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[ CAS No. 1620-98-0 ] {[proInfo.proName]}

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Chemical Structure| 1620-98-0
Chemical Structure| 1620-98-0
Structure of 1620-98-0 * Storage: {[proInfo.prStorage]}

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Product Details of [ 1620-98-0 ]

CAS No. :1620-98-0 MDL No. :MFCD00008826
Formula : C15H22O2 Boiling Point : -
Linear Structure Formula :((CH3)3C)2C6H2(OH)CHO InChI Key :DOZRDZLFLOODMB-UHFFFAOYSA-N
M.W : 234.33 Pubchem ID :73219
Synonyms :

Safety of [ 1620-98-0 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P305+P351+P338 UN#:N/A
Hazard Statements:H302-H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 1620-98-0 ]

* 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 [ 1620-98-0 ]

[ 1620-98-0 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 83465-22-9 ]
  • [ 1620-98-0 ]
  • [ 83470-52-4 ]
  • 2
  • [ 7504-94-1 ]
  • [ 1620-98-0 ]
  • 2,6-di-tert-butyl-4-(pyrimidin-2-ylhydrazonomethyl)phenol [ No CAS ]
  • 3
  • [ 120069-21-8 ]
  • [ 1620-98-0 ]
  • (E)-3-(3,5-Di-Tert-Butyl-4-Hydroxy-Phenyl)-2-(Propane-2-Sulfonyl)-Acrylonitrile [ No CAS ]
YieldReaction ConditionsOperation in experiment
34% Step A: The title compound was prepared from 3,5-di-tert-butyl-4-hydroxybenzaldehyde and propane-2-sulphonylacetonitrile in 34% yield 1H NMR (DMSO-d6): delta ppm 1.32 (d, J=6.78 Hz, 6 H) 1.41 (s, 18 H) 3.56 (m, 1 H) 7.98 (s, 2 H) 8.16 (s, 1 H) 8.41 (s, 1 H); HPLC-MS (Method A): m/z=464 (M+1); Rt=5.0 min.
  • 4
  • [ 57497-39-9 ]
  • [ 1620-98-0 ]
  • [ 29211-05-0 ]
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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

Pharmaceutical Intermediates of
[ 1620-98-0 ]

Darbufelone Intermediates

Chemical Structure| 556-90-1

[ 556-90-1 ]

2-aminothiazol-4(5H)-one

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[ 1620-98-0 ]

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