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Benzene, 2,5-dimethoxy-1,3-dinitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15174-07-9

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15174-07-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15174-07-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,7 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15174-07:
(7*1)+(6*5)+(5*1)+(4*7)+(3*4)+(2*0)+(1*7)=89
89 % 10 = 9
So 15174-07-9 is a valid CAS Registry Number.

15174-07-9SDS

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 1,4-dimethoxy-2,6-dinitrobenzene

1.2 Other means of identification

Product number -
Other names 1,4-dimethoxy-3,5-dinitrobenzene

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:15174-07-9 SDS

15174-07-9Relevant academic research and scientific papers

A formal synthesis of lavendamycin methyl ester, nitramarine, and their analogues: A povarov approach

Ramesh, Subburethinam,Nagarajan, Rajagopal

, p. 545 - 558 (2013/03/14)

A convergent formal synthesis of lavendamycin methyl ester and synthesis of its analogues have been delineated through the Povarov approach. This protocol is also applied to the formal synthesis of nitramarine (3) in good yield.

Total synthesis of lavendamycin by a [2+2+2] cycloaddition

Nissen, Felix,Detert, Heiner

experimental part, p. 2845 - 2853 (2011/06/26)

The total synthesis of the bacterial-derived, pentacyclic, antitumor antibiotic lavendamycin has been achieved through a highly convergent strategy. The key step of this synthesis is a ruthenium-catalyzed [2+2+2] cycloaddition of an electron-deficient nit

The total synthesis of neoamphimedine

LaBarbera, Daniel V.,Bugni, Tim S.,Ireland, Chris M.

, p. 8501 - 8505 (2008/02/13)

(Chemical Equation Presented) Neoamphimedine, a pyridoacridine alkaloid from Xestospongia sp., is a potent antitumor agent both in vitro and in vivo. Neoamphimedine can efficiently induce topoisomerase II mediated catenation of plasmid DNA in vitro and is

Benzimidazole-4,7-diones as inhibitors of protozoal (Toxoplasma gondii) purine nucleoside phosphorylase

Alvarez, Frédéric,Ghérardi, Arnaud,Nebois, Pascal,Sarciron, Marie-Elizabeth,Pétavy, Anne-Fran?oise,Walchshofer, Nadia

, p. 977 - 979 (2007/10/03)

Benzimidazole-4,7-diones derivatives substituted at 1- and/or 2-position have been synthetized and tested as inhibitors of purine nucleoside phosphorylase (PNP), isolated from two strains of Toxoplasma gondii (RH and ME 49). They were identified as inhibi

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