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27914-73-4

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27914-73-4 Usage

General Description

4-Acetoxy-benzoylchloride, also known as Benzoyl chloride, 4'-(acetyloxy), is a chemical compound with the formula C10H7ClO3. It is used in the production of various polymers, pharmaceuticals, and dyes. Due to its reactive nature, it is often used as an acylating agent in chemical synthesis. It appears as a light yellow to brown liquid, has a strong odor, and it's sensitive to moisture. Handling of 4-Acetoxy-benzoylchloride should be done with caution as it may cause burns to the skin, eyes, and mucous membranes. It is also combustible and poses a danger to the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 27914-73-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,9,1 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 27914-73:
(7*2)+(6*7)+(5*9)+(4*1)+(3*4)+(2*7)+(1*3)=134
134 % 10 = 4
So 27914-73-4 is a valid CAS Registry Number.

27914-73-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Aldrich

  • (740470)  4-(Acetoxy)benzoyl chloride  97%

  • 27914-73-4

  • 740470-1G

  • 414.18CNY

  • Detail

27914-73-4Synthetic route

4-acetyloxy-benzoic acid
2345-34-8

4-acetyloxy-benzoic acid

4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

Conditions
ConditionsYield
With oxalyl dichloride at 20℃; for 4h;100%
With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 20℃; for 4h;100%
With thionyl chloride at 79℃; for 4h; Heating / reflux;99%
C11H25NO2Si
748122-53-4

C11H25NO2Si

3-(chlorocarbonyl)phenyl acetate
16446-73-4

3-(chlorocarbonyl)phenyl acetate

4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

Conditions
ConditionsYield
In dichloromethane 1.) 0 deg C, 30 min, 2.) RT, 1 h;
4-hydroxy-benzoic acid
99-96-7

4-hydroxy-benzoic acid

4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 63 percent / aq. NaOH / 1 h / cooling
2: thionyl chloride; N,N-dimethylformamide / 5 h / 70 °C
View Scheme
With thionyl chloride; sulfuric acid In acetic anhydride
Multi-step reaction with 2 steps
1: 6 h / Reflux
2: thionyl chloride / 2 h / Reflux
View Scheme
oxalyl dichloride
79-37-8

oxalyl dichloride

4-acetyloxy-benzoic acid
2345-34-8

4-acetyloxy-benzoic acid

4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

4-acetyloxy-benzoic acid
2345-34-8

4-acetyloxy-benzoic acid

N-cyclohexyl-cyclohexanamine
101-83-7

N-cyclohexyl-cyclohexanamine

4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

Conditions
ConditionsYield
With thionyl chloride In dichloromethane
methyl 4-acetoxybenzoate
24262-66-6

methyl 4-acetoxybenzoate

4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

Conditions
ConditionsYield
With thionyl chloride In chloroform; N,N-dimethyl-formamide Reflux;
tert-butyl 4-hydroxybenzoate
25804-49-3

tert-butyl 4-hydroxybenzoate

4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: pyridine / tetrahydrofuran / 16.25 h / 0 - 20 °C / Inert atmosphere
2: thionyl chloride; water / 16 h / 23 °C / Sealed tube
View Scheme
tert-butyl 4-acetoxybenzoate
59854-09-0

tert-butyl 4-acetoxybenzoate

4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

Conditions
ConditionsYield
With thionyl chloride; water at 23℃; for 16h; Sealed tube;
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

1'-[(3S)-3-(3,4-dichlorophenyl)-4-(methylamino)butyl]-N,N-dimethyl-1,4'-bipiperidine-4'-carboxamide trihydrochloride

1'-[(3S)-3-(3,4-dichlorophenyl)-4-(methylamino)butyl]-N,N-dimethyl-1,4'-bipiperidine-4'-carboxamide trihydrochloride

4-({[(2S)-2-(3,4-dichlorophenyl)-4-{4'-[(-N,N-dimethylamino)-carbonyl]1,4'-bipiperidin-1'-yl}butyl](methyl)amino}carbonyl)phenyl acetate

4-({[(2S)-2-(3,4-dichlorophenyl)-4-{4'-[(-N,N-dimethylamino)-carbonyl]1,4'-bipiperidin-1'-yl}butyl](methyl)amino}carbonyl)phenyl acetate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃; for 15h;100%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

R-(-)-4-ethylhexan-2-ol
220150-55-0

R-(-)-4-ethylhexan-2-ol

(R)-4-acetoxy-1-(3-ethyl-1-methylpentyloxycarbonyl)benzene
443682-67-5

(R)-4-acetoxy-1-(3-ethyl-1-methylpentyloxycarbonyl)benzene

Conditions
ConditionsYield
With pyridine In dichloromethane; water100%
With pyridine In toluene at 20℃; for 15h;97%
With pyridine In water; toluene92%
With pyridine In water; toluene63 g (0.215 mol. yield 97%)
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

(R)-1-methyloctyl-4-acetoxyphenylcarboxylate
479629-72-6

(R)-1-methyloctyl-4-acetoxyphenylcarboxylate

Conditions
ConditionsYield
With pyridine In dichloromethane; water100%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

1'-[(3S)-3-(3,4-dichlorophenyl)-4-(methylamino)butyl]-N,N-dimethyl-1,4'-bipiperidine-4'-carboxamide hydrochloride

1'-[(3S)-3-(3,4-dichlorophenyl)-4-(methylamino)butyl]-N,N-dimethyl-1,4'-bipiperidine-4'-carboxamide hydrochloride

4-({[(2S)-2-(3,4-dichlorophenyl)-4-{4'-[(-N,N-dimethylamino)-carbonyl]1,4'-bipiperidin-1'-yl}butyl](methyl)amino}carbonyl)phenyl acetate

4-({[(2S)-2-(3,4-dichlorophenyl)-4-{4'-[(-N,N-dimethylamino)-carbonyl]1,4'-bipiperidin-1'-yl}butyl](methyl)amino}carbonyl)phenyl acetate

Conditions
ConditionsYield
Stage #1: 4-acetoxybenzoyl chloride; 1'-[(3S)-3-(3,4-dichlorophenyl)-4-(methylamino)butyl]-N,N-dimethyl-1,4'-bipiperidine-4'-carboxamide hydrochloride With triethylamine In dichloromethane at 20℃; for 15h;
Stage #2: With potassium hydroxide In tert-butyl methyl ether; water; ethyl acetate
100%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

N,N-diethyl-2-(piperazin-1-yl)acetamide
40004-14-6

N,N-diethyl-2-(piperazin-1-yl)acetamide

Acetic acid 4-(4-diethylcarbamoylmethyl-piperazine-1-carbonyl)-phenyl ester; hydrochloride

Acetic acid 4-(4-diethylcarbamoylmethyl-piperazine-1-carbonyl)-phenyl ester; hydrochloride

Conditions
ConditionsYield
In diethyl ether at -15 - -10℃; for 0.166667h;98%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

methyl 2-amino-6-phenyl-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate
119004-72-7

methyl 2-amino-6-phenyl-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate

methyl 2-(4-hydroxybenzamido)-6-phenyl-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate

methyl 2-(4-hydroxybenzamido)-6-phenyl-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate

Conditions
ConditionsYield
Stage #1: 4-acetoxybenzoyl chloride; methyl 2-amino-6-phenyl-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃;
Stage #2: With lithium hydroxide monohydrate In tetrahydrofuran; methanol at 40℃; for 0.5h;
98%
1-(1-methylethyl)piperazine
4318-42-7

1-(1-methylethyl)piperazine

4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

Acetic acid 4-(4-isopropyl-piperazine-1-carbonyl)-phenyl ester; hydrochloride

Acetic acid 4-(4-isopropyl-piperazine-1-carbonyl)-phenyl ester; hydrochloride

Conditions
ConditionsYield
In diethyl ether at -15 - -10℃; for 0.166667h;97%
1-(2-(diethylamino)ethyl)piperazine
4038-92-0

1-(2-(diethylamino)ethyl)piperazine

4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

Acetic acid 4-[4-(2-diethylamino-ethyl)-piperazine-1-carbonyl]-phenyl ester; hydrochloride

Acetic acid 4-[4-(2-diethylamino-ethyl)-piperazine-1-carbonyl]-phenyl ester; hydrochloride

Conditions
ConditionsYield
In diethyl ether at -15 - -10℃; for 0.166667h;97%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

1-n-propylpiperazine
21867-64-1

1-n-propylpiperazine

Acetic acid 4-(4-propyl-piperazine-1-carbonyl)-phenyl ester; hydrochloride

Acetic acid 4-(4-propyl-piperazine-1-carbonyl)-phenyl ester; hydrochloride

Conditions
ConditionsYield
In diethyl ether at -15 - -10℃; for 0.166667h;97%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

4-fluoropyridin-2-amine
944401-77-8

4-fluoropyridin-2-amine

4-[(4-fluoropyridin-2-yl)carbamoyl]phenyl acetate

4-[(4-fluoropyridin-2-yl)carbamoyl]phenyl acetate

Conditions
ConditionsYield
In pyridine; dichloromethane at 20℃;97%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

butyl-iodo-manganese
62485-87-4

butyl-iodo-manganese

Acetic acid 4-pentanoyl-phenyl ester
97037-82-6

Acetic acid 4-pentanoyl-phenyl ester

Conditions
ConditionsYield
In diethyl ether for 2h; Ambient temperature;96%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

1-phenylmethylpiperazine
2759-28-6

1-phenylmethylpiperazine

Acetic acid 4-(4-benzyl-piperazine-1-carbonyl)-phenyl ester; hydrochloride

Acetic acid 4-(4-benzyl-piperazine-1-carbonyl)-phenyl ester; hydrochloride

Conditions
ConditionsYield
In diethyl ether at -15 - -10℃; for 0.166667h;96%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

benzene
71-43-2

benzene

4-acetoxybenzophenone
13031-44-2

4-acetoxybenzophenone

Conditions
ConditionsYield
With aluminium trichloride Friedels-Crafts benzoylation; Heating;95%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

N-trimethylsilylmethylamine
18166-02-4

N-trimethylsilylmethylamine

4-{[(trimethylsilyl)methyl]carbamoyl}phenyl acetate

4-{[(trimethylsilyl)methyl]carbamoyl}phenyl acetate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃; Inert atmosphere;94%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

2-amino-6-(1,1-dimethylethyl)-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxylic acid methyl ester
213192-26-8

2-amino-6-(1,1-dimethylethyl)-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxylic acid methyl ester

methyl 2-(4-acetoxybenzamido)-6-(tert-butyl)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate

methyl 2-(4-acetoxybenzamido)-6-(tert-butyl)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃;93%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

R-(-)-4-ethylhexan-2-ol
220150-55-0

R-(-)-4-ethylhexan-2-ol

(R)-3-ethyl-1-methylpentyl-4-acetoxybenzoate

(R)-3-ethyl-1-methylpentyl-4-acetoxybenzoate

Conditions
ConditionsYield
With pyridine In toluene at 20℃; for 3h;92%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

isopropylamine
75-31-0

isopropylamine

4-(isopropylcarbamoyl)phenyl acetate

4-(isopropylcarbamoyl)phenyl acetate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0 - 20℃; for 6h; Inert atmosphere; Schlenk technique;92%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

N-(3,5-dimethoxyphenyl)-N-methylamine
118684-17-6

N-(3,5-dimethoxyphenyl)-N-methylamine

4-{[(3,5-dimethoxyphenyl)(methyl)amino]carbonyl}phenyl acetate
1132660-78-6

4-{[(3,5-dimethoxyphenyl)(methyl)amino]carbonyl}phenyl acetate

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 0℃; for 1h;91%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

3-(5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl)benzohydrazide
1169389-62-1

3-(5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl)benzohydrazide

4-(2-(3-(5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl)benzoyl)hydrazinecarbonyl)phenyl acetate
1169389-79-0

4-(2-(3-(5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl)benzoyl)hydrazinecarbonyl)phenyl acetate

Conditions
ConditionsYield
Stage #1: 4-acetoxybenzoyl chloride; 3-(5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl)benzohydrazide In tetrahydrofuran; N,N-dimethyl-formamide at 20℃; for 18h;
Stage #2: With pyridine In tetrahydrofuran; N,N-dimethyl-formamide for 1h;
90.9%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

hydroquinone
123-31-9

hydroquinone

1,4-bis(4-acetoxybenzoyloxy)-benzene
79066-38-9

1,4-bis(4-acetoxybenzoyloxy)-benzene

Conditions
ConditionsYield
With pyridine In 1,2-dichloro-ethane at 20℃; for 48h; Inert atmosphere;90%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

O-benzylhydoxylamine hydrochloride
2687-43-6

O-benzylhydoxylamine hydrochloride

4-((benzyloxy)carbamoyl)phenyl acetate

4-((benzyloxy)carbamoyl)phenyl acetate

Conditions
ConditionsYield
With sodium hydrogencarbonate In tetrahydrofuran at 20℃; for 1h;90%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

4-(5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl)benzoylhydrazine
1169389-56-3

4-(5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl)benzoylhydrazine

4-(2-(4-(5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl)benzoyl)hydrazinecarbonyl)phenyl acetate
1169389-75-6

4-(2-(4-(5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl)benzoyl)hydrazinecarbonyl)phenyl acetate

Conditions
ConditionsYield
Stage #1: 4-acetoxybenzoyl chloride; 4-(5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl)benzoylhydrazine In tetrahydrofuran; N,N-dimethyl-formamide at 20℃; for 19h;
Stage #2: With pyridine In tetrahydrofuran; N,N-dimethyl-formamide for 1.5h;
90%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

o-(methylamino)acetophenone
1859-75-2

o-(methylamino)acetophenone

4-{[(2-acetylphenyl)(methyl)amino]carbonyl}phenyl acetate
1319210-04-2

4-{[(2-acetylphenyl)(methyl)amino]carbonyl}phenyl acetate

Conditions
ConditionsYield
With triethylamine In tetrahydrofuran at 70℃; for 3h;90%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

chloro-p-hydroquinone
615-67-8

chloro-p-hydroquinone

C24H17ClO8

C24H17ClO8

Conditions
ConditionsYield
With pyridine In 1,2-dichloro-ethane at 20℃; for 48h; Inert atmosphere;90%
With pyridine In 1,2-dichloro-ethane
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

C17H20O8

C17H20O8

Conditions
ConditionsYield
With pyridine at 20℃; for 0.5h;90%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

1,1-bis-(4-hydroxyphenyl)-3,3,5-trimethyl cyclohexane
129188-99-4

1,1-bis-(4-hydroxyphenyl)-3,3,5-trimethyl cyclohexane

(3,3,5-trimethylcyclohexane-1,1-diyl)bis(1,4-phenylene)bis(4-acetoxybenzoate)

(3,3,5-trimethylcyclohexane-1,1-diyl)bis(1,4-phenylene)bis(4-acetoxybenzoate)

Conditions
ConditionsYield
With pyridine at 110℃;89%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

1,1-bis(4-hydroxyphenyl)cyclohexane
843-55-0

1,1-bis(4-hydroxyphenyl)cyclohexane

4-(1-{4-[(4-acetoxybenzoyl)oxy]phenyl}cyclohexyl)phenyl 4-acetoxybenzoate

4-(1-{4-[(4-acetoxybenzoyl)oxy]phenyl}cyclohexyl)phenyl 4-acetoxybenzoate

Conditions
ConditionsYield
With pyridine at 110℃; Reflux;89%
With pyridine at 110℃;89%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

thiosemicarbazide
79-19-6

thiosemicarbazide

4-(2-thiocarbamoylhydrazinocarbonyl) phenyl acetate
7001-76-5

4-(2-thiocarbamoylhydrazinocarbonyl) phenyl acetate

Conditions
ConditionsYield
In tetrahydrofuran at 20℃; for 24h;89%
4-acetoxybenzoyl chloride
27914-73-4

4-acetoxybenzoyl chloride

4-methyl-2-(piperazin-1-yl)quinoline
50693-78-2

4-methyl-2-(piperazin-1-yl)quinoline

4-methyl-2-(4-(4-acetoxybenzoyl)-1-piperazinyl)-quinoline

4-methyl-2-(4-(4-acetoxybenzoyl)-1-piperazinyl)-quinoline

Conditions
ConditionsYield
Stage #1: 4-methyl-2-(piperazin-1-yl)quinoline With triethylamine In dichloromethane at 20℃; for 0.25h;
Stage #2: 4-acetoxybenzoyl chloride In dichloromethane at 20℃; for 0.25h;
88%

27914-73-4Relevant articles and documents

Selective targeting of melanoma using N-(2-diethylaminoethyl) 4-[18F]fluoroethoxy benzamide (4-[18F]FEBZA): a novel PET imaging probe

Garg, Pradeep K.,Nazih, Rachid,Wu, Yanjun,Grinevich, Vladimir P.,Garg, Sudha

, (2017)

Background: The purpose of this study was to develop a positron emission tomography (PET) imaging probe that is easy to synthesize and selectively targets melanoma in vivo. Herein, we report the synthesis and preclinical evaluation of N-(2-diethylaminoeth

Structure-Activity Study of Nitazoxanide Derivatives as Novel STAT3 Pathway Inhibitors

Lü, Zirui,Li, Xiaona,Li, Kebin,Wang, Cong,Du, Tingting,Huang, Wei,Ji, Ming,Li, Changhong,Xu, Fengrong,Xu, Ping,Niu, Yan

, p. 696 - 703 (2021/05/04)

We identified nitazoxanide (NTZ) as a moderate STAT3 pathway inhibitor through immunoblot analysis and a cell-based IL-6/JAK/STAT3 pathway activation assay. A series of thiazolide derivatives were designed and synthesized to further validate the thiazolide scaffold as STAT3 inhibitors. Eight out of 25 derivatives displayed potencies greater than that of NTZ, and their STAT3 pathway inhibitory activities were found to be significantly correlated with their antiproliferative activities in HeLa cells. Derivatives 15 and 24 were observed to be more potent than the positive control WP1066, which is under phase I clinical trials. Compared with NTZ, 15 also exhibited much improved in vivo pharmacokinetic parameters in rats and efficacies against proliferations in multiple cancer cell lines, indicating a broad-spectrum effect of these thiazolides as antitumor agents targeted on STAT3.

Synthesis and antioxidant activities of berberine 9-: O -benzoic acid derivatives

Liu, Yanfei,Long, Shuo,Zhang, Shanshan,Tan, Yifu,Wang, Ting,Wu, Yuwei,Jiang, Ting,Liu, Xiaoqin,Peng, Dongming,Liu, Zhenbao

, p. 17611 - 17621 (2021/05/29)

Although berberine (BBR) shows antioxidant activity, its activity is limited. We synthesized 9-O-benzoic acid berberine derivatives, and their antioxidant activities were screened via ABTS, DPPH, HOSC and FRAP assays. The para-position was modified with halogen elements on the benzoic acid ring, which led to an enhanced antioxidant activity and the substituent on the ortho-position was found to be better than the meta-position. Compounds 8p, 8c, 8d, 8i, 8j, 8l, and especially 8p showed significantly higher antioxidant activities, which could be attributed to the electronic donating groups. All the berberine derivatives possessed proper lipophilicities. In conclusion, compound 8p is a promising antioxidant candidate with remarkable elevated antioxidant activity and moderate lipophilicity.

Using the liquid crystalline epoxy resin thermoset aromatic diamine

-

Paragraph 0054-0055, (2020/08/26)

PROBLEM TO BE SOLVED: To provide an aromatic diamine that gives a heat-cured product useful as an electric insulation material for radiating the heat generated from a semiconductor element and the like, and a liquid crystalline epoxy resin heat-cured product prepared therewith.SOLUTION: This invention relates to an aromatic diamine represented by formula (1), and a heat-cured product of the diamine and a liquid crystalline bisepoxide represented by formula (2) (where R-Rindependently represent a hydrogen atom, a C1-C6 alkyl group or a C1-C6 alkoxy group, m is an integer of 2-14, and Xis a divalent aromatic group).SELECTED DRAWING: None

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