ChemicalBook--->CAS DataBase List--->23504-03-2

23504-03-2

23504-03-2 Structure

23504-03-2 Structure
IdentificationBack Directory
[Name]

4-isopropylresorcinol
[CAS]

23504-03-2
[Synonyms]

Einecs 245-703-5
4-isopropylresorcinol
4-Isopropylbenzene-1,3-diol
4-propan-2-ylbenzene-1,3-diol
4-(1-Methylethyl)-1,3-benzenediol
1,3-Benzenediol, 4-(1-Methylethyl)-
4-Isopropylresorcinol, 1,3-Dihydroxy-4-(prop-2-yl)benzene
[EINECS(EC#)]

245-703-5
[Molecular Formula]

C9H12O2
[MDL Number]

MFCD05663778
[MOL File]

23504-03-2.mol
[Molecular Weight]

152.19
Questions And AnswerBack Directory
[Uses]

4-Isopropylbenzene-1,3-diol acts as a reagent in the synthesis of 3,5-disubstituted-4-alkynylisoxozales as HSP90 inhibitors against various human cancer cell lines.
Chemical PropertiesBack Directory
[Melting point ]

105 °C
[Boiling point ]

114 °C(Press: 0.2 Torr)
[density ]

1.116±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

DMSO (Sparingly), Methanol (Slightly)
[form ]

solid
[pka]

10.03±0.18(Predicted)
[color ]

Off-white
[InChI]

InChI=1S/C9H12O2/c1-6(2)8-4-3-7(10)5-9(8)11/h3-6,10-11H,1-2H3
[InChIKey]

LNFVQIGQENWZQN-UHFFFAOYSA-N
[SMILES]

C1(O)=CC=C(C(C)C)C(O)=C1
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
[Signal word ]

Danger
[Hazard statements ]

H302-H314-H317-H412
[Precautionary statements ]

P260-P280-P309+P311
[HazardClass ]

IRRITANT
[HS Code ]

2907290090
Spectrum DetailBack Directory
[Spectrum Detail]

4-isopropylresorcinol(23504-03-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

Benzene, 1-(1-Methylethenyl)-2,4-bis(phenylMethoxy)-

747414-16-0

4-isopropylresorcinol

23504-03-2

The general procedure for the synthesis of 4-isopropylresorcinol from (((4-(1-propen-2-yl)-1,3-phenylene)bis(oxy))bis(methylene))bis(benzene))diphenyl was as follows: a mixture of compound 17 (3 g, 9.08 mmol) with 10% Pd/C (30 wt%) in ethanol (48 mL) was placed in a hydrogen atmosphere and stirred for 18 hours at room temperature. Upon completion of the reaction, the solid catalyst was removed by filtration through a diatomaceous earth pad and the filter cake was washed with methanol. The filtrate was concentrated under reduced pressure and the resulting crude product was purified by silica gel fast column chromatography (eluent ratio: ethyl acetate:hexane=1:1) to afford compound 18 as a white crystalline solid (1.35 g, 98% yield). The physical and spectral data of the compound were consistent with those reported in the literature: melting point 87~89 °C. 1H NMR (400 MHz, DMSO-d6) δ 9.02 (s, 1H), 8.90 (s, 1H), 6.85 (d, J=8.2 Hz, 1H), 6.26 (d, J=2.7 Hz, 1H), 6.16 (dd, J=8.2,2.3 Hz , 1H), 3.16-2.98 (m, 1H), 1.18-1.04 (s, 6H); 13C NMR (100 MHz, DMSO-d6) δ 155.59,154.78,125.87,124.56,105.67,102.11,25.52,22.64. ESI-MS: m/z = 170 (M +H2O)+.

[References]

[1] Bioorganic and Medicinal Chemistry Letters, 2018, vol. 28, # 23-24, p. 3658 - 3664
[2] Patent: US2009/76006, 2009, A1. Location in patent: Page/Page column 32; 41
[3] Bioorganic and Medicinal Chemistry Letters, 2015, vol. 25, # 16, p. 3129 - 3134
[4] European Journal of Medicinal Chemistry, 2014, vol. 87, p. 765 - 781
[5] Patent: CN103724269, 2016, B. Location in patent: Paragraph 0388; 0389; 0399; 0400; 0401; 0402
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