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1,6-DINITROPHENAZINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36848-41-6

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36848-41-6 Usage

Appearance

Pale yellow crystalline solid

Uses

a. Production of dyes
b. Production of pharmaceuticals
c. Intermediate in organic synthesis

Classification

Nitroaromatic compound

Hazard

Highly explosive, hazardous material

Synthesis

Nitration of phenazine with concentrated nitric acid and sulfuric acid

Main applications

a. Dye intermediate
b. Precursor to various pharmaceuticals

Handling and storage

Carefully handled, stored in tightly sealed containers

Check Digit Verification of cas no

The CAS Registry Mumber 36848-41-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,8,4 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 36848-41:
(7*3)+(6*6)+(5*8)+(4*4)+(3*8)+(2*4)+(1*1)=146
146 % 10 = 6
So 36848-41-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H6N4O4/c17-15(18)9-5-1-3-7-11(9)14-8-4-2-6-10(16(19)20)12(8)13-7/h1-6H

36848-41-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6-dinitrophenazine

1.2 Other means of identification

Product number -
Other names BZGCNHUWISZVPK-UHFFFAOYSA

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:36848-41-6 SDS

36848-41-6Upstream product

36848-41-6Relevant academic research and scientific papers

Synthesis of phenazine derivatives for use as precursors to electrochemically generated bases

Mateo Alonso,Horcajada, Roberto,Groombridge, Helen J.,Chudasama, Reshma,Motevalli, Majid,Utley, James H. P.,Wyatt, Peter B.

, p. 2832 - 2841 (2007/10/03)

1,6-Disubstituted phenazine derivatives for use as precursors to electrochemically generated bases have been synthesized from readily available starting materials. Reaction of 1,6-dihydroxyphenazine with 1,10-diododecane, 1,1 1-diiodo-3,6,9-trioxaundecane

Synthesis of novel acridino- and phenazino-18-crown-6 ligands and their optically pure dimethyl-substituted analogues for molecular recognition studies

Huszthy, Peter,Samu, Erika,Vermes, Borbala,Mezey-Vandor, Gabriella,Nogradi, Mihaly,Bradshaw, Jerald S.,Izatt, Reed M.

, p. 1491 - 1504 (2007/10/03)

Novel acridino- and phenazino-18-crown-6 ligands 5 and 6 were prepared from acridine-4.5-diol (9) and phenazine-1,9-diol (10) with tetraethylene glycol di-p-tosylate (11) using potassium tert-butoxide as a base in THF. New optically pure dimethyl-substitu

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