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1H-Pyrazole-3-carboxaldehyde,oxime(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30192-58-6

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30192-58-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30192-58-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,1,9 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 30192-58:
(7*3)+(6*0)+(5*1)+(4*9)+(3*2)+(2*5)+(1*8)=86
86 % 10 = 6
So 30192-58-6 is a valid CAS Registry Number.

30192-58-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1(2)H-pyrazole-3-carbaldehyde oxime

1.2 Other means of identification

Product number -
Other names 1H-PYRAZOLE-3-CARBOXALDEHYDE OXIME

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:30192-58-6 SDS

30192-58-6Downstream Products

30192-58-6Relevant academic research and scientific papers

Energetic C-trinitromethyl-substituted pyrazoles: Synthesis and characterization

Zhang, Yiying,Li, Yanan,Hu, Jianjian,Ge, Zhongxue,Sun, Chenghui,Pang, Siping

, p. 1524 - 1529 (2019)

A new family of C-trinitromethyl-substituted pyrazoles was designed and obtained in good yields by the reaction of N2O4 with the pyrazolecarbaldehyde oxime followed by further N-nitration and C-nitration. All of the new compounds were fully characterized by IR and NMR spectroscopy, elemental analysis and differential scanning calorimetry (DSC). Compounds 2 and 3 were further confirmed by X-ray crystallography. These pyrazole derivatives have good densities, positive enthalpies of formation and acceptable sensitivity values. Theoretical calculations carried out using Gaussian 03 and EXPLO5 program demonstrate good to excellent detonation velocities and pressures in the range of ADN and HMX. Compound 3 exhibiting a positive oxygen balance, high specific impulse and moderate thermal stability is a promising high energy density oxidizer.

1-nitro-3-trinitro methyl pyrazol compound

-

Paragraph 0020; 0021; 0022; 0039; 0040; 0041, (2019/02/04)

The invention discloses a 1-nitro-3-trinitro methyl pyrazol compound. A structural formula of the 1-nitro-3-trinitro methyl pyrazol compound is as shown in a formula (I): (shown in the specification).The 1-nitro-3-trinitro methyl pyrazol compound is mainly used in the field of energetic materials.

3-trinitromethylpyrazole compound

-

Paragraph 0008; 0020-0024; 0028; 0040-0044; 0048, (2019/02/04)

The invention discloses a 3-trinitromethylpyrazole compound, which is of a structural formula as shown by a formula (I) as shown in the following descriptions. The 3-trinitromethylpyrazole compound ismainly used in the field of energetic materials.

3-heliacal dinomethyl-5-nitropyrazole hydrazine salt compound

-

Paragraph 0022-0030; 0050-0058, (2019/04/02)

The invention discloses a 3-heliacal dinomethyl-5-nitropyrazole hydrazine salt compound. A structural formula of the compound is shown as (I). The compound is mainly used in the field of explosives.

Copper(ii)-promoted direct conversion of methylarenes into aromatic oximes

Yu, Jiatao,Lu, Ming

supporting information, p. 7397 - 7401 (2015/07/15)

A simple and efficient catalytic system for direct conversion of methylarenes into aromatic oximes has been developed, with Cu(OAc)2 as catalyst, NHPI (N-Hydroxyphthalimide) as additive, TBN (tert-butyl nitrite) as both the nitrogen source and the oxidant. This process proceeds under mild conditions, tolerates a wide range of substrates, affording the targeted aromatic oximes in 63-86% yields.

Copper(II)-promoted direct conversion of methylarenes into aromatic oximes

Yu, Jiatao,Lu, Ming

supporting information, p. 7397 - 7401 (2015/11/27)

A simple and efficient catalytic system for direct conversion of methylarenes into aromatic oximes has been developed, with Cu(OAc)2 as catalyst, NHPI (N-Hydroxyphthalimide) as additive, TBN (tert-butyl nitrite) as both the nitrogen source and the oxidant. This process proceeds under mild conditions, tolerates a wide range of substrates, affording the targeted aromatic oximes in 63-86% yields.

MALONONITRILE COMPOUND AND USE THEREOF

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Page/Page column 46, (2008/06/13)

A nitrile compound shown by the formula (1) has an excel lent pesticidal activity and it is useful as an active ingredient of pesticide.

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