1H-indazole-6-carboxylic acid

1H-indazole-6-carboxylic acid Structure
CAS No.
704-91-6
Chemical Name:
1H-indazole-6-carboxylic acid
Synonyms
6-Carboxy-1H-indazole;INDAZOLE-6-CARBOXYLIC ACID;1H-Indazole-6-carboylic acid;1H-Indazol-6-carboxylic acid;1-H-indazole-6-carboxyle acid;1H-INDAZOLE-6-CARBOXYLIC ACID;6-(1H)INDAZOLE CARBOXYLIC ACID;1H-Indazole-6-carboxylic acid 97%;1H-Indazole-6-carboxylic acid, 97%+;1H-Indazole-6-carboxylic acid (7CI, 8CI, 9CI, ACI)
CBNumber:
CB3113514
Molecular Formula:
C8H6N2O2
Molecular Weight:
162.15
MOL File:
704-91-6.mol
MSDS File:
SDS
Modify Date:
2023/4/23 13:52:06

1H-indazole-6-carboxylic acid Properties

Melting point 302-307 °C
Boiling point 443.7±18.0 °C(Predicted)
Density 1.506±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka 4.01±0.30(Predicted)
form Crystalline Powder
color White to light brown
InChIKey DNCVTVVLMRHJCJ-UHFFFAOYSA-N

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338
WGK Germany  3
HazardClass  IRRITANT
HS Code  29339980

1H-indazole-6-carboxylic acid price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 702420 1H-Indazole-6-carboxylic acid 97% 704-91-6 1G ₹7772.35 2022-06-14 Buy
Product number Packaging Price Buy
702420 1G ₹7772.35 Buy

1H-indazole-6-carboxylic acid Chemical Properties,Uses,Production

Uses

1H-Indazole-6-carboxylic Acid is used as a reagent to synthesize azabicyclic aryl amides, which act as α7 nicotinic acetylcholine receptor agonists.

Preparation

Synthesis of 1H-indazole-6-carboxylic acid, H2L3: MeL3Ac (1.0 g; 4.6 mmol) was dissolved in 40 mL THF, and this solution was added to a 40 mL aqueous solution of lithium hydroxide (5.0 g; 210 mmol). The resulting suspension was heated at reflux with vigorous stirring overnight, after which time the solution was concentrated under vacuum to remove the organic phase. The resulting solution was filtered, adjusted to pH 3 with conc. HCl, to precipitate the product as a pale brown solid, which was filtered, washed with water and dried under vacuum. Yield 315 mg, 43%. mp 292–296 °C (decomp);
δH (500 MHz, d6-DMSO): 7.67 (dd, 1H, J = 8.3, 1.0 Hz, H4 ), 7.85 (dd, 1H, J = 8.3, 0.8 Hz, H3 ), 8.15 (s, 1H, H6 ), 8.18 (d, 1H, J = 0.8 Hz, H2 ), 13.24 (br s, 2H, H1 & H5 ); δC (125 MHz, CD3OD): 114.1, 122.0, 122.6, 127.1, 130.6, 135.2, 141.4, 170.4; HRMS-ESI m/z: found: 163.0503; C8H7N2O2 requires: 163.0502 [M + H+ ]; ˉνmax/cm?1 (KBr): 3258 br, 2864 br, 2582 br, 1679 s, 1579 m, 1518 m, 1425 m, 1230 s, 1087 m, 954 s, 857 m, 762 m, 693 m.

1H-indazole-6-carboxylic acid Preparation Products And Raw materials

Raw materials

Preparation Products

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1H-indazole-6-carboxylic acid Spectrum

INDAZOLE-6-CARBOXYLIC ACID 1H-INDAZOLE-6-CARBOXYLIC ACID 6-(1H)INDAZOLE CARBOXYLIC ACID 1H-Indazole-6-carboxylic acid 97% 1H-Indazole-6-carboxylic acid, 97%+ 6-Carboxy-1H-indazole 1-H-indazole-6-carboxyle acid 1H-Indazol-6-carboxylic acid 1H-Indazole-6-carboylic acid 1H-Indazole-6-carboxylic acid (7CI, 8CI, 9CI, ACI) 704-91-6 Indazoles Building Blocks Indazole pharmacetical