1H-indazole-7-carboxylic acid

1H-indazole-7-carboxylic acid Structure
CAS No.
677304-69-7
Chemical Name:
1H-indazole-7-carboxylic acid
Synonyms
7-Carboxy-1H-indazole;CgH6N2O2;Niraparib Intermediate4;7-INDAZOLE CARBOXYLIC ACID;7-INDAZOLE CARBOXYLLIC ACID;1H-Indazole-7-carboxylic aid;1H-Indazol-7-carboxylic acid;1H-INDAZOLE-7-CARBOXYLIC ACID;7-(1H)Indazole carboxylic acid;677304-69-7
CBNumber:
CB9197275
Molecular Formula:
C8H6N2O2
Molecular Weight:
162.15
MOL File:
677304-69-7.mol
Modify Date:
2023/12/25 17:47:29

1H-indazole-7-carboxylic acid Properties

Melting point ca 240℃
Boiling point 443.7±18.0 °C(Predicted)
Density 1.506±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly)
form Crystalline Powder
pka 3.71±0.10(Predicted)
color White to yellow

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a
HS Code  29339980
NFPA 704
1
2 0

1H-indazole-7-carboxylic acid price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) ANV00147 1H-Indazole-7-carboxylic acid AldrichCPR 677304-69-7 1G ₹62795.83 2022-06-14 Buy
Product number Packaging Price Buy
ANV00147 1G ₹62795.83 Buy

1H-indazole-7-carboxylic acid Chemical Properties,Uses,Production

Uses

1H-indazole-7-carboxylic Acid is an inhibitor of nitric oxide synthases.

Preparation

Synthesis of 1H-indazole-7-carboxylic acid, H2L4: To 60 mL anhydrous toluene under a nitrogen atmosphere was added methyl-2-amino-3-methylbenzoate (1.8 g, 11 mmol) and KOAc (560 mg, 5.7 mmol), and the mixture heated to reflux, at which time acetic anhydride (3.2 mL, 34 mmol) was added and the mixture stirred at reflux for 10 min. Isoamyl nitrite (2.3 mL, 18 mmol) was added over 30 min and the mixture refluxed overnight. On cooling, the mixture was filtered and evaporated to dryness to give 1.6 g of a pale brown solid, which analysed for methyl 1H-indazole-7-carboxylate. This material was taken up in 40 mL THF, added to a solution of LiOH (5 g, 210 mmol) in 40 mL water, and heated at reflux for 48 h. On cooling, the mixture was concentrated on a rotary evaporator and the resulting aqueous phase filtered and adjusted to pH 4 with dilute HCl, to precipitate the product, which was filtered, washed with water and dried under vacuum. Yield 810 mg, 45%; mp 218–222 °C (decomp);
δH (500 MHz, d6-DMSO): 7.23 (t, 1H, J = 7.5 Hz, H4 ), 7.97 (dd, 1H, J = 7.5, 1.0 Hz, H3 ), 8.06 (dd, 1H, J = 7.8, 0.8 Hz, H5 ), 8.21 (s, 1H, H2 ), 13.1 (br s, 2H, H1 & H6 ); δc (125 MHz, d6-DMSO): 113.7, 120.1, 124.6, 126.5, 129.0, 134.3, 138.0, 167.0; HRMS-ESI m/z: found: 163.0503; C8H7N2O2 requires: 163.0502 [M + H+ ]; ˉνmax/cm?1 (KBr): 3316 s br, 1700 s, 1619 m, 1592 m, 1509 m, 1285 s, 1201 m, 1145 m, 1078 m, 1056 w, 943 m, 858 s, 745 s, 638 m, 601 m.

1H-indazole-7-carboxylic acid Preparation Products And Raw materials

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1H-indazole-7-carboxylic acid Spectrum

7-INDAZOLE CARBOXYLLIC ACID 1H-INDAZOLE-7-CARBOXYLIC ACID 7-INDAZOLE CARBOXYLIC ACID 7-(1H)Indazole carboxylic acid 1H-Indazol-7-carboxylic acid 7-Carboxy-1H-indazole Niraparib Intermediate4 677304-69-7 CgH6N2O2 1H-Indazole-7-carboxylic aid 677304-69-7 Amines C8 Chemical Synthesis New Products for Chemical Synthesis Nitrogen Compounds Organic Building Blocks Indazoles Building Blocks Indazole