ChemicalBook > CAS DataBase List > 4-CYCLOPROPYLBENZALDEHYDE

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
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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
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Safety

HS Code 
2902900000
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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.

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N-Bromosuccinimide Price

TRC
Product number
B426000
Product name
4-cyclopropylbenzaldehyde
Packaging
100mg
Price
$200
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC151398
Product name
4-Cyclopropyl-benzaldehyde
Packaging
250mg
Price
$200
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC151398
Product name
4-Cyclopropyl-benzaldehyde
Packaging
50mg
Price
$75
Updated
2021/12/16
Biosynth Carbosynth
Product number
FC151398
Product name
4-Cyclopropyl-benzaldehyde
Packaging
100mg
Price
$120
Updated
2021/12/16
AK Scientific
Product number
9503AJ
Product name
4-Cyclopropylbenzaldehyde
Packaging
100mg
Price
$131
Updated
2021/12/16
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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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4-CYCLOPROPYLBENZALDEHYDE Suppliers

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