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15870-75-4

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15870-75-4 Usage

General Description

6-bromo-4-methyl-1,2,4-triazine-3,5(2H,4H)-dione is a chemical compound with the molecular formula C4H3BrN3O2. It is a heterocyclic compound containing a triazine ring with a bromine atom and a methyl group attached. 6-bromo-4-methyl-1,2,4-triazine-3,5(2H,4H)-dione is commonly used in the pharmaceutical industry as a building block for the synthesis of various biologically active compounds. It is also used in organic synthesis as a reagent for the preparation of a wide range of functionalized triazine derivatives. Additionally, it has potential applications in agrochemicals, colorants, and materials science due to its unique chemical and physical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 15870-75-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,7 and 0 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15870-75:
(7*1)+(6*5)+(5*8)+(4*7)+(3*0)+(2*7)+(1*5)=124
124 % 10 = 4
So 15870-75-4 is a valid CAS Registry Number.

15870-75-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromo-4-methyl-2H-1,2,4-triazine-3,5-dione

1.2 Other means of identification

Product number -
Other names 6-Brom-4-methyl-3,5-dioxo-2,3,4,5-tetrahydro-as-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:15870-75-4 SDS

15870-75-4Relevant articles and documents

DERIVATIVES OF TRIAZINES AND URACILS, THEIR PREPARATION AND THEIR APPLICATION IN HUMAN THERAPEUTICS

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Page/Page column 18-19, (2010/04/03)

The present invention relates to derivatives of general formula I wherein : - W represents nitrogen, - R1 represents: ? a hydrogen or a linear or branched C1-C5 alkyl radical or, ? a C1-C3 alkyl radical substituted with groups such as trifluoromethyl, nitrile, hydroxy, C1-C3 alcoxy, C3-C6 alkoxyalkoxy, indolyl, thiophenyl, oxothiophenyl, C1-C3 N-alkylcarbamoyl groups or, ? a phenyl or pyridyl or naphthyl, or thiophenyl group optionally substituted with one or more groups such as halogen atoms, nitro, nitrile, trifluoromethyl, vinyl, methylsulfanyl, linear branched C1-C4 alkyl, linear or branched C1-C3 alkoxy groups, ? a C6 2-oxocycloalkyl radical - R2 represents a methyl or heptyl, - m, n are equal to 1, - V represents CH2, - X-Y represents -N- (C=O) -, -CH-O-, - Z represents a phenyl group substituted with one or more trifluoromethyl groups, halogen atoms or linear C1-C4 alkyl groups.

1,2,4-TRIAZINES DERIVATIVES, PREPARATION THEREOF AND USE THEREOF IN HUMAN THERAPEUTICS

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Page/Page column 20, (2010/02/13)

The invention relates to 3,5-dioxo-(2H,4H)-1,2,4-triazine derivatives of general formulae (I or II), in which in particular: R1 represents hydrogen, a linear or branched C1-C6 alkyl or alkoxy radical, a C5-C6 cycloalkyl radical, a phenyl (C1-C2) alkyl radical or a phenyl radical;-R2 represents hydrogen, a linear or branched Cl-C7alkyl radical, or a C1-C6 alkyl radical substituted with groups such as trifluoromethyl or phenyl;- linker represents a C2-C6 alkyl chain or -(CH2)n-O- (n = 2 to 5), - R3 represents a group of general formula below for which X = O, linker can be connected to the ortho-, meta- or para-positions of the aromatic of the group R3, R4, R5, R6, R7 and R8 represent hydrogen or fluorine, R9, Rio and R11 represent hydrogen or a linear or branched Cl-C5 alkyl group, in particular R9 and Rio represent the methyl group and R11 represents hydrogen or the ethyl group.

1,3-dimethyl-5-fluoro-6-azauracil and some 5-bromo-6-azauracil derivatives.

Durr

, p. 288 - 289 (2007/10/09)

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