product information
(1R,2s,5r)-2-Isopropyl-5-methylcyclohexanol  
CAS number: 98167-53-4
Groups: All Chemicals
Information:
IUPAC Name: (1R,2s,5r)-2-isopropyl-5-methylcyclohexanol  

CAS Number: 98167-53-4

Chemical Formula: C10H20O

Synonyms: 15785_RIEDEL, (1alpha,2beta,5alpha)-5-methyl-2(1-methylethyl)cyclohexanol, (1R-(1-alpha,2-beta,5-alpha))-5-Methyl-2-(1-methylethyl)cyclohexanol, (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexanol, (1R,2S,5R)-2-Isopropyl-5-methylcyclohexanol, (1R,2S,5R)-5-methyl-2-(1-methylethyl)cyclohexanol, (1R,2S,5R)-5-methyl-2-(propan-2-yl)cyclohexan-1-ol, (1R,2S,5R)-5-methyl-2-propan-2-yl-cyclohexan-1-ol, (1R,2S,5R)-5-methyl-2-propan-2-ylcyclohexan-1-ol, (1R,2S,5R)-(−)-Menthol, (1r,2s,5r)-(-)-menthol, (-)-(1R,3R,4S)-Menthol, (+-)-(1R*,3R*,4S*)-Menthol, (1R)-(-)-Menthol, 2216-51-5, 588733_ALDRICH, 5-Methyl-2-(1-methylethyl)cyclohexanol, 5-Methyl-2-(1-methylethyl)cyclohexanol, (1alpha,2beta,5alpha)-, 63660_FLUKA, (−)-Menthol, 89-78-1, 98167-53-4, AI3-52408, BB_NC-0057, BRN 1902288, BRN 3194263, BSPBio_003062, C00400, C10H20O, CCRIS 3728, CCRIS 375, CCRIS 4666, CHEBI:15409, Cyclohexanol, 2-isopropyl-5-methyl-, Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1.alpha.,2.beta.,5.alpha.)-, Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1alpha,2beta,5alpha)-, Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1R-(1alpha,2beta,5alpha))-, Cyclohexanol, 5-methyl-2-(1-methylethyl)-, [1R-(1.alpha.,2.beta.,5.alpha.)]-, Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1R-(1alpha,2beta,5alpha))- (9CI), Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1R,2S,5R)-, Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1R,2S,5R)-rel-, Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1R,3R,4S)-, D00064, DB00825, DivK1c_000820, d,l-Menthol, dl-Menthol, D-(-)-Menthol, EINECS 201-939-0, EINECS 218-690-9, EINECS 239-388-3, FEMA No. 2665, Headache crystals, Hexahydrothymol, HSDB 5662, HSDB 593, IDI1_000820, KBio1_000820, KBio2_000785, KBio2_003353, KBio2_005921, KBio3_002562, KBioSS_000785, Levomenthol, Levomenthol [BAN:INN], Levomenthol [INN:BAN], Levomentholum [INN-Latin], l-Menthol, l-(-)-Menthol, (L)-MENTHOL, L-Menthol crystals, l-Menthol (JP15), l-Menthol (natural), l-Menthol (TN), LMPR01020015, LS-2353, LS-89533, M2780_SIAL, Menthacamphor, (-)-menthol, (+-)-Menthol, MENTHOL, Menthol, (1alpha,2beta,5alpha)-Isomer, Menthol, (1R,3R,4S)-(-)-, Menthol, cis-1,3,trans-1,4-, Menthol, dl-, Menthol, l-, Menthol natural, Menthol natural, brazilian, Menthol racemic, Menthol racemique [French], Menthol (VAN), Menthomenthol, (-)-Menthyl alcohol, NCGC00164247-02, nchembio862-comp1, NCI-C50000, NINDS_000820, NSC2603, NSC 2603, NSC62788, NSC 62788, Peppermint camphor, p-Menthan-3-ol, Racementhol, Racementhol [INN:BAN], Racementholum [INN-Latin], Racementol [INN-Spanish], Racemic menthol, rac-Menthol, (R)-(-)-Menthol, SDCCGMLS-0066659.P001, SPBio_000869, Spectrum_000305, SPECTRUM1503134, Spectrum2_000855, Spectrum3_001561, Spectrum5_001060, Tra-kill tracheal mite killer, (-)-trans-p-Menthan-cis-ol, U.S.P. Menthol, W266523_ALDRICH, W266558_ALDRICH, W266590_ALDRICH, WLN: L6TJ AY1&1 BQ D1, WLN: L6TJ AY1&1 DQ D1 -L, ZINC01482164

Product Info: Sodium borohydride is a milder reducing agent, can be used in aqueous solution. It converts selectively aldehydes and ketones the corresponding alcohols in the manufacture of pharmaceuticals and other fine chemicals. It will not react with esters, amides, or carboxylic acids, the more powerful reducing agent lithium aluminum hydride(LAH) is used to reduce these compounds. LAH is the more powerful reducing agent than sodium borohydride due to the weaker Al-H bond compared to the B-H bond. The reactivity of sodium borohydride can be modified by addition of iodine or methanol in BH3-THF to reduce esters into the corresponding alcohols like the reaction of benzyl benzoate to benzyl alcohol. Sodium borohydride is used as a hydrogen source for fuel cell systems and a foaming agent for rubbers. Sodium cyanoborohydride converts certain alcohol groups to methylene groups. Sodium Cyanoborohydride is used as a selective amination reductant. It converts aldehydes (chemoselective), ketones (stereoselective) to the corresponding alcohols in the manufacture of pharmaceuticals and other fine chemicals. It is used in the reductive alkylation of amines, novel metals and oximes. Some examples of reducing agents are:

Diisobutylaluminum Hydride (DIBAL-H)
Dimethylsulfide Borane
Ferrous Ion
Formaldehyde
Formic Acid
Hydrazines
Hydrogen
Isopropanol
Lithium Aluminum Hydride
Low-valent Metal Compounds
Phenylsilane
Polymethylhydrosiloxane
Potassium Ferricyanide
Silanes
Sodium Bis(2-methoxyethoxy)Aluminumhydride
Sodium Hydrosulfite
Sodium Amalgam
Sodium And Potassium
Sodium Borohydride
Sodium Cyanoborohydride
Sodium Dithionite
Sodium Triacetoxyborohydride
Stannous Ion
Sulfite Compounds
Tin Hydrides
Triphenylphosphine
Zinc-mercury Amalgam
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