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2,5-bis(aziridin-1-yl)-3-fluoro-6-(morpholin-4-yl)cyclohexa-2,5-diene-1,4-dione is a complex chemical compound characterized by its multiple functional groups. It features two aziridine groups, which are heterocyclic organic compounds with a three-membered ring structure consisting of two carbon atoms and one nitrogen atom. Additionally, it incorporates a fluoro group and a morpholine group, both of which are prevalent in pharmaceuticals and agrochemicals. The cyclohexa-2,5-diene-1,4-dione core of the molecule contributes to its high reactivity, making it a promising candidate for use as a building block in the synthesis of other complex organic compounds.

59886-45-2

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59886-45-2 Usage

Uses

Used in Pharmaceutical Industry:
2,5-bis(aziridin-1-yl)-3-fluoro-6-(morpholin-4-yl)cyclohexa-2,5-diene-1,4-dione is used as a potential active pharmaceutical ingredient (API) for its diverse functional groups, which may contribute to its medicinal properties. The presence of aziridine, fluoro, and morpholine groups suggests that 2,5-bis(aziridin-1-yl)-3-fluoro-6-(morpholin-4-yl)cyclohexa-2,5-diene-1,4-dione could be involved in the development of new drugs, particularly in areas where its reactivity and structural features can be exploited for therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 2,5-bis(aziridin-1-yl)-3-fluoro-6-(morpholin-4-yl)cyclohexa-2,5-diene-1,4-dione is used as a potential component in the development of new pesticides or herbicides. 2,5-bis(aziridin-1-yl)-3-fluoro-6-(morpholin-4-yl)cyclohexa-2,5-diene-1,4-dione's structural complexity and functional groups may offer unique modes of action, potentially leading to the creation of novel agrochemical products that can address resistance issues or provide new solutions for crop protection.
Used in Organic Synthesis:
2,5-bis(aziridin-1-yl)-3-fluoro-6-(morpholin-4-yl)cyclohexa-2,5-diene-1,4-dione is used as a synthetic intermediate or building block in the preparation of other complex organic compounds. Its reactivity and the presence of various functional groups make it a valuable starting material for the synthesis of a wide range of chemical products, including specialty chemicals, advanced materials, and potentially new pharmaceuticals or agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 59886-45-2 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 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 59886-45:
(7*5)+(6*9)+(5*8)+(4*8)+(3*6)+(2*4)+(1*5)=192
192 % 10 = 2
So 59886-45-2 is a valid CAS Registry Number.

59886-45-2SDS

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 2,5-bis(aziridin-1-yl)-3-fluoro-6-morpholin-4-ylcyclohexa-2,5-diene-1,4-dione

1.2 Other means of identification

Product number -
Other names 2,4-dione,2,5-bis(1-aziridinyl)-3-fluoro-6-(4-morpholinyl)

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:59886-45-2 SDS

59886-45-2Downstream Products

59886-45-2Relevant academic research and scientific papers

Potential central nervous system antitumor agents. Aziridinylbenzoquinones. 2

Chou,Khan,Driscoll

, p. 1302 - 1308 (2007/10/09)

A series of 15 2,5 diaziridinyl 3,6 bis(alkylamino) 1,4 benzoquinone derivatives was synthesized and evaluated as central nervous system antitumor agents in the murine intracerebral L1210 and ependymoblastoma brain tumor systems. Intraperitoneal activity was evaluated in the leukemia L1210, P388, and B16 melanocarcinoma tumor models. The more hydrophilic hydroxyalkylamino compounds were the most effective in the intraperitoneal ascites systems (L1210, P388) with the dihydroxypropylamino and hydroxyethylamino analogues producing long term survivors. The simple, more lipophilic mono and dialkylamino derivatives were most effective in the intracerebral systems. Multiple long term survivors were obtained with the methyl, ethyl, and dimethylamino compounds in the ependymoblastoma brain tumor system. The parent amino analogue was very active in several tumor models. The relationships between structure, activity, and water solubility are discussed.

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