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(+)-3-Bromocamphor

(+)-3-Bromocamphor structure

(+)-3-Bromocamphor 

structure
  • CAS No:

    10293-06-8

  • Formula:

    C10H15BrO

  • Chemical Name:

    (+)-3-Bromocamphor

  • Synonyms:

    Bicyclo[2.2.1]heptan-2-one,3-bromo-1,7,7-trimethyl-,(1R,3S,4S)-;2-Bornanone,3-bromo-,(1R,3S,4S)-(+)-;Bicyclo[2.2.1]heptan-2-one,3-bromo-1,7,7-trimethyl-,(1R-endo)-;Camphor,3α-bromo-,(+)-;(1R,3S,4S)-3-Bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one;endo-(+)-3-Bromo-2-bornanone;(+)-3-Bromocamphor;(+)-endo-3-Bromocamphor;(1R-endo)-(+)-3-Bromocamphor;(1R)-endo-3-Bromocamphor;(1R-endo)-3-Bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one

  • Categories:

    Organic Chemistry  >  Phosphines

(+)-3-Bromocamphor Basic Attributes

231.13

231.13

233-652-1

2914700090

Characteristics

17.07000

2.42

White Crystalline

1.4±0.1 g/cm3

76 °C

274 °C

35.8±9.9 °C

1.529

2-8°C

0.028mmHg at 25°C

130 º (c=5, CH3OH)

Safety Information

NONH for all modes of transport

3

36/37/38

26-36-37/39

ED6750000

Xi

Stable under normal temperatures and pressures.

P261-P305 + P351 + P338

H315-H319-H335

(+)-3-Bromocamphor Use and Manufacturing

Methods of Manufacturing

Put camphor and a small amount of chloroform into the reaction pot, slowly add bromine below 90°C. After the addition, the temperature is increased to 115°C and kept at 115-130°C for nearly 3h. cool down. Crush to obtain α-bromocamphor.

Uses

Used as organic synthesis intermediate, pharmaceutical intermediate, and chiral structural unit

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