1-Adamantanemethanol

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 Structure
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
pka15.51±0.10(Predicted)
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)
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
AKOS BB-8907 FMOC-DAB(ADPOC)-OH 1-(1-ADAMANTYL)PROPAN-1-OL methylol cellulose FMOC-DAP(ADPOC)-OH 3,5-DIMETHYL-1-ADAMANTANEMETHANOL 2-Adamantone-5-carboxylic acid AKOS BC-1052 9-fluoro-11beta,17-dihydroxy-16beta-methylpregna-1,4-diene-3,20-dione 21-[tricyclo[3.3.1.13,7]dec-1-ylformate] Hydroxymethyl cyclomaltoheptaose-1-adamantanemethanol 1-(1-ADAMANTYL)ETHANOL FMOC-LYS(ADPOC)-OH AKOS BC-0746 ISOPROPYL ADAMANTAN-1-CARBOXYLATE CARBOXYMETHYLCELLULOSE SODIUM SALT ADAMANTANE-1-CARBOXYLIC ACID METHYL ESTER AKOS BB-8996

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