2-(Benzo[d][1,3]dioxol-5-yl)ethanol
- Product Name
- 2-(Benzo[d][1,3]dioxol-5-yl)ethanol
- CAS No.
- 6006-82-2
- Chemical Name
- 2-(Benzo[d][1,3]dioxol-5-yl)ethanol
- Synonyms
- Homopiperonyl alcohol;1,3-Benzodioxole-5-ethanol;2-(1,3-BENZODIOXOL-5-YL)ETHANOL;3,4-METHYLENEDIOXYPHENYL-1-ETHANOL;5-(2-Hydroxyethyl)-1,3-benzodioxole;2-(1,3-Benzodioxol-5-yl)ethanol 97%;2-(3,4-Methylenedioxyphenyl)ethanol;2-(benzo[d][1,3]dioxol-5-yl)ethanol;2-(2H-1,3-Benzodioxol-5-yl)ethan-1-ol;3,4-(METHYLENEDIOXY)PHENETHYL ALCOHOL
- CBNumber
- CB2688462
- Molecular Formula
- C9H10O3
- Formula Weight
- 166.17
- MOL File
- 6006-82-2.mol
2-(Benzo[d][1,3]dioxol-5-yl)ethanol Property
- Boiling point:
- 115-117
- Density
- 1.269±0.06 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,Room Temperature
- pka
- 14.87±0.10(Predicted)
- Appearance
- Light yellow to yellow Liquid
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Danger
- Hazard statements
-
H302Harmful if swallowed
H312Harmful in contact with skin
H314Causes severe skin burns and eye damage
H332Harmful if inhaled
- Precautionary statements
-
P260Do not breathe dust/fume/gas/mist/vapours/spray.
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P271Use only outdoors or in a well-ventilated area.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P301+P330+P331IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.
P302+P352IF ON SKIN: wash with plenty of soap and water.
P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P310Immediately call a POISON CENTER or doctor/physician.
P312Call a POISON CENTER or doctor/physician if you feel unwell.
P321Specific treatment (see … on this label).
P322Specific measures (see …on this label).
P330Rinse mouth.
P363Wash contaminated clothing before reuse.
P405Store locked up.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- B115013
- Product name
- 2-(2H-1,3-benzodioxol-5-yl)ethan-1-ol
- Packaging
- 10mg
- Price
- $45
- Updated
- 2021/12/16
- Product number
- 064063
- Product name
- 2-(2H-1,3-Benzodioxol-5-yl)ethan-1-ol
- Purity
- 95+%
- Packaging
- 500mg
- Price
- $262
- Updated
- 2021/12/16
- Product number
- 064063
- Product name
- 2-(2H-1,3-Benzodioxol-5-yl)ethan-1-ol
- Purity
- 95+%
- Packaging
- 1g
- Price
- $328
- Updated
- 2021/12/16
- Product number
- 6478AE
- Product name
- 2-(2H-1,3-Benzodioxol-5-yl)ethan-1-ol
- Packaging
- 2.5g
- Price
- $714
- Updated
- 2021/12/16
- Product number
- CHM0018474
- Product name
- 2-(1,3-BENZODIOXOL-5-YL)ETHANOL
- Purity
- 95.00%
- Packaging
- 500MG
- Price
- $720.84
- Updated
- 2021/12/16
2-(Benzo[d][1,3]dioxol-5-yl)ethanol Chemical Properties,Usage,Production
Synthesis
2861-28-1
6006-82-2
6.2.1 Synthesis of 2-(1,3-benzodioxol-5-yl)ethanol (21) [9]. A solution of anhydrous THF (10 mL) with acid 20 (3.00 mmol) was slowly added dropwise to a suspension of anhydrous THF (20 mL) with lithium aluminum hydride (0.114 g, 3.00 mmol) over 15 min. After 4 h of reaction, methanol (1 mL) and 10% NaOH aqueous solution (2 mL) were added sequentially to quench the excess reducing agent until aluminum hydroxide precipitate was formed. Subsequently, the reaction mixture was neutralized with 10% aqueous hydrochloric acid solution (about 5 mL). The resulting mixture was extracted with ethyl acetate (3 x 15 mL), and the combined organic phases were washed with brine, concentrated under reduced pressure, and dried over anhydrous sodium sulfate. The residue was purified by silica gel column chromatography (eluent: CHCl3/EtOH = 100:1) to afford the target product, sterol 21, as a yellow oil in a yield of 0.489 g (98%). Thin layer chromatography (TLC) Rf = 0.5 (CHCl3/EtOH = 20:1). IR (thin film, cm-1): 3351, 2883, 1607, 1503, 1489, 1442, 1247, 1040. 1H NMR (CDCl3): δ 1.87 (br, 1H, ArCH2CH2OH); 2.76 (t, J = 6.5 Hz, 2H, ArCH2CH2OH); 3.78 (t, J = 6.5 Hz, 2H, ArCH2CH2OH); 5.91 (s, 2H, OCH2O); 6.65 (dd, J = 7.8 Hz, J = 1.6 Hz, 1H, 4'); 6.71-6.70 (m, 1H, 2'); 6.75 (d, J = 7.8 Hz, 1H, 5').13C NMR (CDCl3): δ 38.6 (ArCH2CH2OH); 63.5 (ArCH2CH2OH); 100.6 (OCH2O); 108.1 (CH, 2'); 109.1 (CH, 5'); 121.7 (CH, 6'); 132.0 (C, 1'); 145.9 (CH, 4'); 147.5 (CH, 3').
References
[1] Journal of Medicinal Chemistry, 1993, vol. 36, # 22, p. 3333 - 3340
[2] Patent: US6342610, 2002, B2. Location in patent: Page column 121
[3] European Journal of Medicinal Chemistry, 2016, vol. 122, p. 601 - 610
[4] Tetrahedron Letters, 1997, vol. 38, # 25, p. 4347 - 4350
[5] Journal of Medicinal Chemistry, 2005, vol. 48, # 14, p. 4618 - 4627
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