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5-Bromo-3-methoxysalicylaldehyde

5-Bromo-3-methoxysalicylaldehyde

CAS: 5034-74-2

Molecular Formula: C8H7BrO3

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5-Bromo-3-methoxysalicylaldehyde - Names and Identifiers

Name 5-Bromo-3-methoxysalicylaldehyde
Synonyms 5-BROMO-O-VANILLIN
5-BROMO-2-VANILLIN
OTAVA-BB BB7018802005
5-Bromo-3-methoxysalicylaldehyde
5-BROMO-3-METHOXYSALICYLALDEHYDE
5-bromo-2-hydroxy-3-methoxybenzaldehyde
5-BROMO-2-HYDROXY-3-METHOXYBENZALDEHYDE
benzaldehyde, 5-bromo-2-hydroxy-3-methoxy-
5-BROMO-2-HYDROXY-3-METHOXYBENZENECARBALDEHYDE
CAS 5034-74-2
EINECS 628-660-0
InChI InChI=1/C8H7BrO3/c1-12-7-3-6(9)2-5(4-10)8(7)11/h2-4,11H,1H3

5-Bromo-3-methoxysalicylaldehyde - Physico-chemical Properties

Molecular FormulaC8H7BrO3
Molar Mass231.04
Density1.6494 (rough estimate)
Melting Point125-127 °C (lit.)
Boling Point277.2±35.0 °C(Predicted)
Flash Point121.4°C
Vapor Presure0.00272mmHg at 25°C
BRN2328601
pKa7.62±0.23(Predicted)
Storage Conditionunder inert gas (nitrogen or Argon) at 2-8°C
SensitiveAir Sensitive
Refractive Index1.4730 (estimate)

5-Bromo-3-methoxysalicylaldehyde - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk Codes36/37/38 - Irritating to eyes, respiratory system and skin.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S37/39 - Wear suitable gloves and eye/face protection
WGK Germany3
HS Code29130000

5-Bromo-3-methoxysalicylaldehyde - Introduction

It is an organic compound with the chemical formula C8H7BrO3.

Nature:
-Appearance: Colorless crystalline solid.
-Melting point: about 128-130 degrees Celsius.
-Boiling point and fire point data are not reported.
-Solubility: Soluble in most organic solvents, such as ethanol, acetone and dichloromethane.

Use:
-As an intermediate for the synthesis and adjustment of organic photoelectric functional materials.
-has applications in the synthesis of drugs, dyes and pigments.

Preparation Method:
It can be prepared by the following steps:
1. The benzaldehyde substituted at the 3-position reacts with bromo methanol to generate 3-methoxybenzaldehyde.
2. Under alkaline conditions, 3-methoxybenzaldehyde reacts with hydrogen bromide to generate 5-bromo-3-methoxybenzaldehyde.
3. The product obtained by synthesis converts the methoxy moiety into hydroxyl group through reduction or other chemical reactions to obtain the final product.

Safety Information:
-It may be irritating and sensitizing to the human body, and protective measures should be taken when contacting.
-In the use or preparation process should follow the laboratory safety procedures, pay attention to protect the eyes and skin, and ensure that the operation is carried out in a well-ventilated place.
-If exposed or inhaled, seek medical attention immediately.
Last Update:2024-04-09 02:00:46
5-Bromo-3-methoxysalicylaldehyde
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5-Bromo-3-methoxysalicylaldehyde
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