1H-Indazole-6-carbaldehyde

1H-Indazole-6-carbaldehyde Suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
Tel: 4006356688 18621169109
Email: market03@meryer.com
Company Name: Energy Chemical  
Tel: 400-0056266
Email: sales8178@energy-chemical.com
Company Name: ZEROSCHEM.CO.,LTD.  
Tel: 10-61256048 13810278579;
Email: sales@zeroschem.com
Company Name: Chemsky(shanghai)International Co.,Ltd.  
Tel: 021-50135380
Email: shchemsky@sina.com

1H-Indazole-6-carbaldehyde manufacturers

1H-Indazole-6-carbaldehyde Basic information
Uses
Product Name:1H-Indazole-6-carbaldehyde
Synonyms:1-H-Indazole-6-carboxaldehyde;6-Formyl-1H-indazole;6-Formylindazole;1H-Indazole-6-carboxaldehyde (9CI);6-indazole carbaldehyde;1H-indazole-6-cabaldehyde;Indazole-6-carboxaldehyde;1H-Indazole-6-carboxaldehyde 95%
CAS:669050-69-5
MF:C8H6N2O
MW:146.15
EINECS:
Product Categories:ALDEHYDE;Building Blocks;Indazole
Mol File:669050-69-5.mol
1H-Indazole-6-carbaldehyde Structure
1H-Indazole-6-carbaldehyde Chemical Properties
Melting point 181-185 °C
Boiling point 358.3±15.0 °C(Predicted)
density 1.368±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka12.49±0.40(Predicted)
form Powder
color White to yellow to brown
InChI1S/C8H6N2O/c11-5-6-1-2-7-4-9-10-8(7)3-6/h1-5H,(H,9,10)
InChIKeyJTWYTTXTJFDYAG-UHFFFAOYSA-N
SMILESO=Cc1ccc2cn[nH]c2c1
CAS DataBase Reference669050-69-5
Safety Information
Risk Statements 36/37/38
Safety Statements 26-36/37/39
WGK Germany 3
HS Code 2933998090
Storage Class11 - Combustible Solids
MSDS Information
1H-Indazole-6-carbaldehyde Usage And Synthesis
Uses1H-indazole-6-carbaldehyde is a useful research chemical.
Synthesis
6-Hydroxymethyl-1H-indazole

916902-55-1

1H-INDAZOLE-6-CARBALDEHYDE

669050-69-5

The general procedure for the synthesis of 1H-indazole-6-carbaldehyde from 1H-indazole-6-methanol was as follows: 1H-indazole-6-methanol (278.0 mg, 1.876 mmol) was dissolved in 10.0 mL of dichloromethane (CH2Cl2) and manganese dioxide (MnO2, 816.0 mg, 9.38 mmol) was added. The reaction mixture was stirred at room temperature overnight. After completion of the reaction, the mixture was filtered and the solids were washed with dichloromethane (2 x 25 mL). The combined filtrates were washed sequentially with water and saturated saline and dried over anhydrous magnesium sulfate (MgSO4). After filtration to remove the desiccant, the solvent was evaporated under reduced pressure to give the crude product 1H-indazole-6-carbaldehyde (270 mg, 98% yield) as a white solid. Mass spectrum (electrospray ionization): m/z 147.1 ([M+H]+).

References[1] Patent: WO2009/54983, 2009, A1. Location in patent: Page/Page column 37-38
[2] Patent: US2008/200535, 2008, A1. Location in patent: Page/Page column 133
[3] Patent: WO2005/44817, 2005, A1. Location in patent: Page/Page column 101-102
[4] Patent: WO2018/177781, 2018, A1. Location in patent: Page/Page column 82; 99-100
1H-Indazole-6-carbaldehyde Preparation Products And Raw materials
Raw materials6-Hydroxymethyl-1H-indazole-->6-Bromoindazole-->N,N-Dimethylformamide-->Manganese dioxide-->Dichloromethane
Preparation Products1-(1H-indazol-6-yl)ethanol
Tag:1H-Indazole-6-carbaldehyde(669050-69-5) Related Product Information
2-Methyl-2H-indazole-3-carbaldehyde 6-Nitro indazole-3-carboxaldehyde 1-Methyl-1H-indazole-3-carbaldehyde 6-Methoxy-1H-indazole-3-carbaldehyde Methyl 1H-indazole-6-carboxylate 1H-indazole-6-carboxylic acid 1-Methyl-1H-indazole-4-carbaldehyde 5-Methyl-3-(1H)indazole carboxaldehyde Indazole 6-Bromo-1H-indazole-3-carbaldehyde 1H-Indazole-3-carbaldehyde 5-Chloro indazole-3-carboxaldehyde 5-Methoxy-1H-indazole-3-carbaldehyde 5-Bromo-1H-indazole-3-carbaldehyde 1-Methyl-1H-indazole-6-carbaldehyde 4-Amino-6-indazolecarboxylic acid methyl ester 1-Methyl-1H-indazole-5-carbaldehyde 7-Methyl-1H-indazole-5-carbaldehyde