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15967-75-6

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15967-75-6 Usage

Structure

Five-membered ring with two nitrogen atoms and an ethenyl group attached to the first position, and two methyl groups attached to the third and fifth positions This describes the arrangement of atoms in the compound and the specific groups that are present.

Derivative of pyrazole

The compound is a derivative of pyrazole, which is a five-membered ring containing two nitrogen atoms This indicates that the compound is derived from pyrazole and has similar properties.

Building block in organic synthesis and pharmaceutical research

The compound is commonly used as a building block in organic synthesis and pharmaceutical research This indicates that the compound is useful for creating more complex molecules and has applications in the field of chemistry and medicine.

Ligand in coordination chemistry

The compound can be used as a ligand in coordination chemistry This indicates that the compound can bind to metal ions and form coordination complexes, which have applications in various fields such as catalysis and materials science.

Wide range of applications

The compound's structure and properties make it useful for a wide range of applications in chemical and biological research This indicates that the compound has potential uses in various areas of research and can contribute to the advancement of knowledge in these fields.

Check Digit Verification of cas no

The CAS Registry Mumber 15967-75-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,6 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15967-75:
(7*1)+(6*5)+(5*9)+(4*6)+(3*7)+(2*7)+(1*5)=146
146 % 10 = 6
So 15967-75-6 is a valid CAS Registry Number.

15967-75-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethenyl-3,5-dimethylpyrazole

1.2 Other means of identification

Product number -
Other names Pyrazole,1-vinyl-3,5-dimethyl

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:15967-75-6 SDS

15967-75-6Relevant articles and documents

N-2-(Azol-1(2)-yl)ethyliminodiacetic acids: A novel series of Gd(III) chelators as T2 relaxation agents for magnetic resonance imaging

Lopez, Pilar,Seipelt, Christa G.,Merkling, Patrick,Sturz, Laszlo,Alvarez, Jose,Doelle, Andreas,Zeidler, Manfred D.,Cerdan, Sebastian,Ballesteros, Paloma

, p. 517 - 527 (2007/10/03)

The synthesis, physicochemical properties, and toxicological implications of a novel series of N-2-(azol-1(2)-yl)ethyliminodiacetic acids, useful as contrast agents for magnetic resonance imaging are reported. Compounds were prepared by alkylation of methyl iminodiacetate with N-2-bromoethylazoles and subsequent hydrolysis. Stability constants of the corresponding Gd(III) complexes and T1 and T2 relaxivities were determined and interpreted in terms of optimized geometries obtained by semiempirical PM3 calculations. Compounds show increased T2 relaxivity and decreased toxicity in vitro as compared to EDTA-Gd(III) complexes. Copyright (C) 1999 Elsevier Science Ltd.

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