4-CYCLOPROPYLBENZALDEHYDE
- Product Name
- 4-CYCLOPROPYLBENZALDEHYDE
- CAS No.
- 20034-50-8
- Chemical Name
- 4-CYCLOPROPYLBENZALDEHYDE
- Synonyms
- AKOS BAR-1174;4-CYCLOPROPYLBENZALDEHYDE;p-Cyclopropylbenzaldehyde;Benzaldehyde,4-cyclopropyl-
- CBNumber
- CB5312928
- Molecular Formula
- C10H10O
- Formula Weight
- 146.19
- MOL File
- 20034-50-8.mol
4-CYCLOPROPYLBENZALDEHYDE Property
- Boiling point:
- 113 °C
- Density
- 1.0512 g/cm3
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- Appearance
- Colorless to light yellow Liquid
Safety
- HS Code
- 2902900000
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.
P271Use only outdoors or in a well-ventilated area.
P280Wear protective gloves/protective clothing/eye protection/face protection.
N-Bromosuccinimide Price
- Product number
- B426000
- Product name
- 4-cyclopropylbenzaldehyde
- Packaging
- 100mg
- Price
- $200
- Updated
- 2021/12/16
- Product number
- FC151398
- Product name
- 4-Cyclopropyl-benzaldehyde
- Packaging
- 250mg
- Price
- $200
- Updated
- 2021/12/16
- Product number
- FC151398
- Product name
- 4-Cyclopropyl-benzaldehyde
- Packaging
- 50mg
- Price
- $75
- Updated
- 2021/12/16
- Product number
- FC151398
- Product name
- 4-Cyclopropyl-benzaldehyde
- Packaging
- 100mg
- Price
- $120
- Updated
- 2021/12/16
- Product number
- 9503AJ
- Product name
- 4-Cyclopropylbenzaldehyde
- Packaging
- 100mg
- Price
- $131
- Updated
- 2021/12/16
4-CYCLOPROPYLBENZALDEHYDE Chemical Properties,Usage,Production
Synthesis
1122-91-4
411235-57-9
20034-50-8
Using p-bromobenzaldehyde and cyclopropylboronic acid as starting materials, 4-cyclopropylbenzaldehyde was prepared by reacting 6-(4-bromophenyl)-3-((2-chlorophenyl)thio)-6-(thiophen-3-yl)piperidin-2,4-dione with 6-(4-bromophenyl)-3-((2-chlorophenyl)thio)-6-(thiophen-3-yl)piperidin-2,4-dione with reference to the method of Example 8 Step A. The method was carried out by substituting cyclopropylboronic acid as cyclohex-1-en-1-ylboronic acid. After completion of the reaction, the target product was obtained after post-treatment in 80% yield.
References
[1] Synthetic Communications, 2006, vol. 36, # 1, p. 121 - 128
[2] Patent: US2016/31892, 2016, A1. Location in patent: Paragraph 0187-0188
[3] Tetrahedron Letters, 2002, vol. 43, # 39, p. 6987 - 6990
[4] Patent: WO2015/140133, 2015, A1. Location in patent: Page/Page column 137
[5] Patent: WO2013/142269, 2013, A1. Location in patent: Paragraph 0721; 0722; 0723
4-CYCLOPROPYLBENZALDEHYDE Preparation Products And Raw materials
Raw materials
Preparation Products
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