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59888-49-2

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59888-49-2 Usage

General Description

2,3,10,10-tetramethyl-2,3-dihydro-10H-3,10a-epidithiopyrazino[1,2-a]indole-1,4-dione is a chemical compound with a complex structure. It is a dithiopyrazinoindole derivative with four methyl groups attached to it. 2,3,10,10-tetramethyl-2,3-dihydro-10H-3,10a-epidithiopyrazino[1,2-a]indole-1,4-dione has potential biological activities and may have applications in medicinal chemistry and pharmaceutical research. However, more research is needed to fully understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 59888-49-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,8 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 59888-49:
(7*5)+(6*9)+(5*8)+(4*8)+(3*8)+(2*4)+(1*9)=202
202 % 10 = 2
So 59888-49-2 is a valid CAS Registry Number.

59888-49-2SDS

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 (3R)-2,3,10,10-tetramethyl-2,3-dihydro-10H-3r,10ac-epidisulfano-pyrazino[1,2-a]indole-1,4-dione

1.2 Other means of identification

Product number -
Other names -

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

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More Details:59888-49-2 SDS

59888-49-2Downstream Products

59888-49-2Relevant articles and documents

Gliotoxin analogues as inhibitors of reverse transcriptase. 1. Effect of lipophilicity.

Ottenheijm,H.C.J. et al.

, p. 796 - 799 (2007/10/08)

The reaction scheme, developed for the synthesis of the gliotoxin analogue 2, was found to be of general applicability for analogues with varying substituents at N(1) and C(2). Analogues 11b-g prepared by this method are inhibitors of reverse transcriptase (RNA-directed DNA polymerase). Their inhibitory activity seems to be related to the lipophilicity of the effector molecules: the most lipophilic compound is the most active inhibitor. The techniques of reversed-phase thin-layer chromatography with silylated, precoated plates as well as reversed-phase high-performance liquid chromatography were used to measure the relative lipophilicities; both techniques gave analogous results.

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