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2,3-dihydro-4H-pyrazolo[3,4-d][1,2,3]triazin-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19818-50-9

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19818-50-9 Usage

Structure

Heterocyclic ring compound

Derivative

Member of the pyrazolotriazine family

Common Use

Pharmaceutical research as a potential drug candidate

Pharmacological Activities

Anti-inflammatory
Antitumor
Antiviral

Versatility

Molecular structure and functional groups make it a versatile scaffold for synthesis

Potential Therapeutic Applications

Synthesis of novel compounds

Bioactive Applications

Investigated for agricultural and veterinary use

Check Digit Verification of cas no

The CAS Registry Mumber 19818-50-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,1 and 8 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 19818-50:
(7*1)+(6*9)+(5*8)+(4*1)+(3*8)+(2*5)+(1*0)=139
139 % 10 = 9
So 19818-50-9 is a valid CAS Registry Number.

19818-50-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dihydropyrazolo[3,4-d]triazin-4-one

1.2 Other means of identification

Product number -
Other names 4-Hydroxy-pyrazolo<3,4-d>-s-triazin

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:19818-50-9 SDS

19818-50-9Downstream Products

19818-50-9Relevant academic research and scientific papers

Pyrazole Derivatives. 5. Synthesis and Antineoplastic Activity of 3-(2-Chloroethyl)-3,4-dihydro-4-oxopyrazolo-1,2,3,5-tetrazine-8-carboxamide and Related Compounds

Cheng, C.C.,Elslager, Edward F.,Werbel, Leslie M.,Priebe, S.R.,Leopold, Wilbur R.

, p. 1544 - 1547 (2007/10/02)

Two pyrazolotetrazine derivatives were synthesized as the analogous prodrugs of the light-sensitive antineoplastic agents dacarbazine and BIC.Both the pyrazole derivatives are stable under ordinary light illumination.Biological evaluation of these pyrazoles revealed that compound containing a 2-chloroethyl function (6a) demonstrated good antineoplastic activity in experimental animals, but the one containing a methyl function (6b) was inactive.The inactivity of compound 6b may suggest that compound 6a and related imidazotetrazines may simply act as biological alkylati ng agents per se rather than as prodrugs.The information could also imply that the postulated dealkylation mechanism for the triazene derivatives should be reexamined.

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