6-Bromo-1-hexanol

6-Bromo-1-hexanol
  • CAS No.:4286-55-9
Other grades of this product :
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
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.)
Fp >230 °F
storage temp. 2-8°C
solubility Soluble in chloroform and methanol.
pka15.16±0.10(Predicted)
form Oil
color Clear Colorless
BRN 1732415
Stability:Stable. Incompatible with strong oxidizing agents, acid chlorides, acid anhydrides.
InChIKeyFCMCSZXRVWDVAW-UHFFFAOYSA-N
LogP2.16 at 25℃
CAS DataBase Reference4286-55-9(CAS DataBase Reference)
EPA Substance Registry System1-Hexanol, 6-bromo- (4286-55-9)
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 Information
ProviderLanguage
1-Bromo-6-hydroxyhexane English
ACROS English
SigmaAldrich English
ALFA English
6-Bromo-1-hexanol Usage And Synthesis
Chemical Propertiescolourless or light yellow liquid
UsesA product for proteomics research
UsesA 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.
Uses6-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/ja01167a091Synthesis, p. 1161, 1985 DOI: 10.1055/s-1985-31464Tetrahedron Letters, 36, p. 711, 1995 DOI: 10.1016/0040-4039(94)02340-H
6-Bromo-1-hexanol Preparation Products And Raw materials
Preparation Products(5-Carboxypentyl)(triphenyl)phosphonium bromide-->6-bromohexan-1-amine-->7-HYDROXYHEPTANOIC ACID-->1-Bromo-6-chlorohexane-->6-Mercaptohexan-1-ol

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