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1,2,4,5-tetrazinane-3,6-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

624-40-8

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624-40-8 Usage

Usage

Medication for the treatment of certain types of brain cancer, including glioblastoma multiforme

Mechanism of Action

Alters the DNA in cancer cells, leading to their death

Classification

Antimetabolite

Mimics

Normal chemicals in the cell

Administration

Typically administered orally in the form of capsules

Absorption

Well-absorbed into the bloodstream

Common Side Effects

Nausea, vomiting, and low blood cell counts

Risk

May increase the risk of developing certain types of leukemia

Importance

Widely used medication in the treatment of brain cancer

Check Digit Verification of cas no

The CAS Registry Mumber 624-40-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 624-40:
(5*6)+(4*2)+(3*4)+(2*4)+(1*0)=58
58 % 10 = 8
So 624-40-8 is a valid CAS Registry Number.

624-40-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,4,5-tetrazinane-3,6-dione

1.2 Other means of identification

Product number -
Other names Tetrahydro-1,2,4,5-tetrazine-3,6-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:624-40-8 SDS

624-40-8Downstream Products

624-40-8Relevant academic research and scientific papers

Reaction of anhydrous zinc chloride with 2,3-thiophenedicarbaldehyde bis(semicarbazone) (2,3BSTCH2) and bis(thiosemicarbazone) (2,3BTSTCH2): Crystal structure of {[C6H5N2S]+[ZnCl3(C6H4N2S)]-} complex

Alomar, Kusa?,Allain, Magali,Richomme, Pascal,Bouet, Gilles

, p. 1591 - 1597 (2015/10/20)

The reaction of anhydrous zinc chloride with 2,3-thiophenedicarbaldehyde bis(semicarbazone) or 2,3-bis(thiosemicarbazone) leads to the formation of compound {[C6H5N2S]+[ZnCl3(C6H4N2S)]-}, where C6H4N2S is thieno[2,3-d]pyridazine, via an elimination-cyclisation reaction of the semicarbazone or the thiosemicarbazone moiety. Crystal structures of thieno[2,3-d]pyridazine and {[C6H5N2S]+[ZnCl3(C6H4N2S)]-} are described. 2015 Institute of Chemistry, Slovak Academy of Sciences

PROCESS FOR STRAIGHTENING KERATIN FIBRES WITH A HEATING MEANS AND DENATURING AGENTS

-

, (2010/03/02)

The invention relates to a process for straightening keratin fibres, comprising: (i) a step in which a straightening composition containing at least two denaturing agents is applied to the keratin fibres, (ii) a step in which the temperature of the keratin fibres is raised, using a heating means, to a temperature of between 110 and 250° C.

1,2,4,5-Tetrahydro-1,2,4,5-tetrazin-2,6-dione (p-Urazine) and Its Conversion into 1,2,4,5-Tetrazine Derivatives

Neugebauer, Franz Alfred,Fischer, Hans

, p. 387 - 395 (2007/10/02)

Cyclization of 4 with phosgene and subsequent hydrogenolysis of the protecting benzyl groups yielded the yet unknown p-urazine (1) which rearranges thermally to the tetrazolidine 2.Compound 1 was dehydrogenated to give 14 which exists in solution in the t

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