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1785-52-0

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1785-52-0 Usage

Uses

6,11-Dihydroxy-5,12-naphthacenedione was used in the synthesis of a tetracene derivative, 5,6,11,12-tetrachlorotetracene. It was also used for the synthesis of (3Z,3′Z)-3,3′-(ethane-1,2-diylidene)bis[isobenzofuran-1(3H)-one]. It may be used for the following studies:Synthesis of self-assembled, chair-shaped dirhenium(I) macrocyclic compounds.Synthesis of half-sandwich Ir, Rh-based organometallic molecular boxes.As ligand for the synthesis of supramolecular coordination complexes (SCCs).

General Description

Crystallographic analysis of 6,11-dihydroxy-5,12-naphthacenedione has been reported. Study indicates the presence of (3Z,3′Z)-3,3′-(ethane-1,2-diylidene)bis[isobenzofuran-1(3H)-one] as impurity.

Check Digit Verification of cas no

The CAS Registry Mumber 1785-52-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,8 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1785-52:
(6*1)+(5*7)+(4*8)+(3*5)+(2*5)+(1*2)=100
100 % 10 = 0
So 1785-52-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H10O4/c19-15-9-5-1-2-6-10(9)16(20)14-13(15)17(21)11-7-3-4-8-12(11)18(14)22/h1-8,19-20H

1785-52-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,11-dihydroxytetracene-5,12-dione

1.2 Other means of identification

Product number -
Other names 5,12-dihydroxy-6,13-tetracenequinone

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:1785-52-0 SDS

1785-52-0Relevant articles and documents

Synthesis, Rearrangement, and Hauser Annulation of 3-Isocyanophthalides

Mal, Dipakranjan,Ghosh, Ketaki,Chakraborty, Soumen

, p. 2473 - 2484 (2015/08/18)

3-Isocyanoisobenzofuran-1(3H)-ones (phthalides) were prepared in two steps from the corresponding phthalaldehydic acids. The 3-isocyanoisobenzofuran-1(3H)-ones are readily rearranged to the corresponding 3-cyanoisobenzofuran-1(3H)-ones using triflic anhyd

Direct access to 1,4-dihydroxyanthraquinones: The Hauser annulation reexamined with p-quinones

Mal, Dipakranjan,Ray, Sutapa,Sharma, Indrajeet

, p. 4981 - 4984 (2008/02/05)

(Chemical Equation Presented) 3-Phenylsulfanylphthalides (e.g. 8a) readily react with p-benzoquinones in the presence of LiOtBu in THF to furnish 1,4-dihydroxyanthraquinones in good yields and one-pot operations.

METAL TEMPLATE ORTHO-ACYLATION OF PHENOLS; A NEW GENERAL APPROACH TO ANTHRACYCLINONES

Sartori, Giovanni,Casnati, Giuseppe,Bigi, Franca,Robles, Pasquale

, p. 1533 - 1536 (2007/10/02)

Direct and mild synthesis of dihydroxyanthraquinones including 4-demethoxy-7-deoxydaunomycinone 8 from ortho-phthaloyl dichloride and hydroquinone derivatives is described.

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