Product Name

  • Name

    3,5-Dichlorobenzaldehyde

  • EINECS 233-499-0
  • CAS No. 10203-08-4
  • Article Data18
  • CAS DataBase
  • Density 1.4 g/cm3
  • Solubility Insoluble in water.
  • Melting Point 63.5-65.5 °C(lit.)
  • Formula C7H4Cl2O
  • Boiling Point 241.1 °C at 760 mmHg
  • Molecular Weight 175.014
  • Flash Point 98.3 °C
  • Transport Information UN 3261 8/PG 2
  • Appearance white to slightly yellow fluffy powder
  • Safety 26-36/37/39-45-22-37/39
  • Risk Codes 34-36/37/38-22
  • Molecular Structure Molecular Structure of 10203-08-4 (3,5-Dichlorobenzaldehyde)
  • Hazard Symbols CorrosiveC,IrritantXi,HarmfulXn
  • Synonyms NSC 109095;
  • PSA 17.07000
  • LogP 2.80590

Synthetic route

3,5-dichloro-N,N-diethylbenzamide
35515-07-2

3,5-dichloro-N,N-diethylbenzamide

3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

Conditions
ConditionsYield
With Schwartz's reagent In tetrahydrofuran at 20℃; for 0.5h;82%
3,5-dichlorobenzaldehyde oxime
93033-57-9

3,5-dichlorobenzaldehyde oxime

3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

Conditions
ConditionsYield
With potassium sulfate; potassium hydrogensulfate; potassium peroxomonosulfate; acetic acid In water at 40 - 45℃; for 3.5h;80%
3,5-dichlorotoluene
25186-47-4

3,5-dichlorotoluene

3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

Conditions
ConditionsYield
With sodium molybdate; dihydrogen peroxide; cobalt(II) acetate; acetic acid; sodium bromide at 105℃; for 0.166667h; Temperature;39.2%
3,5-dichlorobenzyl alcohol
60211-57-6

3,5-dichlorobenzyl alcohol

3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

Conditions
ConditionsYield
With pyridinium chlorochromate In dichloromethane
With potassium fluoride; 2-fluoropyridine; silver trifluoromethanesulfonate; (trifluoromethyl)trimethylsilane; Selectfluor In ethyl acetate at 20℃; for 12h; Glovebox; Inert atmosphere;
3,5-dichlorobenzoyl chloride
2905-62-6

3,5-dichlorobenzoyl chloride

3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

Conditions
ConditionsYield
With lithium tri-t-butoxyaluminum hydride In diethylene glycol dimethyl ether
Multi-step reaction with 2 steps
1: dichloromethane / 0.5 h / 20 °C / Cooling with ice
2: Schwartz's reagent / tetrahydrofuran / 0.5 h / 20 °C
View Scheme
sulfuric acid
7664-93-9

sulfuric acid

1,3-dichloro-5-dichloromethyl-benzene
56961-85-4

1,3-dichloro-5-dichloromethyl-benzene

3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

Conditions
ConditionsYield
at 0℃;
3.5-dichloro-benzylidene dibromide

3.5-dichloro-benzylidene dibromide

3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

Conditions
ConditionsYield
With sulfuric acid at 80 - 85℃;
3.5-dichloro-benzylidene dichloride

3.5-dichloro-benzylidene dichloride

3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

Conditions
ConditionsYield
With sulfuric acid at 0℃;
formaldoxime
75-17-2

formaldoxime

diazotized.3,5-dichloro-aniline

diazotized.3,5-dichloro-aniline

3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

Conditions
ConditionsYield
anschliessenden Erhitzen mit wss.HCl;
diazotized.4-amino-3,5-dichloro-benzaldehyde

diazotized.4-amino-3,5-dichloro-benzaldehyde

3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

Conditions
ConditionsYield
With hydrogenchloride
water
7732-18-5

water

(3,5-dichloro-phenyl)-hydroxy-methanesulfonic acid ; sodium-salt

(3,5-dichloro-phenyl)-hydroxy-methanesulfonic acid ; sodium-salt

3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

3,5-dichlorobenzoic acid
51-36-5

3,5-dichlorobenzoic acid

3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: SOCl2
2: Li / bis-(2-methoxy-ethyl) ether
View Scheme
Multi-step reaction with 2 steps
1.1: thionyl chloride / toluene / 4 h / Reflux
1.2: 6.5 h / 0 - 20 °C
2.1: sodium bis(2-methoxyethoxy)aluminium dihydride / toluene / 1 h / -20 - -10 °C
View Scheme
2,4-dichlorobenzoyl chloride
89-75-8

2,4-dichlorobenzoyl chloride

3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

Conditions
ConditionsYield
With triethylsilane; bis-triphenylphosphine-palladium(II) chloride; (Z)-N,N-diisopropyl-2-styrylbenzamide In tetrahydrofuran at 65℃; for 24h; Inert atmosphere; chemoselective reaction;
3,5-dichloro-N-methoxy-N-methylbenzamide
259796-12-8

3,5-dichloro-N-methoxy-N-methylbenzamide

3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

Conditions
ConditionsYield
With sodium bis(2-methoxyethoxy)aluminium dihydride In toluene at -20 - -10℃; for 1h; Temperature;
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

2,2-dimethoxyethylamine
22483-09-6

2,2-dimethoxyethylamine

[1-(3,5-Dichloro-phenyl)-meth-(Z)-ylidene]-(2,2-dimethoxy-ethyl)-amine

[1-(3,5-Dichloro-phenyl)-meth-(Z)-ylidene]-(2,2-dimethoxy-ethyl)-amine

Conditions
ConditionsYield
In benzene Heating;100%
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

2,2-diethoxy-ethanamine
645-36-3

2,2-diethoxy-ethanamine

(3,5-dichloro-benzylidene)-(2,2-diethoxy-ethyl)-amine
1000210-73-0

(3,5-dichloro-benzylidene)-(2,2-diethoxy-ethyl)-amine

Conditions
ConditionsYield
In toluene for 2.5h; Reflux;100%
In ethanol at 20 - 78℃; for 2h;94%
In ethanol at 20℃; for 8h;70.68%
In ethanol at 75℃; for 3h; Temperature;125 g
3,5-dimethyl-4-nitroisoxazole
1123-49-5

3,5-dimethyl-4-nitroisoxazole

3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

5-[(E)-2-(3,5-Dichloro-phenyl)-vinyl]-3-methyl-4-nitro-isoxazole

5-[(E)-2-(3,5-Dichloro-phenyl)-vinyl]-3-methyl-4-nitro-isoxazole

Conditions
ConditionsYield
With pyrrolidine In neat (no solvent) at 20℃; for 0.05h; Aldol Condensation;100%
With piperidine In acetonitrile for 4h; Knoevenagel condensation; Reflux;
5,6-dihydro-4H-benzo[f][1,2,3]triazolo[1,5-a][1,4]diazepine

5,6-dihydro-4H-benzo[f][1,2,3]triazolo[1,5-a][1,4]diazepine

3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

C17H14Cl2N4
1358787-23-1

C17H14Cl2N4

Conditions
ConditionsYield
With sodium tris(acetoxy)borohydride; acetic acid In 1,2-dichloro-ethane100%
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

C7H5Cl2NO

C7H5Cl2NO

Conditions
ConditionsYield
Stage #1: 3,5-dichlorobenzaldehyde With sodium hydroxide; hydroxylamine hydrochloride In ethanol; water at 4 - 20℃; for 3h;
Stage #2: pH=6; Acidic aqueous solution;
99%
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

3,5-dichlorobenzaldehyde oxime
93033-57-9

3,5-dichlorobenzaldehyde oxime

Conditions
ConditionsYield
With hydroxylamine hydrochloride; sodium acetate In ethanol for 2.5h;98%
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

2,6-dichloro-p-phenylenediamine
609-20-1

2,6-dichloro-p-phenylenediamine

2,6-Dichloro-N'-[1-(3,5-dichloro-phenyl)-meth-(E)-ylidene]-benzene-1,4-diamine
84562-37-8

2,6-Dichloro-N'-[1-(3,5-dichloro-phenyl)-meth-(E)-ylidene]-benzene-1,4-diamine

Conditions
ConditionsYield
In ethanol for 1.5h; Heating;98%
tert-butyl (2S)-2-[(isobutylamino)methyl]pyrrolidine-1-carboxylate
871499-96-6

tert-butyl (2S)-2-[(isobutylamino)methyl]pyrrolidine-1-carboxylate

3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

tert-butyl (2S)-2-{[(3,5-dichlorobenzyl)(isobutyl)amino]methyl}pyrrolidine-1-carboxylate
871499-97-7

tert-butyl (2S)-2-{[(3,5-dichlorobenzyl)(isobutyl)amino]methyl}pyrrolidine-1-carboxylate

Conditions
ConditionsYield
With sodium tris(acetoxy)borohydride In DMF (N,N-dimethyl-formamide); 1,2-dichloro-ethane for 16h;98%
4-Trifluoromethylbenzaldehyde
455-19-6

4-Trifluoromethylbenzaldehyde

4-hydroxy-3,5-diiodobenzaldehyde
1948-40-9

4-hydroxy-3,5-diiodobenzaldehyde

3,5-dibromo-4-hydroxybenzaldehyde
2973-77-5

3,5-dibromo-4-hydroxybenzaldehyde

O-phenylhydroxylamine
4846-21-3

O-phenylhydroxylamine

3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

2-Trifluoromethylbenzaldehyde
447-61-0

2-Trifluoromethylbenzaldehyde

m-formylphenyl benzoic acid
619-21-6

m-formylphenyl benzoic acid

3-Trifluoromethylbenzaldehyde
454-89-7

3-Trifluoromethylbenzaldehyde

O-(3-(trifluoromethyl)phenyl)hydroxylamine
99907-98-9

O-(3-(trifluoromethyl)phenyl)hydroxylamine

3,5-difluorobenzaldehyde
32085-88-4

3,5-difluorobenzaldehyde

2,6-dichlorobenzaldehyde
83-38-5

2,6-dichlorobenzaldehyde

benzaldehyde
100-52-7

benzaldehyde

4-Carboxybenzaldehyde
619-66-9

4-Carboxybenzaldehyde

O-(2-trifluoromethylphenyl)hydroxylamine
160725-42-8

O-(2-trifluoromethylphenyl)hydroxylamine

o-carboxybenzaldehyde
119-67-5

o-carboxybenzaldehyde

O-(3,5-difluorophenyl)hydroxylamine
197588-25-3

O-(3,5-difluorophenyl)hydroxylamine

O-(3,5-dichlorophenyl)hydroxylamine
99907-90-1

O-(3,5-dichlorophenyl)hydroxylamine

A

E-O-phenylbenzaldoxime
75735-31-8

E-O-phenylbenzaldoxime

B

3-(phenoxyimino-methyl)-benzoic acid

3-(phenoxyimino-methyl)-benzoic acid

C

2-(phenoxyimino-methyl)-benzoic acid

2-(phenoxyimino-methyl)-benzoic acid

D

4-(phenoxyimino-methyl)-benzoic acid

4-(phenoxyimino-methyl)-benzoic acid

E

3,5-dibromo-4-hydroxy-benzaldehyde O-phenyl-oxime

3,5-dibromo-4-hydroxy-benzaldehyde O-phenyl-oxime

F

3,5-difluoro-benzaldehyde O-(3,5-difluoro-phenyl)-oxime

3,5-difluoro-benzaldehyde O-(3,5-difluoro-phenyl)-oxime

G

3,5-dichloro-benzaldehyde O-(3,5-difluoro-phenyl)-oxime

3,5-dichloro-benzaldehyde O-(3,5-difluoro-phenyl)-oxime

H

4-[(3,5-dichloro-phenoxyimino)-methyl]-benzoic acid

4-[(3,5-dichloro-phenoxyimino)-methyl]-benzoic acid

I

3-[(3,5-dichloro-phenoxyimino)-methyl]-benzoic acid

3-[(3,5-dichloro-phenoxyimino)-methyl]-benzoic acid

J

2-trifluoromethyl-benzaldehyde O-(3,5-dichloro-phenyl)-oxime

2-trifluoromethyl-benzaldehyde O-(3,5-dichloro-phenyl)-oxime

K

3-trifluoromethyl-benzaldehyde O-(3,5-dichloro-phenyl)-oxime

3-trifluoromethyl-benzaldehyde O-(3,5-dichloro-phenyl)-oxime

L

3-[(3-trifluoromethyl-phenoxyimino)-methyl]-benzoic acid

3-[(3-trifluoromethyl-phenoxyimino)-methyl]-benzoic acid

M

3-trifluoromethyl-benzaldehyde O-(3,5-difluoro-phenyl)-oxime

3-trifluoromethyl-benzaldehyde O-(3,5-difluoro-phenyl)-oxime

N

2-trifluoromethyl-benzaldehyde O-(3,5-difluoro-phenyl)-oxime

2-trifluoromethyl-benzaldehyde O-(3,5-difluoro-phenyl)-oxime

O

4-trifluoromethyl-benzaldehyde O-(3,5-difluoro-phenyl)-oxime

4-trifluoromethyl-benzaldehyde O-(3,5-difluoro-phenyl)-oxime

P

4-[(3-trifluoromethyl-phenoxyimino)-methyl]-benzoic acid

4-[(3-trifluoromethyl-phenoxyimino)-methyl]-benzoic acid

Q

3-[(2-trifluoromethyl-phenoxyimino)-methyl]-benzoic acid

3-[(2-trifluoromethyl-phenoxyimino)-methyl]-benzoic acid

R

4-trifluoromethyl-benzaldehyde O-(2-trifluoromethyl-phenyl)-oxime

4-trifluoromethyl-benzaldehyde O-(2-trifluoromethyl-phenyl)-oxime

S

3-trifluoromethyl-benzaldehyde O-(2-trifluoromethyl-phenyl)-oxime

3-trifluoromethyl-benzaldehyde O-(2-trifluoromethyl-phenyl)-oxime

T

2-trifluoromethyl-benzaldehyde O-(2-trifluoromethyl-phenyl)-oxime

2-trifluoromethyl-benzaldehyde O-(2-trifluoromethyl-phenyl)-oxime

U

2-[(2-trifluoromethyl-phenoxyimino)-methyl]-benzoic acid

2-[(2-trifluoromethyl-phenoxyimino)-methyl]-benzoic acid

V

3,5-dibromo-4-hydroxy-benzaldehyde O-(3,5-dichloro-phenyl)-oxime

3,5-dibromo-4-hydroxy-benzaldehyde O-(3,5-dichloro-phenyl)-oxime

W

2-trifluoromethyl-benzaldehyde O-(3-trifluoromethyl-phenyl)-oxime

2-trifluoromethyl-benzaldehyde O-(3-trifluoromethyl-phenyl)-oxime

X

3,5-dibromo-4-hydroxy-benzaldehyde O-(3-trifluoromethyl-phenyl)-oxime

3,5-dibromo-4-hydroxy-benzaldehyde O-(3-trifluoromethyl-phenyl)-oxime

Y

4-hydroxy-3,5-diiodo-benzaldehyde O-(3-trifluoromethyl-phenyl)-oxime

4-hydroxy-3,5-diiodo-benzaldehyde O-(3-trifluoromethyl-phenyl)-oxime

Conditions
ConditionsYield
With acetic acid In water; dimethyl sulfoxide at 20℃; for 24h; Combinatorial reaction / High throughput screening (HTS);A 98%
B 98%
C 98%
D 98%
E 98%
F 98%
G 98%
H 98%
I 98%
J 98%
K 98%
L 98%
M 98%
N 98%
O 98%
P 98%
Q 98%
R 98%
S 98%
T 98%
U 98%
V 98%
W 98%
X 98%
Y 98%
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

8-bromo-5,6-dihydro-4H-benzo[f][1,2,3]triazolo[1,5-a][1,4]diazepine
1266452-21-4

8-bromo-5,6-dihydro-4H-benzo[f][1,2,3]triazolo[1,5-a][1,4]diazepine

C17H13BrCl2N4
1358787-29-7

C17H13BrCl2N4

Conditions
ConditionsYield
With sodium tris(acetoxy)borohydride; acetic acid In 1,2-dichloro-ethane98%
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

3,5-dichlorobenzaldehyde oxime

3,5-dichlorobenzaldehyde oxime

Conditions
ConditionsYield
With hydroxylamine hydrochloride; sodium acetate In ethanol; dichloromethane; water98%
5-hydroxy-2,3-dihydro-1H-indene-1-one
3470-49-3

5-hydroxy-2,3-dihydro-1H-indene-1-one

3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

(E)-2-(3,5-dichlorobenzylidene)-5-hydroxy-2,3-dihydro-1H-inden-1-one

(E)-2-(3,5-dichlorobenzylidene)-5-hydroxy-2,3-dihydro-1H-inden-1-one

Conditions
ConditionsYield
With sodium hydroxide In methanol at 20℃;98%
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

ethylenediamine
107-15-3

ethylenediamine

N,N'-(ethane-1,2-diyl)bis(1-(3,5-dichlorophenyl)methanimine)

N,N'-(ethane-1,2-diyl)bis(1-(3,5-dichlorophenyl)methanimine)

Conditions
ConditionsYield
In ethanol at 20℃; for 6h;96%
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

cyclohexylamine
108-91-8

cyclohexylamine

cychlohexyl(3,5-dichlorobenzyl)amine

cychlohexyl(3,5-dichlorobenzyl)amine

Conditions
ConditionsYield
Stage #1: 3,5-dichlorobenzaldehyde; cyclohexylamine In methanol at 20℃; for 1h;
Stage #2: With sodium tetrahydroborate In methanol at 20℃;
95.4%
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

ethyl acetoacetate
141-97-9

ethyl acetoacetate

diethyl 4-(3,5-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate
897627-79-1

diethyl 4-(3,5-dichlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate

Conditions
ConditionsYield
With ammonium acetate; phenylboronic acid In ethanol for 4h; Hantzsch reaction; Heating;95%
With cadmium(II) nitrate tetrhydrate; ammonium acetate In neat (no solvent) at 80℃; for 3h; Hantzsch Dihydropyridine Synthesis; Green chemistry;89%
With ammonium acetate; triphenylphosphine In ethanol for 4h; Hantzsch reaction; Reflux;80%
With ammonium acetate; triethylamine at 80℃; for 2h; Hantzsch condensation; Neat (no solvent);52%
With ammonia In ethanol; water at 20 - 95℃; for 4h;28%
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

3,4,5-trimethoxybenzohydrazide
3291-03-0

3,4,5-trimethoxybenzohydrazide

C17H16Cl2N2O4

C17H16Cl2N2O4

Conditions
ConditionsYield
In ethanol for 0.5h; Heating;94.7%
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

methyl 2-naphthyl ketone
93-08-3

methyl 2-naphthyl ketone

(2E)-1-(2-naphthyl)-3-(3,5-dichlorophenyl)-2-propen-1-one
1352444-94-0

(2E)-1-(2-naphthyl)-3-(3,5-dichlorophenyl)-2-propen-1-one

Conditions
ConditionsYield
With potassium hydroxide In methanol; water at 20℃; for 24h; Aldol condensation;94%
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

anthranilic acid amide
28144-70-9

anthranilic acid amide

2,3-dihydro-2-(2,4-dichlorophenyl)quinazolin-4(1H)-one
359430-31-2

2,3-dihydro-2-(2,4-dichlorophenyl)quinazolin-4(1H)-one

Conditions
ConditionsYield
With antimony(III) chloride In methanol at 20℃; for 0.233333h;94%
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

1-(4-chlorophenyl)-2-(1H-imidazol-1-yl)ethan-1-one
24155-32-6

1-(4-chlorophenyl)-2-(1H-imidazol-1-yl)ethan-1-one

(E)-1-(4-Chloro-phenyl)-3-(3,5-dichloro-phenyl)-2-imidazol-1-yl-propenone

(E)-1-(4-Chloro-phenyl)-3-(3,5-dichloro-phenyl)-2-imidazol-1-yl-propenone

Conditions
ConditionsYield
With piperidine; acetic acid In benzene Heating;93%
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

phenylacetylene
536-74-3

phenylacetylene

(-)-(1S)-1-(3,5-dichlorophenyl)-3-phenylprop-2-yn-1-ol

(-)-(1S)-1-(3,5-dichlorophenyl)-3-phenylprop-2-yn-1-ol

Conditions
ConditionsYield
Stage #1: phenylacetylene With (-)-N-methylephedrine; triethylamine; zinc trifluoromethanesulfonate In toluene for 0.25h;
Stage #2: 3,5-dichlorobenzaldehyde In toluene Further stages.;
93%
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

4-hydroxy 2,6-dimethylpyrimidine
6622-92-0

4-hydroxy 2,6-dimethylpyrimidine

2-[2-(3,5-dichloro-phenyl)-vinyl]-6-methyl-pyrimidin-4-ol

2-[2-(3,5-dichloro-phenyl)-vinyl]-6-methyl-pyrimidin-4-ol

Conditions
ConditionsYield
In acetic anhydride93%
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

1,1-dimethylhydrazine
57-14-7

1,1-dimethylhydrazine

3,5-dichlorobenzaldehyde N,N-dimethylhydrazone
1362849-52-2

3,5-dichlorobenzaldehyde N,N-dimethylhydrazone

Conditions
ConditionsYield
With magnesium sulfate In dichloromethane at 20℃; Inert atmosphere;93%
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

(trimethylsilyl)methylmagnesium chloride
13170-43-9

(trimethylsilyl)methylmagnesium chloride

1-(3,5-dichlorophenyl)-2-(trimethylsilyl)ethanol
136272-29-2

1-(3,5-dichlorophenyl)-2-(trimethylsilyl)ethanol

Conditions
ConditionsYield
In diethyl ether Ambient temperature;92%
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

phenylacetylene
536-74-3

phenylacetylene

(+)-(1R)-1-(3,5-dichlorophenyl)-3-phenylprop-2-yn-1-ol

(+)-(1R)-1-(3,5-dichlorophenyl)-3-phenylprop-2-yn-1-ol

Conditions
ConditionsYield
Stage #1: phenylacetylene With triethylamine; zinc trifluoromethanesulfonate In toluene for 0.25h;
Stage #2: 3,5-dichlorobenzaldehyde In toluene Further stages.;
92%
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

benzil
134-81-6

benzil

2-(3,5-dichlorophenyl)-4,5-diphenyl-1H-imidazole
1259065-14-9

2-(3,5-dichlorophenyl)-4,5-diphenyl-1H-imidazole

Conditions
ConditionsYield
With iron(III) phosphate; ammonium acetate In ethanol for 4h; Reflux;92%
3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

1,2-diamino-benzene
95-54-5

1,2-diamino-benzene

1-(3,5-dichlorobenzyl)-2-(3,5-dichlorophenyl)-1H-1,3-benzimidazole
1370018-48-6

1-(3,5-dichlorobenzyl)-2-(3,5-dichlorophenyl)-1H-1,3-benzimidazole

Conditions
ConditionsYield
With iron(III) phosphate at 20℃; for 0.666667h; Neat (no solvent);92%
methyl (3,4,5-trimethoxyphenyl) ketone
1136-86-3

methyl (3,4,5-trimethoxyphenyl) ketone

3,5-dichlorobenzaldehyde
10203-08-4

3,5-dichlorobenzaldehyde

(2E)-1-(3',4',5'-trimethoxyphenyl)-3-(3,5-dichlorophenyl)-2-propen-1-one
1442690-93-8

(2E)-1-(3',4',5'-trimethoxyphenyl)-3-(3,5-dichlorophenyl)-2-propen-1-one

Conditions
ConditionsYield
With potassium hydroxide In methanol at 20℃; for 24h; Aldol Condensation;92%

3,5-Dichlorobenzaldehyde Chemical Properties

Molecular structure of Benzaldehyde, 3,5-dichloro- (CAS NO.10203-08-4) is:

Product Name: Benzaldehyde, 3,5-dichloro-
CAS Registry Number: 10203-08-4
IUPAC Name: 3,5-Dichlorobenzaldehyde
Molecular Weight: 175.01206 [g/mol]
Molecular Formula: C7H4Cl2O
XLogP3-AA: 2.6
H-Bond Donor: 0
H-Bond Acceptor: 1 
EINECS: 233-499-0
Melting Point: 63.5-65.5 °C(lit.)
Surface Tension: 45.1 dyne/cm
Density: 1.4 g/cm3
Flash Point: 98.3 °C
Enthalpy of Vaporization: 47.81 kJ/mol
Boiling Point: 241.1 °C at 760 mmHg
Vapour Pressure: 0.0365 mmHg at 25°C
Product Categories: Aromatic Aldehydes & Derivatives (substituted);Benzaldehyde;Aldehydes;C7;Carbonyl Compounds

3,5-Dichlorobenzaldehyde Safety Profile

Safty information about Benzaldehyde, 3,5-dichloro- (CAS NO.10203-08-4) is:
Hazard Codes: CorrosiveC; IrritantXi,Xn
Risk Statements: 34-36/37/38-22
34:  Causes burns 
36/37/38:  Irritating to eyes, respiratory system and skin 
22:  Harmful if swallowed  
Safety Statements: 26-36/37/39-45-22-37/39
26:  In case of contact with eyes, rinse immediately with plenty of water and seek medical advice 
36/37/39:  Wear suitable protective clothing, gloves and eye/face protection 
45:  In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) 
22:  Do not breathe dust 
37/39:  Wear suitable gloves and eye/face protection   
RIDADR: UN 3261 8/PG 2
WGK Germany: 3
F: 10: Keep under argon.
Hazard Note: Corrosive
HazardClass: 8
PackingGroup: III
HS Code: 29130000

3,5-Dichlorobenzaldehyde Specification

 Benzaldehyde, 3,5-dichloro- , its cas register number is 10203-08-4. It also can be called NSC 109095 ; 3,5-Dichlorobenzaldehyde . It is a white to slightly yellow fluffy powder.

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