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1,3-Benzenedicarbonitrile, 5-[(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)methyl]- is a complex organic compound with the chemical formula C12H8N6O4. It is characterized by a benzene ring with two carbonitrile groups at the 1 and 3 positions, and a 1,2,4-triazin-3(2H)-one moiety attached to the 5 position of the benzene ring. 1,3-Benzenedicarbonitrile, 5-[(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)methyl]- is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is a white crystalline solid that is insoluble in water but soluble in organic solvents. The compound is synthesized through a series of chemical reactions involving the formation of the triazine ring and subsequent attachment to the benzene dicarbonitrile structure. It is important to handle 1,3-Benzenedicarbonitrile, 5-[(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)methyl]- with care due to its potential toxicity and reactivity.

61958-95-0

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61958-95-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61958-95-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,5 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 61958-95:
(7*6)+(6*1)+(5*9)+(4*5)+(3*8)+(2*9)+(1*5)=160
160 % 10 = 0
So 61958-95-0 is a valid CAS Registry Number.

61958-95-0SDS

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 5-(3,5-dioxo-4,5-dihydro-3H-[1,2,4]triazin-2-ylmethyl)-isophthalonitrile

1.2 Other means of identification

Product number -
Other names 5-(3,5-Dioxo-4,5-dihydro-3H-[1,2,4]triazin-2-ylmethyl)-isophthalonitrile

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:61958-95-0 SDS

61958-95-0Upstream product

61958-95-0Downstream Products

61958-95-0Relevant academic research and scientific papers

Anticoccidial derivatives of 6 azauracil. I. Enhancement of activity by benzylation of nitrogen 1. Observations on the design of nucleotide analogues in chemotherapy

Mylari,Miller,Howes Jr.,Figdor,Lynch,Koch

, p. 475 - 483 (2007/10/09)

Benzylation of 6-azauracil at N-1 (which corresponds to the point of attachment of the ribose phosphate unit in pyrimidine nucleotides) has been found to augment its anticoccidial activity fourfold. The high potency of 1-benzyl-6-azauracil is ascribed to a combination of intrinsic activity, efficient oral absorption, and a moderate rate of excretion. Metabolism experiments using 1-benzyl-6-azauracil labeled with 14C in the heterocycle and (separately) in the side chain showed that, in the drug accounted for, no cleavage had occurred. Additional activity increases were achieved by introducing small, electron-withdrawing substituents in the meta and/or para position(s) of the benzyl group. One of the most active derivatives, 1-(3-cyanobenzyl)-6-azauracil, is about 16 times as potent as 6-azauracil.

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