784142-98-9 Usage
Ethyl ester derivative
1H-Pyrazole-5-carboxylic acid This indicates that the compound is derived from 1H-pyrazole-5-carboxylic acid and has an ethyl ester group attached.
Contains a 3-bromophenyl group
The presence of a bromine atom on the phenyl ring This indicates that the compound has a bromine atom attached to the phenyl ring, which can affect its chemical properties and reactivity.
Contains a methyl group
A carbon atom bonded to three hydrogen atoms This indicates that the compound has a methyl group (a carbon atom bonded to three hydrogen atoms) attached, which can affect its chemical properties and reactivity.
Used in organic synthesis and pharmaceutical research
Potential applications in drug or material development This indicates that the compound is used in the synthesis of other compounds and has potential applications in the development of new drugs or materials.
Handle with care and follow safety protocols in the laboratory
Safety considerations This is a reminder to handle the chemical with care and follow proper safety protocols when working with it in a laboratory setting.
Check Digit Verification of cas no
The CAS Registry Mumber 784142-98-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,4,1,4 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 784142-98:
(8*7)+(7*8)+(6*4)+(5*1)+(4*4)+(3*2)+(2*9)+(1*8)=189
189 % 10 = 9
So 784142-98-9 is a valid CAS Registry Number.
784142-98-9Relevant academic research and scientific papers
PYRAZOL DERIVATIVES
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Page/Page column 20, (2009/02/11)
The invention is concerned with novel pyrazol derivatives of formula (I), wherein R1, R2, R3, R4, X and Y are as defined herein, as well as physiologically acceptable salts thereof. These compounds are antagonists of CCR-2 receptor and/or CCR-5 receptor and can be used as medicaments.
SUBSTITUTED PYRAZOLES AS PPAR AGONISTS
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Page/Page column 72, (2010/02/12)
A compound of formula (I) and pharmaceutically acceptable salts, solvates and hydrolysable esters thereof (I) wherein: p is O or 1; q is O or 1; R1 and R2 are independently H or C1-3 alkyl; R3 and R4 are independently H, C1-6 alkyl, -OC1-6 alkyl, halogen, OH, C2-6 alkenyl or CF3; R5 is H, C1-6 alkyl (optionally substituted by one or more halogens, -COphenyl, OC1-6 alkyl, phenyl morpholino or C2-6 alkenyl. R6 is C1-6 alkyl, halogen, -OCH2 phenyl, phenyl (optionally substituted by C1-3 alkiyl), morpholino, pyrrolidino, piperidino, thiophenyl, furanyl pyridinyl or -OC2-6 alkenyl. These compounds activate the alpha and gamma subtypes fo the hppar receptor and are useful e.g. in the treatment of diabetes, dyslipidemia or syndrome X.
BIARYL SUBSTITUTED PYRAZOLES AS SODIUM CHANNEL BLOCKERS
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Page 57, (2008/06/13)
Biaryl substituted pyrazole compounds are sodium channel blockers useful for the treatment of pain and other conditions. Pharmaceutical compositions comprise an effective amount of the instant compounds, either alone, or in combination with one or more th
