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667-92-5

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667-92-5 Usage

Usage

Antimalarial and antipneumocystic medication

Mechanism of Action

Disrupts the electron transport chain in the mitochondria of Plasmodium and Pneumocystis organisms

Applications

Used in combination with proguanil for malaria prevention and treatment
Stand-alone medication for prevention and treatment of Pneumocystis pneumonia in HIV/AIDS patients

Dosage Forms

Tablets
Suspension

Safety Profile

Generally well-tolerated
Few adverse effects

Check Digit Verification of cas no

The CAS Registry Mumber 667-92-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,6 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 667-92:
(5*6)+(4*6)+(3*7)+(2*9)+(1*2)=95
95 % 10 = 5
So 667-92-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H10Cl2O4/c1-5-3-7(17)10-8(18)4-6(2)12(19)11(10)9(5)13(20)14(15)16/h3-4,14,17H,1-2H3

667-92-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-(2,2-dichloroacetyl)-5-hydroxy-2,7-dimethylnaphthalene-1,4-dione

1.2 Other means of identification

Product number -
Other names 8-Dichloracetyl-5-methoxy-2,7-dimethyl-naphthochinon-1,4

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:667-92-5 SDS

667-92-5Downstream Products

667-92-5Relevant articles and documents

Total synthesis of the antifungal natural product mollisin

Schwolow, Sonja,Kunz, Horst,Rheinheimer, Joachim,Opatz, Till

, p. 6519 - 6524 (2013/11/06)

Mollisin, a bioactive polyketide secondary metabolite of the fungus Mollisia caesia, was synthesized in nine linear steps from commercially available 2,6-dimethyl-γ-pyrone. A key transformation in this first total synthesis of mollisin was the ipso substi

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