Przejdź do
300780
Ethyl 4-pyrazolecarboxylate
99%
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Informacje o tej pozycji
Wzór empiryczny (zapis Hilla):
C6H8N2O2
Numer CAS:
Masa cząsteczkowa:
140.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
99%
Form:
powder
assay
99%
form
powder
bp
138-140 °C/3 mmHg (lit.)
mp
78-80 °C (lit.)
functional group
ester
SMILES string
CCOC(=O)c1cn[nH]c1
InChI
1S/C6H8N2O2/c1-2-10-6(9)5-3-7-8-4-5/h3-4H,2H2,1H3,(H,7,8)
InChI key
KACZQOKEFKFNDB-UHFFFAOYSA-N
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Klasa składowania
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
Jon C Antilla et al.
The Journal of organic chemistry, 69(17), 5578-5587 (2004-08-17)
This paper details the copper-catalyzed N-arylation of pi-excessive nitrogen heterocycles. The coupling of either aryl iodides or aryl bromides with common nitrogen heterocycles (pyrroles, pyrazoles, indazoles, imidazoles, and triazoles) was successfully performed in good yield with catalysts derived from diamine
J F Schindler et al.
Journal of protein chemistry, 15(8), 737-742 (1996-11-01)
Improved and efficient techniques have led to an explosive growth in the application of site-directed mutagenesis to the study of enzymes. However, the limited availability of only those 20 amino acids that are translated by the genetic code has prevented
Numer pozycji handlu globalnego
| SKU | NUMER GTIN |
|---|---|
| 300780-500MG | 04061832993430 |