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

61973-25-9

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61973-25-9 Usage

Structure

Bicyclic compound with a dithioether and lactam structure

Molecular weight

295.46 g/mol

Common uses

Organic synthesis, pharmaceutical research for drug development

Applications

Medicinal chemistry, drug discovery

Potential biological activities

Requires further investigation.

Check Digit Verification of cas no

The CAS Registry Mumber 61973-25-9 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 61973-25:
(7*6)+(6*1)+(5*9)+(4*7)+(3*3)+(2*2)+(1*5)=139
139 % 10 = 9
So 61973-25-9 is a valid CAS Registry Number.

61973-25-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names (1R,4R)-1-Benzyl-4,5,7-trimethyl-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:61973-25-9 SDS

61973-25-9Downstream Products

61973-25-9Relevant academic research and scientific papers

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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