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6-Bromo-1-hexanol

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6-Bromo-1-hexanol Basic information

Product Name:
6-Bromo-1-hexanol
Synonyms:
  • 6-BROMO-1-HEXANOL
  • 6-BROMO-N-HEXANOL
  • 6-BROMO-HEXAN-1-OL
  • 6-BROMOHEXANOL
  • 1-bromo-6-hydroxyhexane
  • 6-Hydroxyhexyl bromide
  • 6-Bromo-1-hexanol,95%
  • 6-Bromo-1-hydroxyhexane, Hexamethylene bromohydrin
CAS:
4286-55-9
MF:
C6H13BrO
MW:
181.07
EINECS:
610-072-0
Product Categories:
  • Pyrimidines
  • OLED materials,pharm chemical,electronic
  • blocks
  • Bromides
  • omega-Bromoalkanols
  • omega-Functional Alkanols, Carboxylic Acids, Amines & Halides
  • Aliphatics
  • Halides
  • bc0001
Mol File:
4286-55-9.mol
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6-Bromo-1-hexanol Chemical Properties

Boiling point:
105-106 °C5 mm Hg(lit.)
Density 
1.384 g/mL at 25 °C(lit.)
vapor pressure 
0.25Pa at 20℃
refractive index 
n20/D 1.482(lit.)
Flash point:
>230 °F
storage temp. 
2-8°C
solubility 
Soluble in chloroform and methanol.
pka
15.16±0.10(Predicted)
form 
Oil
color 
Clear Colorless
BRN 
1732415
Stability:
Stable. Incompatible with strong oxidizing agents, acid chlorides, acid anhydrides.
InChIKey
FCMCSZXRVWDVAW-UHFFFAOYSA-N
LogP
2.16 at 25℃
CAS DataBase Reference
4286-55-9(CAS DataBase Reference)
EPA Substance Registry System
1-Hexanol, 6-bromo- (4286-55-9)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-37/39
WGK Germany 
3
TSCA 
Yes
HS Code 
29055900

MSDS

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6-Bromo-1-hexanol Usage And Synthesis

Chemical Properties

colourless or light yellow liquid

Uses

A product for proteomics research. Also used as a reagent in the preparation of nitric oxide-donating analogues of Sulindac (S699215), a non-steroidal anti-inflammatory drug that has the ability to prevent colon cancer.

Uses

6-Bromo-1-hexanol is a useful synthetic intermediate. 6-Bromo-1-hexanol is used as a reagent in the preparation of nitric oxide-donating analogues of Sulindac (S699215), a non-steroidal anti-inflammatory drug that has the ability to prevent colon cancer.

Synthesis Reference(s)

Journal of the American Chemical Society, 72, p. 5137, 1950 DOI: 10.1021/ja01167a091
Synthesis, p. 1161, 1985 DOI: 10.1055/s-1985-31464
Tetrahedron Letters, 36, p. 711, 1995 DOI: 10.1016/0040-4039(94)02340-H

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