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3112-31-0

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3112-31-0 Usage

Chemical Properties

white crystalline powder

Purification Methods

It crystallises from water as a monohydrate, or EtOH. Dry it in a vacuum at 100o. The dimethyl ester crystallises from *C6H6 with m 155o. [Beilstein 25 III/IV 1047.]

Check Digit Verification of cas no

The CAS Registry Mumber 3112-31-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,1 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3112-31:
(6*3)+(5*1)+(4*1)+(3*2)+(2*3)+(1*1)=40
40 % 10 = 0
So 3112-31-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H4N2O4/c8-4(9)2-1-3(5(10)11)7-6-2/h1H,(H,6,7)(H,8,9)(H,10,11)/p-2

3112-31-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-pyrazole-3,5-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names 1H-Pyrazole-3,5-dicarboxylic acid

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:3112-31-0 SDS

3112-31-0Relevant articles and documents

SYNTHESIS OF NEW MACROCYCLIC POLYETHER DI- OR TETRAESTER LIGANDS CONTAINING PYRAZOLE UNITS

Elguero, J.,Navarro, P.,Franco, M. I. Rodriguez

, p. 425 - 428 (1984)

A new series of macrocyclic polyether - diester compounds containing one or two pyrazole rings (NH or N-methyl substituted) have been prepared by treating 3,5-pyrazolyldicarbonyl chlorides with tetraethylene glycol in the presence of triethylamine.Their complexation abilities towards the shift reagent Eu(Fod)3 have been studied by 1H NMR in CDCl3 solution.

Combining 1,2,4-triazole and pyrazole frameworks for new insensitive energetic materials

Chen, Jieyi,Cheng, Guangbin,Dai, Changhao,Tang, Jie,Yang, Hongwei

, p. 17960 - 17965 (2021/10/12)

A new symmetric compound 3,5-bis(3-amine-4H-1,2,4-triazole)-1H-pyrazole and a series of corresponding energetic salts5-9were synthesized. All the new compounds were fully characterized by spectroscopy (IR, NMR, and elemental) analyses and differential scanning calorimetry (DSC). Compound6was further investigated by X-ray crystal-structure analysis. Various performance tests of all the compounds, such as density, thermal behavior, mechanical sensitivity and detonation property, were tested. All the target compounds showed relatively positive calculated heat of formation (24.9 to 2396.4 kJ mol?1), good mechanical sensitivity (IS > 24 J, FS > 280 N) and acceptable detonation property (D> 7400 m s?1,P> 19.5 GPa). In particular, energetic salt9exhibits prominent detonation property (D> 8964 m s?1,P> 37.1 GPa) and excellent sensitivity (IS > 40 J, FS > 360 N), which show its potential application prospects as a new high energy insensitive material.

Strategy for the Synthesis of pyrazolo[5,1-d][1,2,5]triazepinones, a new heterocyclic system

Kharaneko

, p. 1322 - 1325 (2016/10/26)

A preparative procedure has been developed for the synthesis of 4-oxo-7-phenyl-5,8-dihydro-4H-pyrazolo[ 5,1-d][1,2,5]triazepine-2-carbohydrazide, the first representative of a new heterocyclic system, by recyclization of methyl 4-oxo-6-phenyl-4H-pyrazolo[5,1-c][1,4]oxazine-2-carboxylate with hydrazine hydrate.

Efficient photochemical water oxidation by a dinuclear molecular ruthenium complex

Laine, Tanja M.,K?rk?s, Markus D.,Liao, Rong-Zhen,A?kermark, Torbj?rn,Lee, Bao-Lin,Karlsson, Erik A.,Siegbahn, Per E. M.,A?kermark, Bj?rn

supporting information, p. 1862 - 1865 (2015/01/30)

Herein is described the preparation of a dinuclear molecular Ru catalyst for H2O oxidation. The prepared catalyst mediates the photochemical oxidation of H2O with an efficiency comparable to state-of-the-art catalysts.

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