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618-95-1 Usage

Chemical Properties

beige crystalline powder

Uses

Methyl 3-nitrobenzoate was used in the preparation of iodoarene.

Synthesis Reference(s)

Synthetic Communications, 22, p. 1851, 1992 DOI: 10.1080/00397919208021316Chemical and Pharmaceutical Bulletin, 36, p. 481, 1988 DOI: 10.1248/cpb.36.481

Purification Methods

Crystallise the benzoate from MeOH (1g/mL). [Beilstein 9 H 378, 9 I 153, 9 II 248, 9 III 1493, 9 IV 1056.]

Check Digit Verification of cas no

The CAS Registry Mumber 618-95-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 618-95:
(5*6)+(4*1)+(3*8)+(2*9)+(1*5)=81
81 % 10 = 1
So 618-95-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H7NO4/c1-13-8(10)6-3-2-4-7(5-6)9(11)12/h2-5H,1H3

618-95-1 Well-known Company Product Price

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  • Alfa Aesar

  • (A15155)  Methyl 3-nitrobenzoate, 98+%   

  • 618-95-1

  • 50g

  • 205.0CNY

  • Detail
  • Alfa Aesar

  • (A15155)  Methyl 3-nitrobenzoate, 98+%   

  • 618-95-1

  • 250g

  • 841.0CNY

  • Detail
  • Alfa Aesar

  • (A15155)  Methyl 3-nitrobenzoate, 98+%   

  • 618-95-1

  • 1000g

  • 3276.0CNY

  • Detail

618-95-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3-nitrobenzoate

1.2 Other means of identification

Product number -
Other names Benzoic acid,3-nitro-,methyl ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:618-95-1 SDS

618-95-1Synthetic route

methanol
67-56-1

methanol

3-nitro-benzaldehyde
99-61-6

3-nitro-benzaldehyde

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With 1-(ferrocenylbutyl)-4-(3-methylimidazolium) tetrafluoroborate; iodine; potassium carbonate at 50 - 60℃; for 24h; Inert atmosphere;100%
With palladium 10% on activated carbon; oxygen; sodium carbonate at 90℃; under 15001.5 Torr; for 2h; Microwave irradiation; Green chemistry;98%
With 3-(7,7-dimethyl-2-oxobicyclo[2.2.1]hept-1-yl)methyl-1-(2,4,6-trimethylphenyl)-1H-imidazol-3-ium bis(trifluoromethanesulfonimide) salt; caesium carbonate In toluene at 60℃; for 3h;98%
3-nitrobenzoic acid
121-92-6

3-nitrobenzoic acid

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
In 2-methyltetrahydrofuran; diethyl ether at 20℃; for 0.486667h; Flow reactor;99%
With diethyl ether
In diethyl ether
at 0℃; for 0.25h;62.3 mg
methanol
67-56-1

methanol

3-nitrobenzoic acid
121-92-6

3-nitrobenzoic acid

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With 4-methyl-morpholine; 2-chloro-4-methoxy-6-(N-phenylbenzamido)-1,3,5-triazine at 20℃; for 1h;99%
With oxone at 65℃; for 30h;98%
Stage #1: 3-nitrobenzoic acid With oxalyl dichloride; N,N-dimethyl-formamide In dichloromethane at 20℃;
Stage #2: methanol In dichloromethane for 0.0833333h;
98%
methanol
67-56-1

methanol

m-iodonitrobenzene
645-00-1

m-iodonitrobenzene

carbon monoxide
201230-82-2

carbon monoxide

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With triethylamine at 100℃; under 3750.38 Torr; for 1.5h; Inert atmosphere;99%
methanol
67-56-1

methanol

3-nitrophenylglyoxal
6890-77-3

3-nitrophenylglyoxal

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With oxone at 65℃; for 30h;99%
3-nitrobenzoic acid
121-92-6

3-nitrobenzoic acid

methyl iodide
74-88-4

methyl iodide

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With potassium hydroxide In dimethyl sulfoxide at 20℃; for 2h;98%
In acetonitrile for 8h; Inert atmosphere; Alkaline conditions;
methanol
67-56-1

methanol

3-Nitrobenzyl alcohol
619-25-0

3-Nitrobenzyl alcohol

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With sodium carbonate; palladium; silver(l) oxide at 80℃; for 48h; Molecular sieve;98%
Stage #1: 3-Nitrobenzyl alcohol In toluene at 80℃; for 2h; Sonication;
Stage #2: methanol With Oxone In toluene for 1.5h; Sonication;
90%
With dibromamine-T; potassium carbonate In acetonitrile at 20℃; for 0.5h; Reagent/catalyst; Solvent;88%
methanol
67-56-1

methanol

2-(3-nitrophenyl)-2-oxoacetic acid
6330-40-1

2-(3-nitrophenyl)-2-oxoacetic acid

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With oxone at 65℃; for 30h;98%
methanol
67-56-1

methanol

methyl 2-(3-nitrophenyl)-2-oxoacetate
149621-25-0

methyl 2-(3-nitrophenyl)-2-oxoacetate

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With oxone at 65℃; for 30h;95%
dimethyl sulfate
77-78-1

dimethyl sulfate

3-nitrobenzoic acid
121-92-6

3-nitrobenzoic acid

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
Stage #1: 3-nitrobenzoic acid With potassium carbonate In acetone for 0.5h;
Stage #2: dimethyl sulfate In acetone at 20℃; for 2h;
94.3%
benzoic acid methyl ester
93-58-3

benzoic acid methyl ester

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With trifluoromethylsulfonic anhydride; ethylammonium nitrate at -5 - 20℃; for 2h; Inert atmosphere; regioselective reaction;94%
With sulfuric acid; guanidine nitrate at 0 - 5℃; for 3h;76%
With boron trifluoride; nitric acid
carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

3-nitrobenzoic acid
121-92-6

3-nitrobenzoic acid

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With 1,8-diazabicyclo[5.4.0]undec-7-ene In N,N-dimethyl-formamide for 0.0166667h; microwave irradiation;94%
With layered double hydroxide - supported L-methionine at 180℃; for 6h; Autoclave; chemoselective reaction;89%
3-nitrobenzoic acid
121-92-6

3-nitrobenzoic acid

methyl salicylate
119-36-8

methyl salicylate

A

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

B

salicylic acid
69-72-7

salicylic acid

Conditions
ConditionsYield
Stage #1: 3-nitrobenzoic acid With potassium carbonate In N,N-dimethyl acetamide at 110℃; for 0.5h;
Stage #2: methyl salicylate at 110℃; for 24h;
A 93%
B n/a
(4-(methoxycarbonyl)-2-nitrophenyl)boronic acid
85107-55-7

(4-(methoxycarbonyl)-2-nitrophenyl)boronic acid

A

dimethyl 2,2’-dinitro-[1,1’-biphenyl]-4,4’-dicarboxylate
65235-35-0

dimethyl 2,2’-dinitro-[1,1’-biphenyl]-4,4’-dicarboxylate

B

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With tris-(dibenzylideneacetone)dipalladium(0); potassium fluoride dihydrate; tri tert-butylphosphoniumtetrafluoroborate In tetrahydrofuran for 1h; Suzuki-Miyaura Coupling; Inert atmosphere; Reflux; Schlenk technique;A 10%
B 88%
methanol
67-56-1

methanol

3'-nitropropiophenone
17408-16-1

3'-nitropropiophenone

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With N,N-dimethyl-formamide dimethyl acetal for 16h; Heating;87%
3-nitrobenzoic acid
121-92-6

3-nitrobenzoic acid

diazomethyl-trimethyl-silane
18107-18-1

diazomethyl-trimethyl-silane

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
In methanol; toluene at 20℃; for 1.5h;87%
In methanol; toluene at 20℃; for 1.5h;86.79%
methyl 2-iodo-3-nitrobenzoate
93415-79-3

methyl 2-iodo-3-nitrobenzoate

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With air; tributyl borane; water In benzene at 20℃;85%
methanol
67-56-1

methanol

1-(3-nitrophenyl)-1-butanone
50766-86-4

1-(3-nitrophenyl)-1-butanone

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With N,N-dimethyl-formamide dimethyl acetal for 16h; Heating;84%
tris(o-methoxyphenyl)phosphine
4731-65-1

tris(o-methoxyphenyl)phosphine

3-nitrobenzoic acid
121-92-6

3-nitrobenzoic acid

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With dirhodium tetraacetate In cyclohexane at 120℃; for 12h; Schlenk technique; Inert atmosphere;81%
methanol
67-56-1

methanol

3-nitrobenzaldoxime
3431-62-7

3-nitrobenzaldoxime

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With 2-nitrobenzeneseleninic acid; dihydrogen peroxide at 20℃; for 48h;80%
methyl 2-iodo-3-nitrobenzoate
93415-79-3

methyl 2-iodo-3-nitrobenzoate

phenylacetylene
536-74-3

phenylacetylene

A

methyl 3-nitro-2-(2-phenylethynyl)benzoate
894854-29-6

methyl 3-nitro-2-(2-phenylethynyl)benzoate

B

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With copper(l) iodide; diisopropylamine; bis-triphenylphosphine-palladium(II) chloride In tetrahydrofuran at 45℃; for 48h; Sonogashira coupling;A 80%
B 28%
trimethoxysilane
2487-90-3

trimethoxysilane

(3-nitrophenyl)acetonitrile
621-50-1

(3-nitrophenyl)acetonitrile

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With pyridine; ferric(III) bromide; oxygen In chlorobenzene at 130℃; for 9h; Sealed tube;80%
methanol
67-56-1

methanol

3-nitrobenzaldehyde O-methyl oxime
33499-33-1

3-nitrobenzaldehyde O-methyl oxime

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With 2-nitrobenzeneseleninic acid; dihydrogen peroxide at 65℃; for 48h;79%
[3-(methoxycarbonyl)phenyl]boronic acid
99769-19-4

[3-(methoxycarbonyl)phenyl]boronic acid

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With Iron(III) nitrate nonahydrate In toluene at 80℃; for 18h; Inert atmosphere;78%
Multi-step reaction with 2 steps
1.1: potassium hydrogen bifluoride / methanol; water / 0.03 h / 0 - 20 °C / Inert atmosphere
1.2: 0.02 h / 20 °C
2.1: Oxone / water; acetone / 2 h / 60 °C
View Scheme
(E,E)-1-(N,N-dimethylamino)-4-nitro-1,3-butadiene
108030-46-2

(E,E)-1-(N,N-dimethylamino)-4-nitro-1,3-butadiene

propynoic acid methyl ester
922-67-8

propynoic acid methyl ester

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
In xylene for 8h; Heating;74.8%
methanol
67-56-1

methanol

3-nitro-benzaldehyde
99-61-6

3-nitro-benzaldehyde

A

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

B

3-nitrobenzoic acid
121-92-6

3-nitrobenzoic acid

Conditions
ConditionsYield
With dihydrogen peroxide; calcium chloride at 65℃; for 48h; Reagent/catalyst;A 74%
B n/a
With dihydrogen peroxide at 20 - 70℃; for 15h; Green chemistry;A 68%
B 31%
With dihydrogen peroxide at 20℃; for 8h;
propan-1-ol
71-23-8

propan-1-ol

3-nitro-benzaldehyde
99-61-6

3-nitro-benzaldehyde

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
Stage #1: propan-1-ol; 3-nitro-benzaldehyde With sodium hypochlorite; sodium iodide In water for 0.166667h; Cooling with ice;
Stage #2: With sodium hypochlorite In water for 1.33333h; Cooling with ice;
74%
methanol
67-56-1

methanol

2-nitro-1-(3-nitrophenyl)ethan-1-one
14367-80-7

2-nitro-1-(3-nitrophenyl)ethan-1-one

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With potassium carbonate at 80℃; for 2h; Schlenk technique; Inert atmosphere;74%
With potassium carbonate at 80℃; for 2h; Inert atmosphere; Sealed tube;74%
Trimethyl borate
121-43-7

Trimethyl borate

(3-nitrophenyl)acetonitrile
621-50-1

(3-nitrophenyl)acetonitrile

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With pyridine; ferric(III) bromide; oxygen In chlorobenzene at 130℃; for 9h; Sealed tube;74%
methanol
67-56-1

methanol

CYANAMID
420-04-2

CYANAMID

3-nitro-benzaldehyde
99-61-6

3-nitro-benzaldehyde

A

methyl N-cyano-3-nitrobenzimidate
1196908-12-9

methyl N-cyano-3-nitrobenzimidate

B

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Conditions
ConditionsYield
With N-Bromosuccinimide; sodium t-butanolate at 50℃; for 12h;A 72%
B 16%
methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

Methyl 3-aminobenzoate
4518-10-9

Methyl 3-aminobenzoate

Conditions
ConditionsYield
With potassium fluoride; polymethylhydrosiloxane; palladium diacetate In tetrahydrofuran; water at 20℃; for 0.5h;100%
With potassium fluoride; polymethylhydrosiloxane; palladium diacetate In tetrahydrofuran at 20℃; for 0.5h;100%
With 5%-palladium/activated carbon; hydrogen In methanol at 20℃;100%
methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

methyl 3-(hydroxylamino)benzoate
36475-13-5

methyl 3-(hydroxylamino)benzoate

Conditions
ConditionsYield
With 5% Rh/C; hydrazine hydrate In tetrahydrofuran at 0℃; Inert atmosphere; Schlenk technique; Sealed tube;100%
With 5% rhodium-on-charcoal; hydrazine hydrate In tetrahydrofuran at 0℃; for 2.5h; Inert atmosphere;99%
With 5% rhodium-on-charcoal; hydrazine hydrate In tetrahydrofuran at 0℃; Inert atmosphere;99%
methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

ethylenediamine
107-15-3

ethylenediamine

2-(3-nitrophenyl)-2-imidazoline
31659-42-4

2-(3-nitrophenyl)-2-imidazoline

Conditions
ConditionsYield
With sulfur In methanol at 65℃; for 5h; Time;96.4%
methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

3-nitrobenzoic acid hydrazide
618-94-0

3-nitrobenzoic acid hydrazide

Conditions
ConditionsYield
With hydrazine hydrate In ethanol for 4h; Reflux;96%
With hydrazine hydrate In ethanol at 85℃; for 4h;96.2%
With hydrazine hydrate In ethanol for 0.2h; Reflux; Microwave irradiation;95%
methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

sodium 4-methylbenzenesulfinate
824-79-3

sodium 4-methylbenzenesulfinate

methyl 3-{[(4-methylphenyl)sulfonyl]amino}benzoate
173436-66-3

methyl 3-{[(4-methylphenyl)sulfonyl]amino}benzoate

Conditions
ConditionsYield
With trans-N,N'-dimethyl-1,2-cyclohexyldiamine; sodium hydrogen sulfite; iron(II) chloride In dimethyl sulfoxide at 60℃; for 12h; Sealed tube; Inert atmosphere;95%
With sodium hydrogensulfite In water at 60℃; for 20h; chemoselective reaction;86%
methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

3-nitro benzhydroxamic acid
7335-34-4

3-nitro benzhydroxamic acid

Conditions
ConditionsYield
With hydroxylamine hydrochloride; sodium hydroxide In methanol at 20℃; pH=> 10;93%
methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

3-nitrobenzamide
645-09-0

3-nitrobenzamide

Conditions
ConditionsYield
Stage #1: methyl 3-nitrobenzoate With ammonia In ethylene glycol at 40 - 45℃; for 20h;
Stage #2: sodium methylate In ethylene glycol at 40 - 45℃; for 5h; Conversion of starting material;
92%
With ammonia; sodium methylate In methanol at 60 - 65℃; for 26h; Conversion of starting material;68%
Stage #1: methyl 3-nitrobenzoate With ammonia In butan-1-ol at 40 - 45℃; for 20h;
Stage #2: sodium methylate In butan-1-ol at 40 - 45℃; for 8h; Conversion of starting material;
phenyl benzyl ketone
451-40-1

phenyl benzyl ketone

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

C22H18O3

C22H18O3

Conditions
ConditionsYield
With potassium phosphate; bis(acetylacetonato)palladium(II); dicyclohexyl-(2′,4′,6′-triisopropyl-3,6-dimethoxy-[1,1′-biphenyl]-2-yl)phosphine In cyclohexane at 130℃; for 24h; Inert atmosphere;92%
methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

3-Nitrobenzyl alcohol
619-25-0

3-Nitrobenzyl alcohol

Conditions
ConditionsYield
With sodium tetrahydroborate; ethanol; cerium(III) chloride heptahydrate at 20℃; for 24h; chemospecific reaction;91%
With sodium tetrahydroborate; zinc phthalocyanine In PEG-400 at 100℃; for 10h;90%
With sodium tetrahydroborate In 1,4-dioxane; water for 2h; Ambient temperature;80%
1-Bromo-2,4-dimethoxybenzene
17715-69-4

1-Bromo-2,4-dimethoxybenzene

methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

2,2',4,4'-tetramethoxy-3''-nitrotrityl alcohol
864745-95-9

2,2',4,4'-tetramethoxy-3''-nitrotrityl alcohol

Conditions
ConditionsYield
Stage #1: 1-Bromo-2,4-dimethoxybenzene With iodine; magnesium In tetrahydrofuran for 0.333333h;
Stage #2: methyl 3-nitrobenzoate In tetrahydrofuran at -78℃;
91%
methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

methyl 3-bromo-5-nitrobenzoate
6307-87-5

methyl 3-bromo-5-nitrobenzoate

Conditions
ConditionsYield
With sulfuric acid; dibromoisocyanuric acid90%
With sulfuric acid; dibromoisocyanuric acid at 20℃; for 2h;86%
With sulfuric acid; dibromoisocyanuric acid at 20℃; for 2h; Inert atmosphere; Schlenk technique;86%
methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

5-nitrosalicylic acid
96-97-9

5-nitrosalicylic acid

Conditions
ConditionsYield
With potassium hydroxide; Cumene hydroperoxide In ammonia at -33℃;90%
methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

propan-1-ol-3-amine
156-87-6

propan-1-ol-3-amine

N-(3-Hydroxypropyl)-3-nitrobenzamide
254454-76-7

N-(3-Hydroxypropyl)-3-nitrobenzamide

Conditions
ConditionsYield
In toluene at 94℃; for 3.5h; Acylation;90%
methyl 3-nitrobenzoate
618-95-1

methyl 3-nitrobenzoate

tert-butyl alcohol
75-65-0

tert-butyl alcohol

3-nitro-benzoic acid t-butyl ester
58656-99-8

3-nitro-benzoic acid t-butyl ester

Conditions
ConditionsYield
With n-butyllithium In tetrahydrofuran; hexane for 1h;89%

618-95-1Relevant articles and documents

Light-induced carboxylation of aryl derivatives with cooperative COF as an active photocatalyst and Ni(ii) co-catalyst

Chakrabortty, Pekham,Das, Anjan,Chowdhury, Arpita Hazra,Ghosh, Swarbhanu,Khan, Aslam,Islam, Sk. Manirul

, p. 4738 - 4745 (2021/03/22)

The photocatalytic carboxylation of aryl derivatives was demonstrated under CO2at atmospheric pressure using a mesoporous covalent organic framework (COF) as the active photocatalyst with triethylamine (TEA) as a sacrificial electron source under visible light. A yield of greater than 91% of the isolated product was achieved with 5 mg of catalyst. The reaction cycle is dependent on the use of the Ni(dmg)2co-catalyst and the sacrificial electron donor (TEA). The reaction does not occur in the absence of light (445 nm) even at elevated reaction temperature. We have also demonstrated that a yield of 32% of the isolated product could be obtained with the use of sunlight in the catalytic cycle. Additionally, this heterogeneous catalytic system was recyclable and reusable for several cycles.

Indolone derivative and pharmaceutical application thereof

-

Paragraph 0040-0046, (2021/03/31)

The invention provides an indolone derivative and pharmaceutical application thereof. The structure of the indolone derivative is shown as a formula (A). Experimental results show that the compound provided by the invention has obviously improved pharmacokinetic properties than BIBF1120, has excellent inhibition effects on VEGFR, FGFR and PDGFR, can be used as a VEGFR, FGFR and/or PDGFR inhibitor,an angiogenesis inhibitor and a drug for preventing and/or treating various tumors including pharyngeal squamous cell carcinoma, and has a wide application prospect.

Antibacterial and Antiviral Activities of 1,3,4-Oxadiazole Thioether 4H-Chromen-4-one Derivatives

Cao, Xiao,Liu, Fang,Liu, Liwei,Liu, Tingting,Peng, Feng,Wang, Qifan,Xie, Chengwei,Xue, Wei,Yang, Jinsong

, p. 11085 - 11094 (2021/10/01)

Various 1,3,4-oxadiazole thioether 4H-chromen-4-one derivatives were conceived. The title compounds demonstrated striking inhibitory effects againstXac,Psa, andXoo. EC50data exhibited that A8 (19.7 μg/mL) had better antibacterial activity againstXoothan myricetin, BT, and TC. Simultaneously, the mechanism of action of A8 had been verified by SEM. The results of anti-tobacco mosaic virus indicated that A9 had the bestin vivoantiviral effect compared with ningnanmycin. From the data of MST, it could be seen that A9 (0.003 ± 0.001 μmol/L) exhibited a strong binding capacity, which was far superior to ningnanmycin (2.726 ± 1.301 μmol/L). This study shows that the 1,3,4-oxadiazole thioether 4H-chromen-4-one derivatives may become agricultural drugs with great potential.

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