ChemicalBook Product Catalog Chemical Reagents Organic reagents Fatty alcohols 11-Bromo-1-undecanol

11-Bromo-1-undecanol

11-Bromo-1-undecanol Basic information
Product Name:11-Bromo-1-undecanol
Synonyms:11-Bromo-1-hydroxyundecane;11-BroMo-1-undecanol puruM, >=99.0% (AT);11-BroMo-1-undecanol, 97% 10GR;11-BroMo-1-undecanol, 97% 50GR;1-Bromo-11-hydroxyundecane;UNDECAMETHYLENE BROMOHYDRIN;11-BROMOUNDECYL ALCOHOL;11-BROMO-1-UNDECANOL
CAS:1611-56-9
MF:C11H23BrO
MW:251.2
EINECS:216-554-3
Product Categories:Alcohols;Building Blocks;C11 to C30+;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds;omega-Bromoalkanols;omega-Functional Alkanols, Carboxylic Acids, Amines & Halides;Linear hydrocarbon series;OLED materials,pharm chemical,electronic
Mol File:1611-56-9.mol
11-Bromo-1-undecanol Structure
11-Bromo-1-undecanol Chemical Properties
Melting point 46-49 °C(lit.)
Boiling point 165-170 °C1 mm Hg(lit.)
density 1.1887 (rough estimate)
refractive index 1.5290 (estimate)
Fp >230 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility chloroform: soluble50mg/mL, clear to slightly hazy, colorless to dark yellow
form Crystals or Crystalline Powder
pka15.20±0.10(Predicted)
color White to beige
Water Solubility Insoluble in water.
BRN 1741180
InChIKeyXFGANBYCJWQYBI-UHFFFAOYSA-N
CAS DataBase Reference1611-56-9(CAS DataBase Reference)
NIST Chemistry Reference1-Undecanol, 11-bromo-(1611-56-9)
Safety Information
Hazard Codes Xn
Risk Statements 20/21/22-36/37/38
Safety Statements 24/25-36-26
WGK Germany 3
HS Code 29055900
MSDS Information
ProviderLanguage
11-Bromo-1-undecanol English
SigmaAldrich English
ACROS English
ALFA English
11-Bromo-1-undecanol Usage And Synthesis
Chemical PropertiesWHITE TO BEIGE CRYSTALS OR CRYSTALLINE POWDER
Uses11-Bromo-1-undecanol was used in the preparation of 11-mercapto-1-undecanol and 1-(2-acryloyloxyundecyl)-3-methylimidazolium bromide. It was used in one-pot synthesis of graft copolymers based on a metathesis skeleton with poly(methyl methacrylate) grafts.
Uses11-Bromo-1-undecanol was used in the preparation of 11-mercapto-1-undecanol and 1-(2-acryloyloxyundecyl)-3-methylimidazolium bromide. It was also used in one-pot synthesis of graft copolymers based on a metathesis skeleton with poly(methyl methacrylate) grafts.
11-Bromo-1-undecanol Preparation Products And Raw materials
Preparation Productstetradec-13-enal-->1-Dodecene,12-broMo--->13-bromotridecanoic acid-->11-AMINO-1-UNDECANOL-->12-methyl-1-tridecanol-->11-MERCAPTOUNDECANOIC ACID-->12-Heptadecyn-1-ol-->1,2-BIS(11-HYDROXYUNDECYLOXY)BENZENE-->4-(11-Acryloyloxyundecyloxy)benzoic acid
5-BETA-PREGNAN-12-ALPHA-BROMO-3-ALPHA, 21-DIOL-11,20-DIONE DIACETATE 16A-BROMOANDROSTERONE 1-(16-BROMO-3,17-DIHYDROXY-10,13-DIMETHYL-2,3,4,7,8,9,10,11,12,13,14,15,16,17-TETRADECAHYDRO-1H-CYCLOPENTA[A]PHENANTHREN-17-YL)ETHAN-1-ONE STIGMASTERYL ACETATE DIBROMIDE 5-ALPHA-ANDROSTAN-2-ALPHA-BROMO-17-BETA-OL-3-ONE 5-ALPHA-ANDROSTAN-2-ALPHA-BROMO-17-ALPHA-METHYL-17-BETA-OL-3-ONE METHYL 11-BROMOUNDECANOATE 16BETA-BROMOANDROSTERONE 3-(ACETYLOXY)-6-BROMO-5-HYDROXY-10,13-DIMETHYLPERHYDROCYCLOPENTA[A]PHENANTHREN-17-YL BENZOATE 5-ALPHA-PREGNAN-16-BETA-BROMO-3-BETA, 17-DIOL-11,20-DIONE 3-ACETATE 5-ALPHA-PREGNAN-21-BROMO-3-BETA, 17-DIOL-11,20-DIONE 11-BROMOUNDECANOIC ACID ETHYL ESTER 16-BROMO-10,13-DIMETHYL-17-OXO-2,3,4,7,8,9,10,11,12,13,14,15,16,17-TETRADECAHYDRO-1H-CYCLOPENTA[A]PHENANTHREN-3-YL ACETATE 17-(2-BROMOACETYL)-3,17-DIHYDROXY-5,10,13-TRIMETHYLPERHYDROCYCLOPENTA[A]PHENANTHREN-11-ONE 5-ALPHA-ANDROSTAN-2-ALPHA-BROMO-17-BETA-OL-3-ONE ACETATE 5-ALPHA-PREGNAN-4-ALPHA-BROMO-17,21-DIOL-3,11,20-TRIONE 21-ACETATE 5BETA-PREGNAN-21-BROMO-3ALPHA,17ALPHA-DIOL-11,20-DIONE flavanol
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