689294-25-5

Basic information

• Product Name: Phenyl (5-aMino-1-Methyl-1H-pyrazol-4-yl)carbaMate, 95%
• Synonyms: Phenyl (5-aMino-1-Methyl-1H-pyrazol-4-yl)carbaMate, 95%
• CAS NO: 689294-25-5
• Molecular Formula: C₁₁H₁₂N₄O₂
• Molecular Weight: 232.23858
• Mol File: 689294-25-5.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Phenyl (5-aMino-1-Methyl-1H-pyrazol-4-yl)carbaMate, 95%(CAS DataBase Reference)
• NIST Chemistry Reference: Phenyl (5-aMino-1-Methyl-1H-pyrazol-4-yl)carbaMate, 95%(689294-25-5)
• EPA Substance Registry System: Phenyl (5-aMino-1-Methyl-1H-pyrazol-4-yl)carbaMate, 95%(689294-25-5)

Safety Data

• Hazardous Substances Data: 689294-25-5(Hazardous Substances Data)

Usage

General Description

Phenyl (5-amino-1-methyl-1H-pyrazol-4-yl) carbamate, which is available in a concentration of 95%, is a chemical compound that belongs to the carbamate class of chemicals. It is commonly used in various industrial applications, including as a pharmaceutical intermediate in the synthesis of certain drugs. Phenyl (5-aMino-1-Methyl-1H-pyrazol-4-yl)carbaMate, 95% is characterized by its phenyl group, amino group, and pyrazole ring structure, which make it useful in the modification of other molecules for specific functions. The high purity level of 95% ensures that it is suitable for use in research and manufacturing processes where precise control over composition is essential.

Upstream product

• 20055-01-0 4,5-diamino-1-methylpyrazole sulfate 
• 1885-14-9 phenyl chloroformate 
• 45514-38-3 1-methyl-1H-pyrazole-4,5-diamine 

Downstream Products

• 689294-26-6 1-methyl-4-phenoxycarbonylamino-5-triphenylmethylaminopyrazole 
• 689293-69-4 4-(3-{2-[(tert-butoxycarbonyl)amino]ethyl}ureido)-1-methyl-5-triphenylmethylaminopyrazole 

Relevant articles and documents

SOLID FORMS OF CEFTOLOZANE AND PROCESSES FOR PREPARING

The instant invention is related to a novel solid form of ceftolozane sulfate (the DMAc solvate of ceftolozane sulfate (Form 3)), compositions comprising ceftolozane sulfate DMAc solvate (Form 3), synthesis of Form 3 and an improved crystallization proces

Synthesis and SAR of novel parenteral anti-pseudomonal cephalosporins: Discovery of FR264205

We describe herein the synthesis and biological evaluation of a series of novel cephalosporins with potent activity against Pseudomonas aeruginosa. Introduction of various amino groups to the 4-position of a 3-amino-2-methylpyrazole cephalosporin 3-side c

CEPHEM COMPOUNDS

The present invention relates to a compound of the formula [I]: wherein R1 is lower alkyl, hydroxy(lower)alkyl or halo(lower)alkyl, and R2 is hydrogen or amino protecting group, or R1 and R2 are bonded together and form lower alkylene or lower alkenylene; R3 is hydrogen or lower alkyl; R4 is ; R5 is carboxy or protected carboxy; and R6 is amino or protected amino, or a pharmaceutically acceptable salt thereof, a process for preparing a compound of the formula [I], and a pharmaceutical composition comprising a compound of the formula [I] in admixture with a pharmaceutically acceptable carrier.