ChemicalBook >> CAS DataBase List >>7-Bromo-2,2-dimethylchroman-4-one

7-Bromo-2,2-dimethylchroman-4-one

CAS No.
130200-01-0
Chemical Name:
7-Bromo-2,2-dimethylchroman-4-one
Synonyms
7-Bromo-2,2-dimethylchroman-4-one;7-Bromo-2,2-dimethyl-3H-chromen-4-one;7-BROMO-2,3-DIHYDRO-2,2-DIMETHYLCHROMEN-4-ONE;4H-1-Benzopyran-4-one, 7-bromo-2,3-dihydro-2,2-dimethyl-
CBNumber:
CB73070722
Molecular Formula:
C11H11BrO2
Molecular Weight:
255.11
MDL Number:
MFCD13190381
MOL File:
130200-01-0.mol
MSDS File:
SDS
Last updated:2026-05-28 03:09:52

7-Bromo-2,2-dimethylchroman-4-one Properties

Boiling point 332.7±42.0 °C(Predicted)
Density 1.429±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
Appearance White to light yellow Solid

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338

7-Bromo-2,2-dimethylchroman-4-one price More Price(34)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth FFA20001 7-Bromo-2,2-dimethylchroman-4-one 130200-01-0 5g $413 2026-06-04 Buy
Matrix Scientific 302008 7-Bromo-2,2-dimethylchroman-4-one 130200-01-0 250.00mg $50 2026-05-19 Buy
Matrix Scientific 302008 7-Bromo-2,2-dimethylchroman-4-one 130200-01-0 1.00g $63 2026-05-19 Buy
Matrix Scientific 302008 7-Bromo-2,2-dimethylchroman-4-one 130200-01-0 5.00g $276 2026-05-19 Buy
Synthonix B54449 7-Bromo-2,2-dimethylchroman-4-one 97% 130200-01-0 100mg $46 2026-05-06 Buy
Product number Packaging Price Buy
FFA20001 5g $413 Buy
302008 250.00mg $50 Buy
302008 1.00g $63 Buy
302008 5.00g $276 Buy
B54449 100mg $46 Buy

7-Bromo-2,2-dimethylchroman-4-one Chemical Properties,Uses,Production

Synthesis

3-Bromophenol

591-20-8

7-Bromo-2,2-dimethylchroman-4-one

130200-01-0

General procedure for the synthesis of 7-bromo-2,2-dimethylchromen-4-one from m-bromophenol: About 15 g of polyphosphoric acid was added to a mixture of 3,3-dimethylacrylic acid (5.0 g, 54.9 mmol) and 3-bromophenol (10.4 g, 60.4 mmol). The mixture was stirred and reacted at 95 °C for 4 h under argon protection. Upon completion of the reaction, the reaction slurry was cooled to 0 °C with an ice bath, dissolved in 200 mL of ice water and subsequently extracted with ether (3 x 100 mL). The organic phase was separated and washed sequentially with 5N KOH aqueous solution (50 mL) and saturated saline (50 mL). The extract was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (eluent: 5% ethyl acetate/hexane) to afford 7-bromo-2,2-dimethylchromen-4-one (2.80 g, 22% yield) as a brown solid.1H-NMR (300 MHz, CDCl3) data were as follows: δ 1.45 (s, 6H), 2.71 (s, 2H), 7.13 (m, 2H), and 7.72 (d, 1H, J = 8.3 Hz).

References

[1] Patent: US6403638, 2002, B1

30186-18-6
67-64-1
130200-01-0
Synthesis of 7-Bromo-2,2-dimethylchroman-4-one from 4-Bromo-2-hydroxyacetophenone and Acetone

7-Bromo-2,2-dimethylchroman-4-one Preparation Products And Raw materials

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7-Bromo-2,2-dimethylchroman-4-one Spectrum

7-Bromo-2,2-dimethylchroman-4-one 7-BROMO-2,3-DIHYDRO-2,2-DIMETHYLCHROMEN-4-ONE 7-Bromo-2,2-dimethyl-3H-chromen-4-one 4H-1-Benzopyran-4-one, 7-bromo-2,3-dihydro-2,2-dimethyl- 130200-01-0