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ChemicalBook >> CAS DataBase List >>2-Bromo-2′-hydroxyacetophenone

2-Bromo-2′-hydroxyacetophenone

CAS No.
2491-36-3
Chemical Name:
2-Bromo-2′-hydroxyacetophenone
Synonyms
2-broMo-1-(2-hydroxyphenyl)ethan-1-one;2-AMINO-3'2-Bromo-2′Cyclohexane Impurity 4;2-HYDROXYPHENACYL BROMIDE;2-BROMO-2'-HYDROXYACETOPHENONE;2-Bromo-2’-hydroxyacetophenone;2-(2-bromoacetyl)hydroxybenzene;2-Bromo-2'-hydroxylacetophenone;2-Bromo-2'-hydroxyacetophenone 97%
CBNumber:
CB6675345
Molecular Formula:
C8H7BrO2
Molecular Weight:
215.04
MDL Number:
MFCD01727570
MOL File:
2491-36-3.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-06-04 16:00:12
Product description Number Pack Size Price
2-Bromo-2′-hydroxyacetophenone 97% 594938 1g $70.5
2-Bromo-2′-hydroxyacetophenone 97% 594938 5g $137
2-Bromo-2'-hydroxyacetophenone B4735 1G $60
2-Bromo-2'-hydroxyacetophenone B4735 5G $181
2-Bromo-2’-hydroxyacetophenone TRC-B684455-500MG 500mg $148

2-Bromo-2′-hydroxyacetophenone Properties

Melting point 44-48 °C(lit.)
Boiling point 152-158 °C(Press: 18 Torr)
Density 1.622±0.06 g/cm3(Predicted)
Flash point >230 °F
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility Chloroform, Methanol
pka 7.63±0.30(Predicted)
form Solid
color Yellow
Sensitive Lachrymatory
InChI 1S/C8H7BrO2/c9-5-8(11)6-3-1-2-4-7(6)10/h1-4,10H,5H2
InChIKey SGPKEYSZPHMVNI-UHFFFAOYSA-N
SMILES Oc1ccccc1C(=O)CBr
CAS DataBase Reference 2491-36-3(CAS DataBase Reference)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
Signal word  Danger
Hazard statements  H302-H314
Precautionary statements  P260-P270-P280-P301+P312-P303+P361+P353-P305+P351+P338
PPE Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  C
Risk Statements  22-34
Safety Statements  26-36/37/39-45
RIDADR  UN 3263 8/PG 2
WGK Germany  3
RTECS  KM5556400
Hazard Note  Corrosive/Lachrymatory/Keep Cold
HazardClass  8
PackingGroup  II
HS Code  29147000
Storage Class 8A - Combustible corrosive hazardous materials
Hazard Classifications Acute Tox. 4 Oral
Skin Corr. 1B
Toxicity mouse,LD50,oral,821mg/kg (821mg/kg),BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX)LUNGS, THORAX, OR RESPIRATION: DYSPNEABEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD,Acute Toxicity Data. Journal of the American College of Toxicology, Part B. Vol. 1, Pg. 183, 1992.
Limited Quantities 1 Kg (2.2 lbs) (solid)
Excepted Quantities Max Inner Pack (30g or 30ml) and Max Outer Pack (500g or 500ml)
NFPA 704
1
3 0

2-Bromo-2′-hydroxyacetophenone price More Price(60)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 594938 2-Bromo-2′-hydroxyacetophenone 97% 2491-36-3 1g $70.5 2022-05-15 Buy
Sigma-Aldrich 594938 2-Bromo-2′-hydroxyacetophenone 97% 2491-36-3 5g $137 2022-05-15 Buy
TCI Chemical B4735 2-Bromo-2'-hydroxyacetophenone 2491-36-3 1G $60 2026-04-30 Buy
TCI Chemical B4735 2-Bromo-2'-hydroxyacetophenone 2491-36-3 5G $181 2026-04-30 Buy
TRC TRC-B684455-500MG 2-Bromo-2’-hydroxyacetophenone 2491-36-3 500mg $148 2026-06-03 Buy
Product number Packaging Price Buy
594938 1g $70.5 Buy
594938 5g $137 Buy
B4735 1G $60 Buy
B4735 5G $181 Buy
TRC-B684455-500MG 500mg $148 Buy

2-Bromo-2′-hydroxyacetophenone Chemical Properties,Uses,Production

Chemical Properties

Off-White Powder

Uses

2-Bromo-2′-hydroxyacetophenone is used as a pharmaceutical intermediate.

Synthesis

2'-Hydroxyacetophenone

118-93-4

2-Bromo-2′-hydroxyacetophenone

2491-36-3

The general procedure for the synthesis of 2-bromo-1-(2-hydroxyphenyl)ethanone from 2'-hydroxyacetophenone is as follows: in a 50 mL round-bottomed flask equipped with a magnetic stirrer, 2'-hydroxyacetophenone (10 mmol) was added. Subsequently, potassium bromide (40 mmol) dissolved in 20 mL of water was added to this solution and mixed with stirring at room temperature. Next, 30% hydrogen peroxide (4 mmol) was slowly added. Vanadium (V) complex (0.01 mmol) and 70% perchloric acid (4 mmol) were further added to the reaction system, and the reaction mixture was stirred at 0°C, followed by raising to room temperature and continued stirring for 10 minutes. Under continuous stirring conditions, additional 70% perchloric acid (4 mmol) was added every 10 min for three times. The reaction process was monitored by thin layer chromatography (TLC). The nuclear magnetic resonance (NMR) spectral data of the final brominated product is detailed in the Supporting Information.

References

[1] Tetrahedron Letters, 2009, vol. 50, # 6, p. 700 - 703
[2] Tetrahedron, 2001, vol. 57, # 11, p. 2203 - 2211
[3] Archiv der Pharmazie, 2009, vol. 342, # 9, p. 541 - 545
[4] Synthetic Communications, 2006, vol. 36, # 19, p. 2877 - 2881
[5] Journal of Organometallic Chemistry, 2018, vol. 876, p. 10 - 16

582-24-1
2491-36-3
Synthesis of 2-Bromo-2′-hydroxyacetophenone from 2-HYDROXYACETOPHENONE

2-Bromo-2′-hydroxyacetophenone Suppliers

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View Lastest Price from 2-Bromo-2′-hydroxyacetophenone manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2-Bromo-2′-hydroxyacetophenone pictures 2026-06-30 2-Bromo-2′-hydroxyacetophenone
2491-36-3
1kg 99% 10000KGS Shaanxi Dideu New Materials Co. Ltd
2-BROMO-2'-HYDROXYACETOPHENONE pictures 2025-04-04 2-BROMO-2'-HYDROXYACETOPHENONE
2491-36-3
1kg 98% 1Ton Henan Aochuang Chemical Co.,Ltd.

2-Bromo-2′-hydroxyacetophenone Spectrum

2-Bromo-2'-hydroxyacetophenone ,97% 2-Bromo-2'-hydroxyacetophenone, 2-Bromo-1-(2-hydroxyphenyl)ethan-1-one, 2-(Bromoacetyl)phenol 2-Bromo-2'-hydroxyacetophenone 97% 2-bromo-1-(2-hydroxyphenyl)-ethanon 2-HYDROXYPHENACYL BROMIDE 2-BROMO-1-(2-HYDROXYPHENYL)ETHANONE 2-BROMO-2'-HYDROXYACETOPHENONE 2-Bromo-2'-hydroxylacetophenone JR-8498, 2-Bromo-1-(2-hydroxyphenyl)ethanone, 97% Ethanone, 2-bromo-1-(2-hydroxyphenyl)- 2-(2-bromoacetyl)hydroxybenzene 2-AMINO-3' 2-Bromo-2’-hydroxyacetophenone 2-Bromo-2′ Cyclohexane Impurity 4 2-broMo-1-(2-hydroxyphenyl)ethan-1-one 2491-36-3 BrCH2COC6H4OH Organic Building Blocks Ketones Building Blocks C7 to C8 Carbonyl Compounds Intermediate of Neticonazole Hydrochloride API intermediates Aromatics C7 to C8 Carbonyl Compounds Ketones
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