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2-Pyrimidinecarboximidic acid, hydrazide (7CI,8CI,9CI) is a chemical compound with the molecular formula C5H6N4O. It is a derivative of pyrimidine, a heterocyclic aromatic organic compound consisting of a six-membered ring with four carbon atoms and two nitrogen atoms. The compound is characterized by the presence of a carboximidic acid group at the 2-position and a hydrazide group attached to it. This specific arrangement of functional groups gives the compound unique chemical properties and potential applications in various fields, such as pharmaceuticals and agrochemicals. The compound's structure and reactivity make it a valuable intermediate in the synthesis of more complex molecules, particularly those with potential biological activity.

1005-03-4

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1005-03-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1005-03-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1005-03:
(6*1)+(5*0)+(4*0)+(3*5)+(2*0)+(1*3)=24
24 % 10 = 4
So 1005-03-4 is a valid CAS Registry Number.

1005-03-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name pyrimidine-2-carbamidrazone

1.2 Other means of identification

Product number -
Other names pyrimidine-2-carboxyamidorazone

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:1005-03-4 SDS

1005-03-4Upstream product

1005-03-4Relevant articles and documents

A one-pot approach to 10-(1H-1,2,3-triazol-1-yl)pyrimido[1,2-a]indoles via aryne-mediated transformations of 3-(pyrimidin-2-yl)-1,2,4-triazines

Kopchuk, Dmitry S.,Chepchugov, Nikolay V.,Khasanov, Albert F.,Kovalev, Igor S.,Santra, Sougata,Nosova, Emiliya V.,Zyryanov, Grigory V.,Majee, Adinath,Rusinov, Vladimir L.,Chupakhin, Oleg N.

, p. 3862 - 3865 (2016)

An efficient synthetic approach toward 10-(1H-1,2,3-triazol-1-yl)pyrimido[1,2-a]indoles, including fluorinated derivatives, has been developed. The transformation of the 1,2,4-triazine ring of readily available 3-(pyrimidin-2-yl)-1,2,4-triazines proceeds

Synthesis of symmetrical di(pyrimidin-2-yl)-1,2,4-triazoles and di(pyrimidin-2-yl)-1,2,4,5-tetrazines

Krivopalov,Bushuev,Gatilov,Shkurko

, p. 1808 - 1816 (2010)

The reactions of pyrimidine-2-carbonitrile and 4,6-dimethylpyrimidine-2- carbonitrile with hydrazine hydrate were investigated. Intermediates in the route of successive transformations of pyrimidine-2-carbonitrile (pyrimidine-2-carbamidrazone and 1,2-bis[amino(pyrimidin-2-yl)methylidene] hydrazine) into trinuclear heterocyclic compounds, viz., symmetrical di(pyrimidin-2-yl)-1,4-dihydro-1,2,4,5-tetrazines and di(pyrimidin-2-yl)-4H-1,2, 4-triazol-4-amines (potential polydentate ligands), were isolated. The oxidative dehydrogenation of di(pyrimidin-2-yl)-1,4-dihydro-1,2,4,5-tetrazines afforded the corresponding 3,6-di(pyrimidin-2-yl)-1,2,4,5-tetrazines.

Organic Compound, Benzoxazole Derivative, and Light-Emitting Element, Light-Emitting Device, and Electronic Device Using Benzoxazole Derivative

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Page/Page column 68, (2012/07/27)

Novel benzoxazole derivatives are provided to reduce driving voltage of light-emitting elements, and to reduce power consumption of light-emitting elements, light-emitting devices, and electronic devices. A benzoxazole derivative represented by the general formula (G1) is provided. Since the benzoxazole derivative represented by the general formula (G1) has an electron-injecting property, the benzoxazole derivative can be suitably used for light-emitting elements, light-emitting devices, and electronic devices.

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