1-Adamantanemethanol

1-Adamantanemethanol
  • CAS No.:770-71-8
Other grades of this product :
1-Adamantanemethanol Basic information
Product Name:1-Adamantanemethanol
Synonyms:AKOS BC-0668;RARECHEM AQ TC 1004;SALOR-INT L496014-1EA;LABOTEST-BB LT00007819;CHEMBRDG-BB 4013930;1-adamantanemethannol;1-Adamantlcarbinol;Adamantanemethanol
CAS:770-71-8
MF:C11H18O
MW:166.26
EINECS:212-225-3
Product Categories:Adamantane derivatives;Alkohols;Adamantanes
Mol File:770-71-8.mol
1-Adamantanemethanol Chemical Properties
Melting point 114-117 °C (lit.)
Boiling point 234.5°C (rough estimate)
density 0.8802 (rough estimate)
refractive index 1.5000 (estimate)
storage temp. Sealed in dry,Room Temperature
form Crystalline Powder
color White
Water Solubility Insoluble in water. Solubility in methanol (almost transparency).
BRN 1853339
InChIKeyMDVGOOIANLZFCP-UHFFFAOYSA-N
CAS DataBase Reference770-71-8(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 22-24/25-36-26
WGK Germany 3
HazardClass IRRITANT
HS Code 29061900
MSDS Information
ProviderLanguage
1-Adamantanemethanol English
SigmaAldrich English
ACROS English
ALFA English
1-Adamantanemethanol Usage And Synthesis
Description1-Adamantanemethanol acts as guest molecule and forms β-cyclodextrin complexes. It reacts with 3,4,5,6-tetrafluorophthalonitrile to yield 3,4,5,6-tetra-(1-adamantylmethoxy)phthalonitrile.
Chemical Propertieswhite crystalline powder
Uses1-Adamantanemethanol was used in the synthesis of axially disubstituted silicon(IV) phthalocyanines. It is used as a reagent in the synthesis of adamantane and noradamantane based histone deacetylase (HDAC) inhibitors for the treatment of cancer. It is also used as a reagent in the synthesis of (1-adamantyl)methyl glycidyl ether, a versatile building block for living polymerization. References Gopalan, B., et al.: Bioorg. Med. Chem. Lett., 23, 2532 (2013); Suzuki, T., et al.: J. Med. Chem., 55, 9562 (2012); Moers, C., et al.: Macromol. Rapid Comm., 35, 1075 (2014)
Uses1-Adamantanemethanol was used in the synthesis of axially disubstituted silicon(IV) phthalocyanines.
Purification MethodsDissolve the adamantane in Et2O, wash it with aqueous 0.1N NaOH and H2O, dry over CaCl2, evaporate and recrystallise the residue from aqueous MeOH. [Stetter et al. Chem Ber 92 1629 1959, Beilstein 6 IV 400.]
1-Adamantanemethanol Preparation Products And Raw materials
Preparation Products2-(1-Adamantyl)oxirane-->1-Adamantanecarbonitrile-->ADAMANTAN-1-YLMETHYL ACETATE-->ADAMANTANE-1-CARBOXYLIC ACID METHYL ESTER

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