2-ISO-PROPYLBENZALDEHYDE
- Product Name
- 2-ISO-PROPYLBENZALDEHYDE
- CAS No.
- 6502-22-3
- Chemical Name
- 2-ISO-PROPYLBENZALDEHYDE
- Synonyms
- 2-ISO-PROPYLBENZALDEHYDE;2-(propan-2-yl)benzaldehyde;Benzaldehyde,2-(1-Methylethyl)-
- CBNumber
- CB6707776
- Molecular Formula
- C10H12O
- Formula Weight
- 148.2
- MOL File
- 6502-22-3.mol
2-ISO-PROPYLBENZALDEHYDE Property
- Boiling point:
- 104°C/12.2mm
- Density
- 0.980
- Flash point:
- 91℃
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- solid
- Appearance
- Colorless to light yellow Liquid
- InChI
- InChI=1S/C10H12O/c1-8(2)10-6-4-3-5-9(10)7-11/h3-8H,1-2H3
- InChIKey
- DTALCVXXATYTQJ-UHFFFAOYSA-N
- SMILES
- C(=O)C1=CC=CC=C1C(C)C
Safety
- Hazard Codes
- Xi
- Risk Statements
- 37/38-41-51
- Safety Statements
- 26-39
- HS Code
- 2912290090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
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.
N-Bromosuccinimide Price
- Product number
- I874660
- Product name
- 2-Isopropylbenzaldehyde
- Packaging
- 50mg
- Price
- $45
- Updated
- 2021/12/16
- Product number
- OR939813
- Product name
- 2-Isopropylbenzaldehyde
- Purity
- 95%
- Packaging
- 1g
- Price
- $254
- Updated
- 2021/12/16
- Product number
- OR939813
- Product name
- 2-Isopropylbenzaldehyde
- Purity
- 95%
- Packaging
- 250mg
- Price
- $145
- Updated
- 2021/12/16
- Product number
- 143251
- Product name
- 2-Isopropylbenzaldehyde
- Purity
- 97%
- Packaging
- 1g
- Price
- $388
- Updated
- 2021/12/16
- Product number
- OR939813
- Product name
- 2-Isopropylbenzaldehyde
- Purity
- 95%
- Packaging
- 5g
- Price
- $696
- Updated
- 2021/12/16
2-ISO-PROPYLBENZALDEHYDE Chemical Properties,Usage,Production
Synthesis
7073-94-1
68-12-2
6502-22-3
GENERAL STEPS: n-Butyllithium (2.5 M hexane solution, 858 μL, 2.14 mmol) was added slowly and dropwise to an anhydrous tetrahydrofuran (THF) solution of 1-bromo-2-isopropylbenzene (388 mg, 298 μL, 1.95 mmol) at -78 °C. After maintaining the reaction temperature at -78 °C for 20 min, N,N-dimethylformamide (157 mg, 166 μL, 2.14 mmol) was added and stirring was continued at -78 °C for 20 min, followed by slow warming of the reaction mixture to -10 °C and stirring for 3 h at this temperature. Upon completion of the reaction, the reaction was quenched by the addition of water (2.5 mL) and extracted with ether (3 × 100 mL). The organic layers were combined, dried with anhydrous magnesium sulfate (MgSO?), filtered and concentrated under reduced pressure to afford 2-isopropylbenzaldehyde (277 mg, quantitative yield) as a colorless oil. The structure of the product was confirmed by spectroscopic data (Ewing, 1974) and it could be used in subsequent reactions without further purification.
References
[1] Neuropharmacology, 2015, vol. 95, p. 503 - 510
[2] Chemistry Letters, 2007, vol. 36, # 1, p. 72 - 73
[3] Canadian Journal of Chemistry, 1991, vol. 69, # 6, p. 919 - 926
[4] Journal of Organic Chemistry, 2008, vol. 73, # 7, p. 2811 - 2818
[5] Journal of the American Chemical Society, 2008, vol. 130, # 26, p. 8481 - 8490
2-ISO-PROPYLBENZALDEHYDE Preparation Products And Raw materials
Raw materials
Preparation Products
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