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4-tert-Butylbenzoic acid

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  • 4-tert-Butylbenzoic acid
  • 98-73-7
  • C11H14O2
  • 178.231
  • white to slightly yellow flakes
Inquiry

Factory Sells Best Quality 4-tert-Butylbenzoic acid 98-73-7 with ISO standards

  • Molecular Formula:C11H14O2
  • Molecular Weight:178.231
  • Appearance/Colour:white to slightly yellow flakes 
  • Vapor Pressure:0.0015mmHg at 25°C 
  • Melting Point:162-165 °C(lit.) 
  • Refractive Index:1.5201 (estimate) 
  • Boiling Point:283.3 °C at 760 mmHg 
  • PKA:4.38(at 25℃) 
  • Flash Point:134.9 °C 
  • PSA：37.30000 
  • Density:1.056 g/cm3 
  • LogP:2.68230 

4-tert-Butylbenzoic acid(Cas 98-73-7) Usage

Flammability and Explosibility

Nonflammable

Safety Profile

Moderately toxic by ingestion. Experimental reproductive effects. An irritant. Combustible when exposed to heat or flame. Incompatible with oxidzing materials. To fight fire, use foam, CO2, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes.

General Description

4-tert-Butylbenzoic acid was determined in water samples by means of liquid chromatography-electrospray ionisation mass spectrometry (LC-ESI-MS).

InChI:InChI=1/C11H14O2/c1-11(2,3)9-6-4-8(5-7-9)10(12)13/h4-7H,1-3H3,(H,12,13)/p-1

98-73-7 Relevant articles

Transformation of Thioacids into Carboxylic Acids via a Visible-Light-Promoted Atomic Substitution Process

Fu, Qiang,Liang, Fu-Shun,Lou, Da-Wei,Pan, Gao-Feng,Wang, Rui,Wu, Min,Xie, Kai-Jun

supporting information, p. 2020 - 2024 (2022/03/31)

A visible-light-promoted atomic substitu...

A Mild Heteroatom (O -, N -, and S -) Methylation Protocol Using Trimethyl Phosphate (TMP)-Ca(OH) 2Combination

Tang, Yu,Yu, Biao

, (2022/03/27)

A mild heteroatom methylation protocol u...

Cleavage of Carboxylic Esters by Aluminum and Iodine

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, p. 4254 - 4261 (2021/03/09)

A one-pot procedure for deprotecting car...

Kinetic study on the reaction of p-tert-butylbenzoic acid with methanol catalyzed by deep eutectic solvent based on choline chloride

Guo, Yuan,Tang, Linmao,Xue, Weilan,Zeng, Zuoxiang

, p. 1241 - 1252 (2021/08/12)

The synthesis of methyl p-tert-butylbenz...

98-73-7 Process route

2-[4-(1,1-dimethylethyl)phenyl]-6-methyl-4H-3,1-benzoxazin-4-one
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2-[4-(1,1-dimethylethyl)phenyl]-6-methyl-4H-3,1-benzoxazin-4-one

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26537-19-9

methyl 4-tert-butylbenzoate

4-(1,1-dimethylethyl)benzoic acid
98-73-7

4-(1,1-dimethylethyl)benzoic acid

methyl 2-[4-(1,1-dimethylethyl)benzamido]-5-methyl-benzoate
117145-67-2

methyl 2-[4-(1,1-dimethylethyl)benzamido]-5-methyl-benzoate

2-<4-(1,1-dimethylethyl)benzamido>-5-methyl-N-(2-carboxy-4-methylphenyl)benzamide
117145-79-6

2-<4-(1,1-dimethylethyl)benzamido>-5-methyl-N-(2-carboxy-4-methylphenyl)benzamide

Conditions
Conditions Yield
With hydrogenchloride; In methanol; for 20h; Further byproducts given; Heating;
44%
methanol
67-56-1

methanol

(E)-1,1'-(1,2-ethenediyl)bis(4-butyl)benzene
79135-54-9,114530-47-1,123356-27-4,64392-50-3

(E)-1,1'-(1,2-ethenediyl)bis(4-butyl)benzene

4-tert-Butylbenzaldehyde
939-97-9

4-tert-Butylbenzaldehyde

methyl 4-tert-butylbenzoate
26537-19-9

methyl 4-tert-butylbenzoate

4-(1,1-dimethylethyl)benzoic acid
98-73-7

4-(1,1-dimethylethyl)benzoic acid

Conditions
Conditions Yield
With iodine; oxygen; trifluoroacetic acid; In ethyl acetate; for 20h; Irradiation;
36 %Spectr.
32 %Spectr.
12 %Spectr.

98-73-7 Upstream products

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98-73-7 Downstream products

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    4-tert-butyl-benzoic acid-(2-dibutylamino-ethyl ester)

  • 14377-38-9
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    4-t-Butylbenzoesaeure-diethylaminoethylester

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