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52864-94-5

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52864-94-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52864-94-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,6 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 52864-94:
(7*5)+(6*2)+(5*8)+(4*6)+(3*4)+(2*9)+(1*4)=145
145 % 10 = 5
So 52864-94-5 is a valid CAS Registry Number.

52864-94-5SDS

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 2,3-bis(phenylsulfanyl)naphthalene-1,4-dione

1.2 Other means of identification

Product number -
Other names 1,4-Naphthalenedione,2,3-bis(phenylthio)

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:52864-94-5 SDS

52864-94-5Downstream Products

52864-94-5Relevant articles and documents

Synthesis and?evaluation of?antifungal activity of?naphthoquinone derivatives

Errante, Giaccomo,La Motta, Grazia,Lagana, Catarina,Wittebolle, Vierle,Sarciron, Marie-élisabeth,Barret, Roland

, p. 773 - 778 (2006)

3-Arylamino-2-phenylsulfinylnaphthoquinones, 2,3-diarylthio-naphthoquinones and 2-phenylsulfinyl-3-arylthio-1,4-dihydronaphtalenes are synthesized and tested against five fungi. The activities of these products were better than amphotericine B against all

Reaction of 2,3-bis(benzotriazol-1-y1)-1,4-naphthoquinone

Romanyuk,Litvin,Ganushchak

, p. 655 - 656 (2001)

-

NAPHTHAQUINONE METHYLTRANSFERASE INHIBITORS AND USES THEREOF

-

Page/Page column 87; 89, (2015/11/27)

Provided herein are compounds of (I), and pharmaceutically acceptable salts, solvates, hydrates, polymorphs, co-crystals, tautomers, stereoisomers, and prodrugs thereof. Also provided are pharmaceutical compositions and methods involving the inventive compounds for the treatment of proliferative diseases (e.g., cancer (e.g., leukemia, breast cancer, melanoma, metastatic cancer) and diseases associated with inappropriate SET8 activity. Also provided are methods for inhibiting SET8 and methods for labelling SET8.

Synthesis and selective anticancer activity of organochalcogen based redox catalysts

Doering, Mandy,Ba, Lalla A.,Lilienthal, Nils,Nicco, Carole,Scherer, Christiane,Abbas, Muhammad,Zada, Abdul Ali Peer,Coriat, Romain,Burkholz, Torsten,Wessjohann, Ludger,Diederich, Marc,Batteux, Frederic,Herling, Marco,Jacob, Claus

supporting information; experimental part, p. 6954 - 6963 (2010/12/25)

Many tumor cells exhibit a disturbed intracellular redox state resulting in higher levels of reactive oxygen species (ROS). As these contribute to tumor initiation and sustenance, catalytic redox agents combining significant activity with substrate specif

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