N-[2-[[[[1-Methyl-5-[(triphenylmethyl)amino]-1H-pyrazol-4-yl]amino]carbonyl]amino]ethyl]carbamic Acid Tert-butyl Ester CAS NO.:689293-69-4

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N-[2-[[[[1-Methyl-5-[(triphenylmethyl)amino]-1H-pyrazol-4-yl]amino]carbonyl]amino]ethyl]carbamic Acid Tert-butyl Ester CAS NO.:689293-69-4
Details
CAS: 689293-69-4 MF: C31H36N6O3 MW: 540.66 EINECS: 614-818-6
Category
Cephalosporin Intermediates
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Description
Product Name:
N-[2-[[[[1-Methyl-5-[(triphenylmethyl)amino]-1H-pyrazol-4-yl]amino]carbonyl]amino]ethyl]carbamic acid tert-butyl ester
Synonyms:

N-[2-[[[[1-Methyl-5-[(triphenylmethyl)amino]-1H-pyrazol-4-yl]amino]carbonyl]amino]ethyl]carbamicacidtert-butylester;

tert-Butyl[2-({[1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]carbamoyl}amino)ethyl]carbamate;

tert-butyl[2-({[1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]carbamoyl}amino)ethyl]carbamate(RelatedReference);

tert-butyl(2-(3-(1-methyl-5-(tritylamino)-1H-pyrazol-4-yl)ureido)eChemicalbookthyl)carbamate;

Carbamicacid,N-[2-[[[[1-methyl-5-[(triphenylmethyl)amino]-1H-pyrazol-4-yl]amino]carbonyl]amino]ethyl]-,1,1-dimethylethylester;

2-Methyl-3-tritylamino-4-[(2-N-Boc-amino)ethylaminocarbonyl]amino-2H-pyrazole;

2-Methyl-2-propanyl[2-({[1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]carbamoyl}amino)ethyl]carbamate;

tert-butyl[2-({[1-methyl-5-(tritylamino)-1H-pyrazol-4-yl]ca...;

CAS:
689293-69-4
MF:
C31H36N6O3
MW:
540.66
EINECS: 614-818-6
N-[2-[[[[1-Methyl-5-[(triphenylmethyl)amino]-1H-pyrazol-4-yl]amino]carbonyl]amino]ethyl]carbamic acid tert-butyl ester
Boiling Point 680.4±55.0 °C(Predicted)
Density 1.17
Solubility Slightly soluble in chloroform, DMSO, and methanol
Form Solid
Color Grayish white to light brown
Storage temp.
2-8°C(protect from light)

Usage

Uses
1.Field: Medicinal Chemistry / Synthetic Biology​

​​As a synthetic intermediate for bioactive drug molecules (such as antitumor or anti-infective agents), especially as a precursor for drug candidates containing a pyrazole scaffold.​​

​​​2.​​Field: Organic Synthesis / Peptide Chemistry​

​​For amino protection and functionalization in peptide or organic synthesis, serving as a building block with both Boc and Tr protecting groups on the amine.​​

​3.​​Field: New Drug Development / Structure Optimization​

​​As a developmental precursor for pyrazole-based bioactive molecules, from which various potential new drug compounds can be derived through deprotection and derivatization.​​

 

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