methyl 1H-indazole-3-carboxylate CAS 43120-28-1

Molecular Formula: C9H8N2O2
Molecular Weight: 176.17
Purity: ≥95%
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methyl 1H-indazole-3-carboxylate CAS 43120-28-1

methyl 1H-indazole-3-carboxylate CAS 43120-28-1 C9H8N2O2 in stock, hot selling to Europe and Canada

CAS 43120-28-1 Basic Parameter

Synonyms 1H-INDAZOLE-3-CARBOXYLICACIDMETHYLESTER;3-Indazolecarboxylicacidmethylester;methyl1H-indazole-3-carboxylate(SALTDATA:FREE);1H-Indazole-3-CarboxylicAcidMethylEster(WX6;Indazole-3-carboxylicAcidMethylEster;METHYLINDAZOLYL-3-CARBOXYLATE
CAS NO 43120-28-1
Molecular Formula C9H8N2O2
Molecular Weight 176.17
EINECS 251-228-4
Melting Point 162-163℃
Boiling Point 345.2±15.0 °C(Predicted)
Density 1.324
Storage Sealed in dry, room temperature
Solubility Soluble in chloroform (a little), methanol (a little)
Form Solid
Color White to off-white

CAS 43120-28-1 Picture

cas 43120-28-1, C9H8N2O2

What is methyl 1H indazole 3 carboxylate?

Methyl 1H-indazole-3-carboxylate is a synthetic cannabinoid that is structurally related to the natural cannabinoid, anandamide. It has been shown to be a potent activator of the CB2 receptor and to inhibit spontaneous activity in mice.

What is methyl ester of isonicotinic acid?

Methyl isonicotinate is a toxic compound, which is used as a semiochemical. Other names for this compound are 4-pyridine carboxylic acid, and isonicotinic acid methyl ester. This compound is slightly toxic to the human body. It has an irritating effect on the eyes, skin, and respiratory tract.

What is 1H indole 3 amine?

1H-Indole-3-amine is a fluorescent compound that can be detected using a fluorescence detector. The locomotor activity of mice and the hippocampal formation in rats have been shown to be decreased by 1H-indole-3-amine.

What is 1H indole 1 acetic acid?

Indole-1-acetic acid is an indolyl carboxylic acid that is acetic acid in which one of the methyl hydrogens is substituted by an indol-1-yl group. It is a monocarboxylic acid and an indolyl carboxylic acid. It is functionally related to an acetic acid.


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