Product Name

  • Name

    4-Fluoro-3-phenoxybenzaldehyde

  • EINECS 269-856-2
  • CAS No. 68359-57-9
  • Article Data6
  • CAS DataBase
  • Density 1.229 g/cm3
  • Solubility
  • Melting Point
  • Formula C13H9FO2
  • Boiling Point 320 °C at 760 mmHg
  • Molecular Weight 216.212
  • Flash Point 142.5 °C
  • Transport Information UN 3082 9/PG 3
  • Appearance Light yellowish liquid.
  • Safety 61
  • Risk Codes 22-51/53
  • Molecular Structure Molecular Structure of 68359-57-9 (4-Fluoro-3-phenoxybenzaldehyde)
  • Hazard Symbols HarmfulXn; DangerousN
  • Synonyms 3-Phenoxy-4-fluorobenzaldehyde;4-Fluoro-3-phenoxybenzaldehyde;
  • PSA 26.30000
  • LogP 3.43050

Synthetic route

cyfluthrin
68359-37-5

cyfluthrin

A

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

B

3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylic acid
55701-05-8

3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylic acid

Conditions
ConditionsYield
With sodium hydroxide In methanol for 2h; Heating;
4-fluoro-3-phenoxybenzyl bromide
68359-55-7

4-fluoro-3-phenoxybenzyl bromide

1-Nitropropane
108-03-2

1-Nitropropane

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

Conditions
ConditionsYield
In ethanol
4-fluoro-3-phenoxy-benzaldehyde ethyleneacetal
77771-05-2

4-fluoro-3-phenoxy-benzaldehyde ethyleneacetal

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

Conditions
ConditionsYield
With hydrogenchloride In ethanol; water; toluene
cis-α-cyano-3-phenoxy-4-fluoro-benzyl 2,2-dimethyl-3-(2-chloro-vinyl)cyclopropanecarboxylate

cis-α-cyano-3-phenoxy-4-fluoro-benzyl 2,2-dimethyl-3-(2-chloro-vinyl)cyclopropanecarboxylate

A

3-Methylbutenoic acid
541-47-9

3-Methylbutenoic acid

B

3-(2-chloro-vinyl)-2,2-dimethylcyclopropanecarboxylic acid
60310-82-9

3-(2-chloro-vinyl)-2,2-dimethylcyclopropanecarboxylic acid

C

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

D

C8H11ClO

C8H11ClO

E

2-(4-fluoro-3-phenoxyphenyl)-2-hydroxyethanenitrile
76783-44-3

2-(4-fluoro-3-phenoxyphenyl)-2-hydroxyethanenitrile

F

4-fluoro-3-phenoxy benzoic acid
77279-89-1

4-fluoro-3-phenoxy benzoic acid

Conditions
ConditionsYield
In hexane for 17h; UV-irradiation;
4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

4-fluoro-3-phenoxy benzoic acid
77279-89-1

4-fluoro-3-phenoxy benzoic acid

Conditions
ConditionsYield
With dihydrogen peroxide; acetic acid In ethanol for 4h; Heating;100%
With potassium permanganate In water for 2h; Heating;65%
With dihydrogen peroxide; acetic acid at 60 - 80℃; for 2h;
4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

4-fluoro-3-phenoxyphenylmethanol
68359-53-5

4-fluoro-3-phenoxyphenylmethanol

Conditions
ConditionsYield
With formic acid; C20H29ClIrN4(1+)*Cl(1-) In ethanol; water at 80℃; for 0.25h; chemoselective reaction;98%
With sodium hydroxide In diethyl ether; water
With sodium hydroxide In diethyl ether; water
With sodium hydroxide In diethyl ether; water
potassium cyanide

potassium cyanide

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

C9H9Br2Cl2F3O

C9H9Br2Cl2F3O

C23H18Br2ClF4NO2

C23H18Br2ClF4NO2

Conditions
ConditionsYield
With tetrabutylammomium bromide In water; benzene at 15 - 20℃; for 10h;95%
sodium cyanide
773837-37-9

sodium cyanide

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

cis-2,2-dimethyl-3-(2-chloropropenyl)cyclopropanecarboxylic acid chloride

cis-2,2-dimethyl-3-(2-chloropropenyl)cyclopropanecarboxylic acid chloride

cis-α-cyano-4-fluoro-3-phenoxybenzyl-2,2-dimethyl-3-(2-chloropropenyl)cyclopropanecarboxylate

cis-α-cyano-4-fluoro-3-phenoxybenzyl-2,2-dimethyl-3-(2-chloropropenyl)cyclopropanecarboxylate

Conditions
ConditionsYield
With triethylamine In water; toluene at 20℃; for 4h;95%
potassium cyanide

potassium cyanide

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

(1R)-trans-2,2-dimethyl-3-(2-chloropropenyl)cyclopropanecarboxylic acid chloride

(1R)-trans-2,2-dimethyl-3-(2-chloropropenyl)cyclopropanecarboxylic acid chloride

(1R)-trans-α-cyano-4-fluoro-3-phenoxybenzyl-2,2-dimethyl-3-(2-chloropropenyl)cyclopropanecarboxylate

(1R)-trans-α-cyano-4-fluoro-3-phenoxybenzyl-2,2-dimethyl-3-(2-chloropropenyl)cyclopropanecarboxylate

Conditions
ConditionsYield
With pyridine In cyclohexane; water at 20℃; for 4h;93%
Dibenzyl phosphite
17176-77-1

Dibenzyl phosphite

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

dibenzyl α-hydroxy(4-fluoro-3-phenoxy)benzylphosphonate

dibenzyl α-hydroxy(4-fluoro-3-phenoxy)benzylphosphonate

Conditions
ConditionsYield
With triethylamine In dichloromethane at 20℃; for 14h;92%
4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

permethric acid chloride
52314-67-7

permethric acid chloride

sodium sulfate
7757-82-6

sodium sulfate

3'-phenoxy-4'-fluoro-benzyl 2,2-dimethyl-3-(2,2-dichlorovinyl)-cyclopropane-carboxylate
68359-33-1

3'-phenoxy-4'-fluoro-benzyl 2,2-dimethyl-3-(2,2-dichlorovinyl)-cyclopropane-carboxylate

Conditions
ConditionsYield
In water; ethyl acetate91.5%
4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

2-amino-N'-hydroxychroman-3-carboxamidine
1384471-91-3

2-amino-N'-hydroxychroman-3-carboxamidine

N-(4-fluoro-3-phenoxybenzylidene)-3-(5-(4-fluoro-3-phenoxyphenyl)-1,2,4-oxadiazol-3-yl)-3,4-dihydro-2H-chromen-2-amine
1384471-90-2

N-(4-fluoro-3-phenoxybenzylidene)-3-(5-(4-fluoro-3-phenoxyphenyl)-1,2,4-oxadiazol-3-yl)-3,4-dihydro-2H-chromen-2-amine

Conditions
ConditionsYield
for 0.0833333h; Irradiation;91%
sodium cyanide
773837-37-9

sodium cyanide

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

cis/trans-2,2-dimethyl-3-(2-chloropropenyl)cyclopropanecarboxylic acid chloride

cis/trans-2,2-dimethyl-3-(2-chloropropenyl)cyclopropanecarboxylic acid chloride

cis/trans-α-cyano-4-fluoro-3-phenoxybenzyl-2,2-dimethyl-3-(2-chloropropenyl)cyclopropanecarboxylate

cis/trans-α-cyano-4-fluoro-3-phenoxybenzyl-2,2-dimethyl-3-(2-chloropropenyl)cyclopropanecarboxylate

Conditions
ConditionsYield
With pyridine In cyclohexane; water at 20℃; for 4h;91%
pyridine-2,6-dicarbohydrazide
5112-36-7

pyridine-2,6-dicarbohydrazide

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

N'2,N’6-bis [(4-fluoro-3-phenoxyphenyl)methylidene]pyridine-2,6-dicarbohydrazide

N'2,N’6-bis [(4-fluoro-3-phenoxyphenyl)methylidene]pyridine-2,6-dicarbohydrazide

Conditions
ConditionsYield
With acetic acid In ethanol Reflux;89%
4-bromo-β-nitrostyrene
3156-37-4

4-bromo-β-nitrostyrene

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

β-naphthol
135-19-3

β-naphthol

C31H19BrFNO2

C31H19BrFNO2

Conditions
ConditionsYield
With ammonium acetate; sodium hydroxide In water at 80℃; for 8h; Green chemistry;87%
ethyl 4-[4-(methylthio)phenyl]-6-methyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate
292871-44-4

ethyl 4-[4-(methylthio)phenyl]-6-methyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

chloroacetic acid
79-11-8

chloroacetic acid

CH3SC6H4C6HN2SOCH3CO2CH2CH3CHC6H3FOC6H5

CH3SC6H4C6HN2SOCH3CO2CH2CH3CHC6H3FOC6H5

Conditions
ConditionsYield
With sodium acetate; acetic anhydride; acetic acid for 3h; Heating;84%
4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

toluene-4-sulfonic acid hydrazide
1576-35-8

toluene-4-sulfonic acid hydrazide

N'-[(4-fluoro-3-phenoxyphenyl)methylidene]-4-methylbenzenesulfonohydrazide

N'-[(4-fluoro-3-phenoxyphenyl)methylidene]-4-methylbenzenesulfonohydrazide

Conditions
ConditionsYield
In ethanol Reflux;84%
4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

m-tyramine
588-05-6

m-tyramine

C21H18FNO2

C21H18FNO2

Conditions
ConditionsYield
With acetic acid at 50℃; for 5h; Pictet-Spengler Synthesis; Molecular sieve; Inert atmosphere;83%
tert-butyl diethylphosphonoacetate
27784-76-5

tert-butyl diethylphosphonoacetate

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

tert-butyl (E)-3-(3'-phenoxy-4'-fluorophenyl)prop-2-enoate
1393363-56-8

tert-butyl (E)-3-(3'-phenoxy-4'-fluorophenyl)prop-2-enoate

Conditions
ConditionsYield
Stage #1: tert-butyl diethylphosphonoacetate With methylmagnesium bromide In tetrahydrofuran; diethyl ether at 20℃; for 0.25h; Inert atmosphere;
Stage #2: 4-fluoro-3-phenoxybenzaldehyde In tetrahydrofuran; diethyl ether for 15h; Horner-Wadsworth-Emmons olefination; Inert atmosphere; Reflux; optical yield given as %de; diastereoselective reaction;
82%
indole
120-72-9

indole

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

C29H21FN2O

C29H21FN2O

Conditions
ConditionsYield
With sulfated anatase titania In neat (no solvent) at 20℃; for 0.5h; Green chemistry;82%
With BiCl3-loaded montmorillonite K10 In neat (no solvent) at 20℃; for 0.666667h; Green chemistry;82%
(2-nitroethenyl)benzene
102-96-5

(2-nitroethenyl)benzene

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

malonic acid dimethyl ester
108-59-8

malonic acid dimethyl ester

6-(4-fluoro-3-phenoxyphenyl)-5-nitro-4-phenylpiperidin-2-one

6-(4-fluoro-3-phenoxyphenyl)-5-nitro-4-phenylpiperidin-2-one

Conditions
ConditionsYield
Stage #1: (2-nitroethenyl)benzene; malonic acid dimethyl ester With sodium hydroxide In methanol at 0℃; for 0.75h;
Stage #2: 4-fluoro-3-phenoxybenzaldehyde; formamide In methanol Reflux;
78%
4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

2-[3-cyano-4-(2-methylpropoxy)phenyl]-4-methyl-1,3-thiazole-5-carbohydrazide

2-[3-cyano-4-(2-methylpropoxy)phenyl]-4-methyl-1,3-thiazole-5-carbohydrazide

(E)-2-(3-cyano-4-isobutoxyphenyl)-N’-(4-fluoro-3-phenoxybenzylidene)-4-methylthiazole-5-carbohydrazide

(E)-2-(3-cyano-4-isobutoxyphenyl)-N’-(4-fluoro-3-phenoxybenzylidene)-4-methylthiazole-5-carbohydrazide

Conditions
ConditionsYield
With acetic acid In ethanol for 8h; Reflux;72%
1,5-dioxaspiro[5.5]undecane-2,4-dione
1658-27-1

1,5-dioxaspiro[5.5]undecane-2,4-dione

(2-nitroethenyl)benzene
102-96-5

(2-nitroethenyl)benzene

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

2-aza-1,3-di(4-fluoro-3-phenoxyphenyl)-4-nitro5-phenyl-8,15-dioxa-7,16-dioxodispiro[5,2,59,26]hexadecane

2-aza-1,3-di(4-fluoro-3-phenoxyphenyl)-4-nitro5-phenyl-8,15-dioxa-7,16-dioxodispiro[5,2,59,26]hexadecane

Conditions
ConditionsYield
Stage #1: 1,5-dioxaspiro[5.5]undecane-2,4-dione; (2-nitroethenyl)benzene With triethylamine In ethanol at 20℃; for 3h; Michael Addition;
Stage #2: 4-fluoro-3-phenoxybenzaldehyde With ammonium acetate In ethanol at 45℃; for 20h; Mannich Aminomethylation;
71%
4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

ethyl acetoacetate
141-97-9

ethyl acetoacetate

malononitrile
109-77-3

malononitrile

6-amino-4-(4-fluoro-3-phenoxyphenyl)-3-methyl-1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile

6-amino-4-(4-fluoro-3-phenoxyphenyl)-3-methyl-1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile

Conditions
ConditionsYield
With hydrazine hydrate; morpholine triflate In ethanol; water for 8h; Reflux; Green chemistry;67%
4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

5-amino-1-(2-hydroxy-2-phenylethyl)-1H-pyrazole-4-carbohydrazide

5-amino-1-(2-hydroxy-2-phenylethyl)-1H-pyrazole-4-carbohydrazide

(E)-5-amino-1-(2-hydroxy-2-phenylethyl)-N’-(4-fluoro-3-phenoxybenzylidene)-1H-pyrazole-4-carbohydrazide

(E)-5-amino-1-(2-hydroxy-2-phenylethyl)-N’-(4-fluoro-3-phenoxybenzylidene)-1H-pyrazole-4-carbohydrazide

Conditions
ConditionsYield
In methanol; ethanol at 100℃; for 18h;65%
1-methoxy-4-(2-nitro-vinyl)-benzene
3179-10-0

1-methoxy-4-(2-nitro-vinyl)-benzene

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

malonic acid dimethyl ester
108-59-8

malonic acid dimethyl ester

6-(4-fluoro-3-phenoxyphenyl)-4-(4-methoxyphenyl)-5-nitropiperidin-2-one

6-(4-fluoro-3-phenoxyphenyl)-4-(4-methoxyphenyl)-5-nitropiperidin-2-one

Conditions
ConditionsYield
Stage #1: 1-methoxy-4-(2-nitro-vinyl)-benzene; malonic acid dimethyl ester With sodium hydroxide In methanol at 0℃; for 0.75h;
Stage #2: 4-fluoro-3-phenoxybenzaldehyde; formamide In methanol Reflux;
63%
4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

2-amino-4,6-di-tertbutylphenol
1643-39-6

2-amino-4,6-di-tertbutylphenol

2,4-di-tert-butyl-6-{[(4-fluoro-3-phenoxyphenyl)methylene]amino}phenol

2,4-di-tert-butyl-6-{[(4-fluoro-3-phenoxyphenyl)methylene]amino}phenol

Conditions
ConditionsYield
for 2h; Heating;62%
1-methoxy-4-(2-nitro-vinyl)-benzene
3179-10-0

1-methoxy-4-(2-nitro-vinyl)-benzene

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

1,3-cylohexanedione
504-02-9

1,3-cylohexanedione

2-(4-fluoro-3-phenoxybenzylideneamino)-3-(4-methoxyphenyl)benzofuran-4-ol

2-(4-fluoro-3-phenoxybenzylideneamino)-3-(4-methoxyphenyl)benzofuran-4-ol

Conditions
ConditionsYield
With piperidine; ammonium acetate In N,N-dimethyl-formamide at 20℃; for 7h; Michael Addition; Reflux;61%
4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

3-(4-Ethoxyphenyl)-3-methyl-2-butanone
89765-17-3

3-(4-Ethoxyphenyl)-3-methyl-2-butanone

1-(4-Fluoro-3-phenoxyphenyl)-4-(4-ethoxyphenyl)-4-methylpent-1-ene-3-one
89765-18-4

1-(4-Fluoro-3-phenoxyphenyl)-4-(4-ethoxyphenyl)-4-methylpent-1-ene-3-one

Conditions
ConditionsYield
With potassium hydroxide In ethanol at 20℃; for 6h; Condensation;60%
4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

ethyltriphenylphosphonium bromide
1530-32-1

ethyltriphenylphosphonium bromide

(E)-1-fluoro-2-phenoxy-4-(prop-1-en-1-yl)benzene

(E)-1-fluoro-2-phenoxy-4-(prop-1-en-1-yl)benzene

Conditions
ConditionsYield
With potassium carbonate In 1,4-dioxane at 110℃;56.8%
cycl-isopropylidene malonate
2033-24-1

cycl-isopropylidene malonate

1-methoxy-4-(2-nitro-vinyl)-benzene
3179-10-0

1-methoxy-4-(2-nitro-vinyl)-benzene

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

8-aza-7,9-di(4-fluoro-3-phenoxyphenyl)-11-(p-methoxyphenyl)-3,3-dimethyl-10-nitro-2,4-dioxa-1,5-dioxospiro[5,5]undecane

8-aza-7,9-di(4-fluoro-3-phenoxyphenyl)-11-(p-methoxyphenyl)-3,3-dimethyl-10-nitro-2,4-dioxa-1,5-dioxospiro[5,5]undecane

Conditions
ConditionsYield
Stage #1: cycl-isopropylidene malonate; 1-methoxy-4-(2-nitro-vinyl)-benzene With triethylamine In ethanol at 20℃; for 3h; Michael Addition;
Stage #2: 4-fluoro-3-phenoxybenzaldehyde With ammonium acetate In ethanol at 45℃; for 20h; Mannich Aminomethylation;
55%
o-(chloromethyl)benzoic acid methyl ester
34040-62-5

o-(chloromethyl)benzoic acid methyl ester

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

3-(4-fluoro-3-phenoxyphenyl)-3,4-dihydroisocoumarin

3-(4-fluoro-3-phenoxyphenyl)-3,4-dihydroisocoumarin

Conditions
ConditionsYield
With N1,N1,N12,N12-tetramethyl-7,8-dihydro-6H-dipyrido[1,2-a:2,1'-c][1,4]diazepine-2,12-diamine In N,N-dimethyl-formamide at 20℃; for 16h; Glovebox; Inert atmosphere;55%
(E)-1-methoxy-4-(2-nitrovinyl)benzene
3179-10-0, 5576-97-6

(E)-1-methoxy-4-(2-nitrovinyl)benzene

4-fluoro-3-phenoxybenzaldehyde
68359-57-9

4-fluoro-3-phenoxybenzaldehyde

malonic acid dimethyl ester
108-59-8

malonic acid dimethyl ester

C26H23FN2O7

C26H23FN2O7

Conditions
ConditionsYield
Stage #1: (E)-1-methoxy-4-(2-nitrovinyl)benzene; malonic acid dimethyl ester With sodium hydroxide In methanol at 0℃; for 0.75h;
Stage #2: 4-fluoro-3-phenoxybenzaldehyde With ammonium acetate In methanol at 20 - 85℃; for 40h;
53%

4-Fluoro-3-phenoxybenzaldehyde Chemical Properties

IUPAC Name: 4-Fluoro-3-phenoxybenzaldehyde 
Following is the structure of Benzaldehyde,4-fluoro-3-phenoxy- (CAS NO.68359-57-9):
                    
Empirical Formula: C13H9FO2
Molecular Weight: 216.2078 
EINECS: 269-856-2
Index of Refraction: 1.591
Molar Refractivity: 59.44 cm3
Molar Volume: 175.8 cm3
Polarizability: 23.56 10-24cm3
Surface Tension: 43 dyne/cm
Density: 1.229 g/cm3
Flash Point: 142.5 °C
Enthalpy of Vaporization: 56.16 kJ/mol
Boiling Point: 320 °C at 760 mmHg
Vapour Pressure: 0.000327 mmHg at 25 °C 
Product Categories: Aromatic Aldehydes & Derivatives (substituted);Aldehydes;C10 to C21;Carbonyl Compounds
Canonical SMILES: C1=CC=C(C=C1)OC2=C(C=CC(=C2)C=O)F
InChI: InChI=1S/C13H9FO2/c14-12-7-6-10(9-15)8-13(12)16-11-4-2-1-3-5-11/h1-9H
InChIKey: JDICMOLUAHZVDS-UHFFFAOYSA-N

4-Fluoro-3-phenoxybenzaldehyde Safety Profile

Hazard Codes: HarmfulXn,DangerousN
Risk Statements: 22-51/53 
R22:Harmful if swallowed. 
R51/53:Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment.
Safety Statements: 61 
S61:Avoid release to the environment. Refer to special instructions / safety data sheets.
RIDADR UN: 3082 9/PG 3
WGK Germany: 2
Hazard Note: Harmful

4-Fluoro-3-phenoxybenzaldehyde Specification

 Benzaldehyde,4-fluoro-3-phenoxy- , its cas register number 68359-57-9. It also can be called 3-(Phenoxy)-4-fluoro-benzaldehyde ; and 4-Fluoro-3-phenoxybenzaldehyde .

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