Quinolin-3-yl-methanol
- Product Name
- Quinolin-3-yl-methanol
- CAS No.
- 13669-51-7
- Chemical Name
- Quinolin-3-yl-methanol
- Synonyms
- 3-quinolylmethanol;3-Quinolinylmethanol;Quinolin-3-yl-methanol;3-(hydroxyMethyl)quinoline
- CBNumber
- CB91180490
- Molecular Formula
- C10H9NO
- Formula Weight
- 159.18
- MOL File
- 13669-51-7.mol
Quinolin-3-yl-methanol Property
- storage temp.
- Sealed in dry,Room Temperature
- Boiling point:
- 329.8±17.0 °C(Predicted)
- Density
- 1.218±0.06 g/cm3(Predicted)
- Melting point:
- 65-67 °C
- pka
- 13.68±0.10(Predicted)
- Appearance
- Off-white to light yellow Solid
Safety
- HazardClass
- IRRITANT
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H320Causes eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P302+P352IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- E592320
- Product name
- Quinolin-3-ylmethanol
- Packaging
- 500mg
- Price
- $350
- Updated
- 2021/12/16
- Product number
- 062383
- Product name
- Quinolin-3-ylmethanol
- Packaging
- 5g
- Price
- $798
- Updated
- 2021/12/16
- Product number
- CHM0117363
- Product name
- 3-QUINOLINEMETHANOL
- Purity
- 95.00%
- Packaging
- 1G
- Price
- $1070.84
- Updated
- 2021/12/16
- Product number
- CHM0117363
- Product name
- 3-QUINOLINEMETHANOL
- Purity
- 95.00%
- Packaging
- 2.5G
- Price
- $1635.3
- Updated
- 2021/12/16
- Product number
- CHM0117363
- Product name
- 3-QUINOLINEMETHANOL
- Purity
- 95.00%
- Packaging
- 5G
- Price
- $2181.31
- Updated
- 2021/12/16
Quinolin-3-yl-methanol Chemical Properties,Usage,Production
Synthesis
13669-42-6
13669-51-7
Step 1: Sodium borohydride (240 mg, 6.4 mmol) was added batchwise to a solution of quinoline-3-carbaldehyde (910 mg, 5.8 mmol) in methanol (10 mL) at room temperature. The reaction mixture was stirred for 3 hours and then the reaction was quenched with saturated aqueous ammonium chloride solution (10 mL). Subsequently, the reaction mixture was extracted with ethyl acetate (3 x 30 mL). The organic phases were combined, washed with brine and dried with anhydrous magnesium sulfate. After filtration, the filtrate was concentrated under reduced pressure to afford the crude quinolin-3-ylmethanol (795 mg, 86% yield).
References
[1] Journal of Organic Chemistry, 1990, vol. 55, # 19, p. 5344 - 5347
[2] European Journal of Organic Chemistry, 2009, # 26, p. 4458 - 4467
[3] Patent: WO2008/115516, 2008, A2. Location in patent: Page/Page column 65
[4] Patent: WO2005/123724, 2005, A1. Location in patent: Page/Page column 73
[5] Heterocycles, 1999, vol. 51, # 8, p. 1883 - 1889
Quinolin-3-yl-methanol Preparation Products And Raw materials
Raw materials
Preparation Products
Quinolin-3-yl-methanol Suppliers
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