| Identification | More | [Name]
4-N-OCTYLOXYBENZALDEHYDE | [CAS]
24083-13-4 | [Synonyms]
4-N-OCTYLOXYBENZALDEHYDE
4-OCTYLOXYBENZALDEHYDE
P-OCTYLOXYBENZALDEHYDE
TIMTEC-BB SBB008008
4-(octyloxy)-benzaldehyd
p-n-Octoxy benzaldehyde
p-n-Octyloxybenzaldehyde
4-n-Octyloxybenzaldehyde,97%
Benzaldehyde, 4-(octyloxy)-
4-N-OCTYLOXYBENZALDEHYDE 98+% | [EINECS(EC#)]
246-012-1 | [Molecular Formula]
C15H22O2 | [MDL Number]
MFCD00014136 | [Molecular Weight]
234.33 | [MOL File]
24083-13-4.mol |
| Chemical Properties | Back Directory | [Appearance]
CLEAR COLOURLESS TO YELLOWISH LIQUID | [Boiling point ]
140-142 °C (0.1 mmHg) | [density ]
0.98
| [refractive index ]
1.52-1.522
| [Fp ]
140-142°C/0.1mm | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [form ]
clear liquid | [color ]
Colorless to Yellow to Green | [Specific Gravity]
0.98 | [Sensitive ]
Air Sensitive | [BRN ]
1913284 | [InChI]
InChI=1S/C15H22O2/c1-2-3-4-5-6-7-12-17-15-10-8-14(13-16)9-11-15/h8-11,13H,2-7,12H2,1H3 | [InChIKey]
KVOWZHASDIKNFK-UHFFFAOYSA-N | [SMILES]
C(=O)C1=CC=C(OCCCCCCCC)C=C1 | [CAS DataBase Reference]
24083-13-4(CAS DataBase Reference) | [EPA Substance Registry System]
Benzaldehyde, 4-(octyloxy)- (24083-13-4) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S37/39:Wear suitable gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . | [TSCA ]
Yes | [HazardClass ]
IRRITANT | [HS Code ]
29130000 |
| Hazard Information | Back Directory | [Chemical Properties]
CLEAR COLOURLESS TO YELLOWISH LIQUID | [Synthesis]
General procedure for the synthesis of 4-n-octyloxybenzaldehyde from 1-bromooctane and p-hydroxybenzaldehyde: In a dry two-necked flask with a magnetic stirrer, 2.44 g (20 mmol) of p-hydroxybenzaldehyde, 19.31 g (100 mmol) of 1-bromooctane, 13.82 g of potassium carbonate and 50 ml of anhydrous acetone were added in sequence. The reaction was magnetically stirred at 80°C for 24 hours. After completion of the reaction, the reaction mixture was extracted several times with water and dichloromethane and the organic phases were combined. After purification by column chromatography, 4.68 g (about 99% yield) of the light yellow liquid product 4-n-octyloxybenzaldehyde was obtained. | [References]
[1] Journal of the Brazilian Chemical Society, 2015, vol. 26, # 3, p. 562 - 571
[2] Patent: CN108102408, 2018, A. Location in patent: Paragraph 0036-0039
[3] Patent: CN108503658, 2018, A. Location in patent: Paragraph 0032; 0033; 0036; 0037
[4] European Journal of Organic Chemistry, 2006, # 19, p. 4379 - 4384
[5] European Journal of Organic Chemistry, 2004, # 18, p. 3865 - 3871 |
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