Welcome to LookChem.com Sign In|Join Free

CAS

  • or

6336-86-3

6-Hydroxytetracene-5,12-dione is a chemical compound with the molecular formula C18H10O3. It is a derivative of tetracene, a polycyclic aromatic hydrocarbon consisting of four fused benzene rings. The compound is characterized by the presence of a hydroxyl group at the 6th carbon position and two carbonyl groups at the 5th and 12th carbon positions. 6-Hydroxytetracene-5,12-dione is known for its potential applications in the synthesis of various organic compounds and materials, such as dyes, pigments, and pharmaceuticals. Due to its unique structure and properties, it has been a subject of interest in chemical research, particularly in the fields of organic synthesis and materials science.

6336-86-3

Post Buying Request

6336-86-3 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

6336-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6336-86-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6336-86:
(6*6)+(5*3)+(4*3)+(3*6)+(2*8)+(1*6)=103
103 % 10 = 3
So 6336-86-3 is a valid CAS Registry Number.

6336-86-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-hydroxytetracene-5,12-dione

1.2 Other means of identification

Product number -
Other names 6-hydroxynaphthacene-5,12-dione

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:6336-86-3 SDS

6336-86-3Relevant articles and documents

THERMAL ADDITION REACTIONS TO BENZOCYCLOBUTENONES STUDIED BY FLASH PHOTOLYSIS

Schiess, P.,Eberle, M.,Huys-Francotte, M.,Wirz, J.

, p. 2201 - 2204 (2007/10/02)

Ortho-quinoid vinylketenes 2 have been generated thruogh flash photolysis of benzocyclobutenones 1.A kinetic study of intermolecular addition reactions of 2 competing with the recyclization 2 -> 1 reveals strikingly different substituent effects for the addition of methanol and of dienophiles.

SYNTHESIS AND STRUCTURE OF COMPOUNDS OBTAINED DURING ACYLATION OF 6-PHENYLAMINO-5,11-NAPHTHACENEQUINONE

Gerasimenko, Yu. E.,Poteleshchenko, N. T.,Romanov, V. V.

, p. 1646 - 1650 (2007/10/02)

N,O-Acylotropic tautomerism was found in N-acetyl and N-benzoyl-6-phenylamino-5,11-naphthacenequinones, obtained by acylation of 6-phenylamino-5,11-naphthacenequinone with acetic and benzoic anhydrides in the presence of sulfuric acid.The reaction of 6-phenylamino-5,11-naphthacenequinone with acetic anhydride in pyridine does not stop at the N-acetylation stage, but addition occurs at position 12 of the carbanion generated from acetic acid in the presence of pyridine by a reaction of the Michael type with subsequent oxidation of the dihydro derivative and closure of the pyrone ring.A new heterocyclic derivative of naphtacene, i.e., N-acetyl-9-phenylaminonaphthacenopyran-2,8-dione, was obtained.

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 6336-86-3