2-BROMO-5-HYDROXYBENZALDEHYDE CAS 2973-80-0

Introduction:Basic information about 2-BROMO-5-HYDROXYBENZALDEHYDE CAS 2973-80-0, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

2-BROMO-5-HYDROXYBENZALDEHYDE Basic information

Product Name:2-BROMO-5-HYDROXYBENZALDEHYDE
Synonyms:2-BroMo-5-hydroxybenzaldehyde, 98%+;Benzaldehyde, 2-bromo-5-hydroxy-;2-Bromo-5-hydroxybenzaldehyde 95%;4-BROMO-3-FORMYLPHENOL;AKOS B020430;2-BROMO-5-HYDROXYBENZALDEHYDE;ART-CHEM-BB B020430;2-Bromo-5-(Hydroxyl)Benzaldehyde
CAS:2973-80-0
MF:C7H5BrO2
MW:201.02
EINECS:
Product Categories:API intermediates;Aryl;Halogenated;Organohalides
Mol File:2973-80-0.mol

2-BROMO-5-HYDROXYBENZALDEHYDE Chemical Properties

Melting point 130-135 °C
Boiling point 286.7±20.0 °C(Predicted)
density 1.737±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,2-8°C
solubility Soluble in chloroform, dichloromethane and ethyl acetate.
form Solid
pka8.67±0.18(Predicted)
color White to Gray to Brown
InChIInChI=1S/C7H5BrO2/c8-7-2-1-6(10)3-5(7)4-9/h1-4,10H
InChIKeySCRQAWQJSSKCFN-UHFFFAOYSA-N
SMILESC(=O)C1=CC(O)=CC=C1Br
CAS DataBase Reference2973-80-0(CAS DataBase Reference)

Safety Information

Hazard Codes Xi,N,Xn
Risk Statements 36/37/38-50-22
Safety Statements 26-36/37/39-61
RIDADR UN 3077
WGK Germany 3
Hazard Note Irritant
HazardClass 9
PackingGroup III
HS Code 2909500090
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Aquatic Acute 1

2-BROMO-5-HYDROXYBENZALDEHYDE Usage And Synthesis

Chemical PropertiesPale Grey Solid
Uses2-Bromo-5-hydroxybenzadehyde is a reactant used in the preparation of many pharmaceutical agents: Bcl-XL, PDE4 inhibitors, inhibitors of prostate cancer cell growth and anti-inflamatory agents.
Uses2-Bromo-5-hydroxybenzaldehyde is a useful reactant used in the synthesis of PDE4 inhibitors, BCL-XL and cancel cell growth inhibitors. Also an reactant used in the preparation of many pharmaceutical agents.
Synthesis

100-83-4

2973-80-0

General procedure for the synthesis of 2-bromo-5-hydroxybenzaldehyde from m-hydroxybenzaldehyde: 3-hydroxybenzaldehyde (120 g, 0.98 mol) was suspended in 2400 mL of dichloromethane (CH2Cl2) in a 5 L four-necked, round-bottomed flask fitted with an overhead stirrer, a temperature probe, a dosing funnel, and a condenser tube. The mixture was heated to 35-40 °C to completely dissolve the raw material. Bromine (52 mL, 1.0 mol, 1.02 eq.) was added slowly dropwise through the addition funnel, controlling the rate of dropwise acceleration to maintain the reaction temperature between 35-38°C. After dropwise addition, the reaction mixture was stirred at 35 °C overnight. Subsequently, the mixture was slowly cooled to -5-0 °C over a period of 2 h and stirring was continued for 1 h at this temperature. The precipitated solid was collected by filtration through a Brinell funnel and the filter cake was washed with 400 mL of cold 1:1 n-heptane/dichloromethane mixture. The resulting gray solid was dried under vacuum at room temperature (0.2 mmHg). The yield was 124.3 g in 63% yield.

References[1] Bioorganic and Medicinal Chemistry Letters, 2001, vol. 11, # 8, p. 955 - 959
[2] Patent: US2004/19018, 2004, A1. Location in patent: Page/Page column Sheet 2
[3] Journal of the Iranian Chemical Society, 2011, vol. 8, # 2, p. 531 - 536
[4] Tetrahedron Letters, 2009, vol. 50, # 9, p. 1007 - 1009
[5] Synthetic Communications, 2007, vol. 37, # 4, p. 581 - 585

2-BROMO-5-HYDROXYBENZALDEHYDE Preparation Products And Raw materials

Raw materials2,4-Dibromo-5-hydroxybenzaldehyde-->4-BROMO-3-HYDROXYBENZALDEHYDE-->3-Hydroxy-4-nitrobenzaldehyde-->2-Bromo-5-methoxybenzaldehyde-->2-Bromo-3-hydroxybenzaldehyde-->Dichloromethane-->3-Hydroxybenzaldehyde
Preparation Products2-Bromo-5-methoxybenzaldehyde-->4-Bromo-3-methylphenol-->4-(4-Bromo-3-formyl-phenoxy)-benzonitrile
2-Bromo-5-fluorophenol CAS 147460-41-1
2-Bromo-5-methoxybenzonitrile CAS 138642-47-4
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