3,5-Di-tert-butyl-4-hydroxybenzoic acid
- CAS: 1421-49-4
- Purity: 99%
- Manufacturer Supply Best Quality 3,5-Di-tert-butyl-4-hydroxybenzoic acid 1421-49-4 with Efficient Transportation
Manufacturer Supply Best Quality 3,5-Di-tert-butyl-4-hydroxybenzoic acid 1421-49-4 with Efficient Transportation
- Molecular Formula: C15H22O3
- Molecular Weight: 250.338
- Appearance/Colour: Light yellow to beige crystalline powder
- Vapor Pressure: 3.28E-05mmHg at 25°C
- Melting Point: 206-209 °C
- Refractive Index: 1.5600 (estimate)
- Boiling Point: 340.6 °C at 760 mmHg
- PKA: 4.77±0.10(Predicted)
- Flash Point: 174 °C
- PSA： 57.53000
- Density: 1.07 g/cm3
- LogP: 3.68540
3,5-Di-tert-butyl-4-hydroxybenzoic acid(Cas 1421-49-4) Usage
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General Description |
3,5-Di-tert-butyl-4-hydroxybenzoic acid is a metabolite of butylated hydroxytoluene. |
InChI:InChI=1/C15H22O3/c1-14(2,3)10-7-9(13(17)18)8-11(12(10)16)15(4,5)6/h7-8,16H,1-6H3,(H,17,18)/p-1
1421-49-4 Relevant articles
3. 5 - Di-tert-butyl -4 - hydroxy benzoic acid production method (by machine translation)
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Paragraph 0048-0072, (2019/01/16)
The invention discloses a 3, 5 - di-tert...
Synthetic method for antitumor drug intermediate 3,5-di-tert-butyl-4-hydroxybenzoic acid
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Paragraph 0015; 0020; 0024; 0025-0029, (2018/07/30)
The invention discloses a synthetic meth...
Preparation method of propofol and structural analogues of propofol
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Paragraph 0096, (2017/08/28)
The invention relates to a preparation m...
Bismuth-based cyclic synthesis of 3,5-di-tert-butyl-4-hydroxybenzoic acid via the oxyarylcarboxy dianion, (O2CC6H2 tBu2O)2-
Kindra, Douglas R.,Evans, William J.
, p. 3052 - 3054 (2014/03/21)
3,5-Di-tert-butyl-4-hydroxybenzoic acid ...
1421-49-4 Process route
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1918-11-2
terbucarb
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128-37-0
2,6-di-tert-butyl-4-methyl-phenol
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88-26-6
3,5-di-tert-butyl-4-hydroxybenzyl alcohol
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1421-49-4
3,5-Di-tert-butyl-4-hydroxybenzoic acid
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carbamate de 2,6-ditertiobutyl 4-methylphenyle
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2,6-di-tert-butyl-4-carboxyphenyl carbamate
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1620-98-0
3,5-di-t-butyl-4-hydroxybenzaldehyde
| Conditions | Yield |
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identification of degradation products in environmental water from Golf Courses;
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69901-41-3
1-isopropyl-3,5-di-tert-butyl-4-oxo-2,5-cyclohexadienyl 3,5-di-tert-butyl-4-hydroxyperbenzoate
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719-22-2
2,6-Di-tert-butyl-1,4-benzoquinone
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5427-03-2
2,6-di-tert-butyl-4-isopropylphenol
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128-38-1
4,4'-dihydroxy-3,3',5,5'-tetra-tert-butylbiphenyl
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1421-49-4
3,5-Di-tert-butyl-4-hydroxybenzoic acid
| Conditions | Yield |
|---|---|
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With
potassium tert-butylate;
In
N,N-dimethyl-formamide; Petroleum ether; benzene;
at -78 - -60 ℃;
for 1h;
Further byproducts given;
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52 % Spectr.
80 % Spectr. 16 % Spectr. 9 % Spectr. |
1421-49-4 Upstream products
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1620-98-0
3,5-di-t-butyl-4-hydroxybenzaldehyde
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69901-39-9
1-methyl-3,5-di-tert-butyl-4-oxo-2,5-cyclohexadienyl 3,5-di-tert-butyl-4-hydroxyperbenzoate
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69901-40-2
1-ethyl-3,5-di-tert-butyl-4-oxo-2,5-cyclohexadienyl 3,5-di-tert-butyl-4-hydroxyperbenzoate
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69901-41-3
1-isopropyl-3,5-di-tert-butyl-4-oxo-2,5-cyclohexadienyl 3,5-di-tert-butyl-4-hydroxyperbenzoate
1421-49-4 Downstream products
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88-26-6
3,5-di-tert-butyl-4-hydroxybenzyl alcohol
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64506-75-8
β-{4-[2-(3,5-di-tert.-butyl-4-hydroxybenzamido)-ethyl]-phenyl}-propionic acid
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78649-07-7
C24 H38 NO4
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137937-56-5
2-ethylhexyl 3,5-di-tert-butyl-4-hydroxybenzoate
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