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3-(HYDROXYMETHYL)INDAZOLE

Product Name
3-(HYDROXYMETHYL)INDAZOLE
CAS No.
64132-13-4
Chemical Name
3-(HYDROXYMETHYL)INDAZOLE
Synonyms
1H-Indazol-3-Methanol;1H-Indazole-3-methanol;2H-indazol-3-ylmethanol;3-(HYDROXYMETHYL)INDAZOLE;3-(HydroxyMethyl)-1H-inda...;3-HYDROXYMETHYL (1H)INDAZOLE
CBNumber
CB4246121
Molecular Formula
C8H8N2O
Formula Weight
148.16
MOL File
64132-13-4.mol
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3-(HYDROXYMETHYL)INDAZOLE Property

Melting point:
138-139 °C
Boiling point:
380.3±17.0 °C(Predicted)
Density 
1.360±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
form 
solid
pka
13.56±0.10(Predicted)
color 
White
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Safety

HS Code 
2933998090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
I628078
Product name
(1H-Indazol-3-yl)methanol
Packaging
100mg
Price
$75
Updated
2021/12/16
Matrix Scientific
Product number
075035
Product name
3-(Hydroxymethyl)indazole
Purity
95+%
Packaging
5g
Price
$230
Updated
2021/12/16
Matrix Scientific
Product number
075035
Product name
3-(Hydroxymethyl)indazole
Purity
95+%
Packaging
10g
Price
$324
Updated
2021/12/16
SynQuest Laboratories
Product number
4H56-1-LR
Product name
3-(Hydroxymethyl)-1H-indazole
Packaging
5G
Price
$410
Updated
2021/12/16
AK Scientific
Product number
W7591
Product name
(1H-Indazol-3-yl)methanol
Packaging
10g
Price
$487
Updated
2021/12/16
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3-(HYDROXYMETHYL)INDAZOLE Chemical Properties,Usage,Production

Synthesis

4498-67-3

64132-13-4

The general procedure for the synthesis of 3-hydroxymethylindazole from indazole-3-carboxylic acid is as follows: 1. Synthesis of (1H-indazol-3-yl)methanol [Compound (I)]: indazole-3-carboxylic acid (500 mg, 3.08 mmol) was dissolved in tetrahydrofuran (THF, 10 mL) and sodium bis(2-methoxyethoxy)aluminum hydride (70% toluene solution, 1.78 g, 6.17 mmol) was added. It was cooled in an ice bath under argon protection and subsequently heated and stirred at reflux for 2 hours. 2. Cooled in an ice bath again, added sodium bis(2-methoxyethoxy)aluminum hydride (70% toluene solution, 2.67 g, 9.25 mmol) to the reaction mixture and continued to heat and reflux for 2 hours. 3. After completion of the reaction, the ice bath was cooled, 2 mol/L sodium hydroxide solution (10 mL) was added and stirred for 15 minutes at room temperature. 4. The organic layer was separated and the aqueous layer was extracted with THF (5 mL × 3). Combine the organic layers and wash with saturated brine. 5. The aqueous layer was then extracted with ethyl acetate (5 mL × 2), all organic layers were combined, dried with anhydrous magnesium sulfate, and concentrated under reduced pressure. 6. The residue was recrystallized with toluene/THF (10:1, 5 mL), the precipitated crystals were collected by filtration and washed with toluene/THF (10:1, 1 mL). 7. The resulting crystals were dried under pressure to give compound (I) (349 mg, 2.36 mmol, 77% yield). Characterization data: 1H-NMR (DMSO-d6, ppm): δ 4.80 (2H, d, J = 5.5 Hz), 5.19 (1H, br), 7.09 (1H, t, J ≈ 8 Hz), 7.33 (1H, t, J ≈ 8 Hz), 7.48 (1H, d, J = 8.4 Hz), 7.85 (1H, d, J = 8.4 Hz). 13C-NMR (DMSO-d6, ppm): δ 56.7, 109.9, 119.6, 120.5, 121.4, 125.8, 140.9, 145.5. Mass Spectrometry (C8H9N2O): Calculated [M + H]+: 149.0715, measured: 149.0710 (error: -0.5 mDa). Melting point: 142-143°C.

References

[1] Patent: EP1878737, 2008, A1. Location in patent: Page/Page column 12
[2] Patent: WO2005/9958, 2005, A1. Location in patent: Page 100-101
[3] Patent: US2006/142247, 2006, A1. Location in patent: Page/Page column 28
[4] Angewandte Chemie - International Edition, 2014, vol. 53, # 28, p. 7259 - 7263
[5] Angew. Chem., 2014, vol. 126, # 28, p. 7387 - 7391,5

3-(HYDROXYMETHYL)INDAZOLE Preparation Products And Raw materials

Raw materials

Preparation Products

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