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78493-48-8

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78493-48-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78493-48-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,4,9 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78493-48:
(7*7)+(6*8)+(5*4)+(4*9)+(3*3)+(2*4)+(1*8)=178
178 % 10 = 8
So 78493-48-8 is a valid CAS Registry Number.

78493-48-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name leuconile blue A

1.2 Other means of identification

Product number -
Other names 5-AMINO-9-(DIETHYLAMINO)-12H-BENZO[A]PHENOXAZINE

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:78493-48-8 SDS

78493-48-8Upstream product

78493-48-8Downstream Products

78493-48-8Relevant articles and documents

Novel synthetic route for antimalarial benzo[a]phenoxazine derivative SSJ-183 and two active metabolites

Mizukawa, Yuki,Ge, Jian-Feng,Bakar Md, Abu,Itoh, Isamu,Scheurer, Christian,Wittlin, Sergio,Brun, Reto,Matsuoka, Hiroyuki,Ihara, Masataka

, p. 3749 - 3752 (2014)

A productive synthesis of benzo[a]phenoxazine derivative SSJ-183 (1), a promising lead for antimalarial agents, was developed using a one pot procedure. Furthermore, N-deethylated metabolite 3 and bis-N,N-deethylated metabolite 4 were synthesized by the application of the method. The metabolites 3 and 4 showed comparable and ~2-fold increased activities against drug-sensitive and drug-resistant Plasmodium falciparum parasites.

Photoelectrochemistry in Colloidal Systems. Part 2. - A Photogalvanic Cell Based on TiO2 Semiconductor Colloid

Kamat, Prashant V.

, p. 509 - 518 (2007/10/02)

Thiazine and oxazine dyes have been photoelectrochemically reduced in colloidal TiO2 suspensions with bandgap excitation.The one-electron reduction of the dye, which resulted in the production of the semireduced radical ion, with quantum yield up to 0.1, further disproportionated to yield a stable leuco dye.The efficiency of the interfacial electron-transfer process is found to be dependent on the standard reduction potential of the dye.The feasibility of employing a colloidal semiconductor system in the operation of a photogalvanic cell is demonstrated.A photogalvanic power conversion efficiency of 0.002percent was achieved with thionine and colloidal TiO2 upon bandgap excitation.The use of TiO2 colloid as a carrier for the deposition of a photoactive or an electroactive species on the electrode surface is also discussed.

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