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[ CAS No. 37942-07-7 ] {[proInfo.proName]}

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Chemical Structure| 37942-07-7
Chemical Structure| 37942-07-7
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Product Details of [ 37942-07-7 ]

CAS No. :37942-07-7 MDL No. :MFCD00191998
Formula : C15H22O2 Boiling Point : No data available
Linear Structure Formula :OCHC6H2OH(C(CH3)3)2 InChI Key :RRIQVLZDOZPJTH-UHFFFAOYSA-N
M.W : 234.33 Pubchem ID :688023
Synonyms :

Safety of [ 37942-07-7 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 37942-07-7 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 37942-07-7 ]

[ 37942-07-7 ] Synthesis Path-Downstream   1~16

  • 1
  • [ 37942-07-7 ]
  • (R,R)-1,2-diaminocyclohexane tartrate [ No CAS ]
  • [ 135616-40-9 ]
  • 2
  • [ 37942-07-7 ]
  • (1R,2R)-1,2-diaminocyclohexane tartrate [ No CAS ]
  • [ 135616-40-9 ]
YieldReaction ConditionsOperation in experiment
70% (R,R)-N,N'-Bis(5-3-tert-butyl-salicylidene)-l,2-cyclohexanediamine was synthesized following a similar procedure described by Jacobsen E. N., Zhang W., Muci A. R., Ecker J. R., and Deng L. Highly Enantioselective Epoxidation Catalysts Derived from 1,2- Diaminocyclohexane, J. Am. Chem. Soc, 113, 7063-7064 (1991). To a 250 mL round bottom flask was added 2.0053 g (8.5573 mmol) of 3,5 -tert butyl-2-hydroxybenzaldehyde that was dissolved in 20 mL absolute ethanol. Concurrently, (R5R)- 1,2-diammoniumcyclohexane mono-(+)-tartrate salt {see Larrow J. F., Jacobsen E. N., Gao Y., Hong Y., Nie X., and Zepp C. M., A Practical Process for the Large-Scale Preparation of (R,R)-N,N'-Bis(3,5-Di-tert- butylsalicylidene)-l,2-Cyclohexanediaminomanganese (III) Chloride, a Highly Enantioselective Epoxidation Catalyst, J. Org. Chem., 59, 1939-1940 (1994); (1.1219 g, 4.2451 mmol) was dissolved in a basic (NaOH) 0.2 M aqueous/absolute ethanol solution (1 :2). This salt solution was added dropwise to the benzaldehyde solution and the mixture was refluxed under nitrogen for 1 hour. The reaction mixture was filtered using a 60 mL medium frit and washed with 95% ethanol. The product was then extracted into methylene chloride. The frit was washed with additional methylene chloride until the solid was colorless. The solvent was removed under reduced pressure to yield 1.6843 gm (70%) of a yellow solid. 1H NMR: (CDCl3, ppm) delta = 1.24 (s, 9H); 1.41 (s, 9H); 1.45 (m, IH); 1.65 - 1.8 (m, IH); 1.8 - 2.0 (m, 2H); 3.32 (m, IH); 6.98 (d, IH); 7.30 (d, IH); 8.30 (s, IH); 13.72 (s, IH).
  • 3
  • [ 37942-07-7 ]
  • [ 4506-66-5 ]
  • N,N',N'',N'''-tetra-(3,5-di-tert-butylsalicylidene)-1,2,4,5-phenylenetetraamine [ No CAS ]
  • 4
  • [ 37942-07-7 ]
  • [ 191480-63-4 ]
  • [ 135616-40-9 ]
  • 5
  • [ 37942-07-7 ]
  • [ 4506-66-5 ]
  • (2,4-di-tert-butyl-6-({2,4,5-tri-[(3,5-di-tert-butyl-2-hydroxy-benzylidene)-amino]-phenylimino}-methyl)-phenol) [ No CAS ]
  • 6
  • [ 37942-07-7 ]
  • (R,R)-1,2-diaminocyclohexane*(+)-tartric acid [ No CAS ]
  • [ 135616-40-9 ]
  • 7
  • [ 37942-07-7 ]
  • [ 21436-03-3 ]
  • [ 135616-40-9 ]
  • 8
  • [ 37942-07-7 ]
  • [ 24629-25-2 ]
  • 2,4-bis(1,1-dimethylethyl)-6-([(1S,2S)-1-hydroxymethyl-2-methylbutyl]imino}methyl)phenol [ No CAS ]
  • 9
  • [ 37942-07-7 ]
  • [ 24629-25-2 ]
  • [ 1159839-76-5 ]
  • 10
  • [ 37942-07-7 ]
  • [ 7474-78-4 ]
  • [ 1217433-15-2 ]
  • 11
  • [ 50-00-0 ]
  • [ 2934-05-6 ]
  • [ 37942-07-7 ]
  • 12
  • [ 37942-07-7 ]
  • [ 5978-75-6 ]
  • [ 1223561-32-7 ]
  • 13
  • [ 42726-73-8 ]
  • [ 37942-07-7 ]
  • tert-butyl 6,8-di-tert-butyl-2-oxo-2H-chromene-3-carboxylate [ No CAS ]
  • 14
  • [ 37942-07-7 ]
  • [ 68176-57-8 ]
  • C40H56N2O2 [ No CAS ]
  • 15
  • [ 37942-07-7 ]
  • [ 68176-57-8 ]
  • C40H54N2O2Pt [ No CAS ]
  • 16
  • [ 37942-07-7 ]
  • [ 4506-66-5 ]
  • 2,4-di-tert-butyl-6-((2,4,5-tri-[(3,5-di-tert-butyl-2-hydroxy-benzylidene)-amino]-phylimino)-methyl)-phenol [ No CAS ]
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Technical Information

? Acidity of Phenols ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Benzylic Oxidation ? Birch Reduction ? Blanc Chloromethylation ? Bucherer-Bergs Reaction ? Chan-Lam Coupling Reaction ? Clemmensen Reduction ? Complex Metal Hydride Reductions ? Corey-Chaykovsky Reaction ? Corey-Fuchs Reaction ? Electrophilic Substitution of the Phenol Aromatic Ring ? Etherification Reaction of Phenolic Hydroxyl Group ? Fischer Indole Synthesis ? Friedel-Crafts Reaction ? Grignard Reaction ? Halogenation of Phenols ? Hantzsch Dihydropyridine Synthesis ? Henry Nitroaldol Reaction ? Horner-Wadsworth-Emmons Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Julia-Kocienski Olefination ? Knoevenagel Condensation ? Leuckart-Wallach Reaction ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Mukaiyama Aldol Reaction ? Nozaki-Hiyama-Kishi Reaction ? Oxidation of Phenols ? Passerini Reaction ? Paternò-Büchi Reaction ? Pechmann Coumarin Synthesis ? Petasis Reaction ? Pictet-Spengler Tetrahydroisoquinoline Synthesis ? Preparation of Aldehydes and Ketones ? Preparation of Alkylbenzene ? Preparation of Amines ? Prins Reaction ? Reactions of Aldehydes and Ketones ? Reactions of Amines ? Reactions of Benzene and Substituted Benzenes ? Reformatsky Reaction ? Reimer-Tiemann Reaction ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Stetter Reaction ? Stobbe Condensation ? Tebbe Olefination ? Ugi Reaction ? Vilsmeier-Haack Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
Historical Records

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[ 37942-07-7 ]

Armodafinil Intermediates

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2-(Benzhydrylsulfinyl)acetic acid

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[ 37942-07-7 ]

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