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CAS

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17798-09-3

fluoranthen-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 17798-09-3 Structure

  • Basic information

    1. Product Name: fluoranthen-3-ol
    2. Synonyms: 3-fluoranthenol
    3. CAS NO:17798-09-3
    4. Molecular Formula: C16H10O
    5. Molecular Weight: 218.25
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17798-09-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 437.4°C at 760 mmHg
    3. Flash Point: 213°C
    4. Appearance: N/A
    5. Density: 1.36g/cm3
    6. Vapor Pressure: 2.92E-08mmHg at 25°C
    7. Refractive Index: 1.895
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: fluoranthen-3-ol(CAS DataBase Reference)
    11. NIST Chemistry Reference: fluoranthen-3-ol(17798-09-3)
    12. EPA Substance Registry System: fluoranthen-3-ol(17798-09-3)

  • 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: 17798-09-3(Hazardous Substances Data)

17798-09-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17798-09-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,7,9 and 8 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17798-09:
(7*1)+(6*7)+(5*7)+(4*9)+(3*8)+(2*0)+(1*9)=153
153 % 10 = 3
So 17798-09-3 is a valid CAS Registry Number.

17798-09-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name fluoranthen-3-ol

1.2 Other means of identification

Product number -
Other names 3-hydroxyfluoranthene

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:17798-09-3 SDS

17798-09-3Relevant articles and documents

C–H Acyloxylation of Polycyclic Aromatic Hydrocarbons

Itami, Kenichiro,Murakami, Kei,Sakakibara, Yota

supporting information, p. 602 - 607 (2022/01/28)

The C–H acyloxylation of polycyclic aromatic hydrocarbons (PAHs) is described. This reaction constructs aryl acyloxylate scaffolds from PAHs with equimolar hypervalent iodine compounds under mild reaction conditions. Interestingly, the blue light irradiat

Reactions of Spiro-indazoles containing Keto-groups. Syntheses of Benzaceanthrylenes, Naphthaceanthrylenes, and Fluoranthenes

Hirakawa, Kioyoichi,Toki, Takuya,Yamazaki, Kazuo,Nakazawa, Sho

, p. 1944 - 1949 (2007/10/02)

Anthrone-10-spiro-3'-3'H-imidazole (1) and 3H-indazole-3-spiro-1'-naphthalen-4'(1'H)-one (3), prepared by the cycloaddition of benzyne with 10-diazoanthrone (6) and 4-diazanaphthalen-1(4H)-one (7), respectively, thermally rearranged with elimination of nitrogen to 8-hydroxybenzaceanthrylene (9b) and 3-hydroxyfluoranthene (11b), respectively.The diazoketone (6) reacted with 1,2-naphthyne to give anthrone-10-spiro-3'-3'H-benzindazole (4) and anthrone-10-spiro-1'-1'H-benzindazole (5), which gave the rearrangement product, 10-hydroxynaphthaceanthrylene (12b) by thermolysis.Photolysis of the spiro-indazoles afforded the rearrangement and/or photo-oxidation products.Thermolysis and photolysis are accountable on the basis of formation of biradicals and isomerization of these to fused polycyclic compounds.In particular, the isomerization of the biradical (21) to (12b) involves the formation of the naphthocyclopropene (20).

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