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2,3-Dithia-5,7-diazabicyclo[2.2.2]octane-6,8-dione, 5,7-dimethyl-1,4-bis(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61973-22-6

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61973-22-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61973-22-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,7 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61973-22:
(7*6)+(6*1)+(5*9)+(4*7)+(3*3)+(2*2)+(1*2)=136
136 % 10 = 6
So 61973-22-6 is a valid CAS Registry Number.

61973-22-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dibenzyl-5,7-dimethyl-2,3-dithia-5,7-diaza-bicyclo[2.2.2]octane-6,8-dione

1.2 Other means of identification

Product number -
Other names (1S,4S)-1,4-Dibenzyl-5,7-dimethyl-2,3-dithia-5,7-diaza-bicyclo[2.2.2]octane-6,8-dione

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:61973-22-6 SDS

61973-22-6Downstream Products

61973-22-6Relevant academic research and scientific papers

Synthesis and biological evaluation of epidithio-, epitetrathio-, and bis-(methylthio)diketopiperazines: Synthetic methodology, enantioselective total synthesis of epicoccin G, 8,8′-epi-ent-rostratin B, gliotoxin, gliotoxin G, emethallicin E, and haematocin and discovery of new antiviral and antimalarial agents

Nicolaou, K. C.,Lu, Min,Totokotsopoulos, Sotirios,Heretsch, Philipp,Giguere, Denis,Sun, Ya-Ping,Sarlah, David,Nguyen, Thu H.,Wolf, Ian C.,Smee, Donald F.,Day, Craig W.,Bopp, Selina,Winzeler, Elizabeth A.

supporting information, p. 17320 - 17332,13 (2020/09/02)

An improved sulfenylation method for the preparation of epidithio-, epitetrathio-, and bis-(methylthio)diketopiperazines from diketopiperazines has been developed. Employing NaHMDS and related bases and elemental sulfur or bis[bis(trimethylsilyl)amino]trisulfide (23) in THF, the developed method was applied to the synthesis of a series of natural and designed molecules, including epicoccin G (1), 8,8′-epi-ent-rostratin B (2), gliotoxin (3), gliotoxin G (4), emethallicin E (5), and haematocin (6). Biological screening of selected synthesized compounds led to the discovery of a number of nanomolar antipoliovirus agents (i.e., 46, 2,2′-epi-46, and 61) and several low-micromolar anti-Plasmodium falciparum lead compounds (i.e., 46, 2,2′-epi-46, 58, 61, and 1).

A practical sulfenylation of 2,5-diketopiperazines

Nicolaou,Giguere, Denis,Totokotsopoulos, Sotirios,Sun, Ya-Ping

supporting information; experimental part, p. 728 - 732 (2012/03/08)

Sulfurs in action: A practical and simple method has been developed for the introduction of sulfur atoms into 2,5-diketopiperazines (I) under mild conditions. The reaction provides more or less complex epidithiodiketopiperazines (II) and bis-methylthiodik

TOTAL SYNTHESIS OF GLIOTOXIN, DEHYDROGLIOTOXIN AND HYALODENDRIN

Fukuyama, Tohru,Nakatsuka, Shin-Ichi,Kishi, Yoshito

, p. 2045 - 2078 (2007/10/02)

Two general methods, Method A and Method B in Scheme 19, to synthesize epidithiapiperazinediones, are described.A total synthesis of racemic and optically active gliotoxin (1) and of racemic dehydrogliotoxin (53) was achieved by using Method A, whereas a total synthesis of racemic hyalodendrin (52) was completed by using Method B.

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