0)+(4*0)+(3*1)+(2*4)+(1*8)=40
40 % 10 = 0
So 111001-48-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H14O3/c19-15-12-8-7-10-6-5-9-3-1-2-4-11(9)13(10)14(12)17-18(21-17)16(15)20/h1-8,15-20H

111001-48-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1a,2,3,11d-Tetrahydrobenzo[5,6]phenanthro[3,4-b]oxirene-2,3-diol

1.2 Other means of identification

Product number -
Other names rac-3-propylisochroman-1-one

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:111001-48-0 SDS

111001-48-0Relevant articles and documents

An Efficient Synthesis of the Highly Tumorigenic anti-Diol Epoxide Derivative of Benzophenanthrene

Pataki, John,Raddo, Pasquale Di,Harvey, Ronald G.

, p. 840 - 844 (2007/10/02)

Synthesis of the potent tumorigen trans-3,4-dihydroxy-anti-1,2,3,4-tetrahydrobenzophenanthrene (1) in relatively few steps and superior overall yield is described.The method entails synthesis of the key intermediate 3-hydroxybenzophenanthrene (7b) v

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