2,6-Dichlorobenzaldehyde supplier

Name
2,6-Dichlorobenzaldehyde
EINECS 201-472-2
CAS No. 83-38-5
Article Data111
CAS DataBase
Density 1.4 g/cm³
Solubility <0.1 g/100 mL at 23 °C in water
Melting Point 69-71 °C(lit.)
Formula C₇H₄Cl₂O
Boiling Point 239.2 °C at 760 mmHg
Molecular Weight 175.014
Flash Point 97.4 °C
Transport Information UN 3261 8/PG 2
Appearance white to light yellow powder
Safety 26-27-28-36/37/39-45-37/39
Risk Codes 34-36/37/38
Molecular Structure
Hazard Symbols C, Xi
Synonyms 2,6-Dichlorobenzaldehyde
PSA 17.07000
LogP 2.80590

Synthetic route

: 15258-73-8
2,6-dichlorobenzyl alcohol

: 83-38-5
2,6-dichlorobenzaldehyde

Conditions

Conditions	Yield
With dmap; tetrakis(actonitrile)copper(I) hexafluorophosphate; N,N'-di-tert-butylethylenediamine; oxygen In dichloromethane at 20℃; under 760.051 Torr; for 3h; Schlenk technique; Molecular sieve; Sealed tube;	99%
With tert.-butylnitrite; oxygen; acetic acid In toluene at 50℃; for 8.5h;	99%
With 2,2'-azobis(isobutyronitrile); oxygen; sodium bromide In 1,4-dioxane at 70℃;	94%

: 2828-47-9
2,6-Dichlorobenzaldehyde N,N-dimethylhydrazone

: 83-38-5
2,6-dichlorobenzaldehyde

Conditions

Conditions	Yield
With 3-benzyl-5-(2-hydroxyethyl)-4-methyl-1,3-thiazol-3-ium chloride In chloroform at 20℃; for 1h; oxidative cleavage;	98%
With chloro-trimethyl-silane; sodium iodide In water; acetonitrile for 0.0333333h; deprotection;	94%
With triethylene diamine nickel thiosulfate; water In chloroform at 20℃; for 0.166667h; Hydrolysis;	94%
With iron(II) sulfate In chloroform at 20℃; for 0.75h; Hydrolysis;	88%

: 25185-95-9
2,6-dichlorobenzaldoxime

: 83-38-5
2,6-dichlorobenzaldehyde

Conditions

Conditions	Yield
With Cr-MCM-41 zeolite on silica gel for 0.1h; microwave irradiation;	98%
With 2,6-dicarboxypyridinium fluorochromate for 0.5h;	96%
With potassium permanganate; 1-n-butyl-3-methylimidazolim bromide at 20℃; for 0.383333h; Ionic liquid; chemoselective reaction;	91%

: 89-98-5
2-chloro-benzaldehyde

: 83-38-5
2,6-dichlorobenzaldehyde

Conditions

Conditions	Yield
With N-chloro-succinimide; palladium diacetate; silver trifluoroacetate; anthranilic acid; trifluoroacetic acid In 1,2-dichloro-ethane at 60℃; for 24h; Sealed tube;	95%
With N-chloro-succinimide; 2-hydroxyl-5-nitro-3-(trifluoromethyl)pyridine; 4-trifluoromethylphenylamine; palladium diacetate; trifluoroacetic acid In 1,2-dichloro-ethane at 80℃; for 24h; Sealed tube;	92%

: 2014-83-7
1,3-Dichloro-2-chloromethyl-benzene

: 83-38-5
2,6-dichlorobenzaldehyde

Conditions

Conditions	Yield
With dihydrogen peroxide; trimethylamine In water for 2h; Reflux;	94%

: 2-(2,6-dichlorophenyl)-1,3-dithiane

: 83-38-5
2,6-dichlorobenzaldehyde

Conditions

Conditions	Yield
With 1,3,5-trichloro-2,4,6-triazine; dimethyl sulfoxide In dichloromethane at 20℃; for 2.15h;	91%

: 51379-82-9
2,6-Dichlorbenzaldehyd-2,4-dinitrophenylhydrazon

: 83-38-5
2,6-dichlorobenzaldehyde

Conditions

Conditions	Yield
With potassium permanganate at 40℃; for 2.8h; Ionic liquid; chemoselective reaction;	81%

: 2,6-dichlorobenzaldehyde dimethyl acetal

: 83-38-5
2,6-dichlorobenzaldehyde

Conditions

Conditions	Yield
With β‐cyclodextrin In methanol; water at 50℃; for 10h;	80%

: 33486-90-7
1,3-dichloro-2-methoxymethylbenzene

: 83-38-5
2,6-dichlorobenzaldehyde

Conditions

Conditions	Yield
With N-Bromosuccinimide In tetrachloromethane for 1h; Irradiation; Reflux;	77%

: 82073-58-3
2-(2,6-dichlorophenyl)-1,3-dioxolane

: 6399-81-1
triphenylphosphine hydrobromide

A: 83-38-5
2,6-dichlorobenzaldehyde

B: 7237-34-5
2-(hydroxyethyl)triphenylphosphonium bromide

Conditions

Conditions	Yield
In dichloromethane at 50℃; for 0.0833333h; Microwave irradiation; Sealed tube;	A 76% B n/a

...Expand

: 32188-71-9
2,6-dichlorobenzaldehyde (2,6-dichlorobenzylidene)hydrazone

: 83-38-5
2,6-dichlorobenzaldehyde

Conditions

Conditions	Yield
With ammonium cerium(IV) nitrate In water; acetonitrile at 50℃; for 15h; Oxidation;	57%

: 74105-85-4
d,l-1,2-Bis(2,6-dichlorphenyl)-N,N'-diethylethylendiamin

A: 83-38-5
2,6-dichlorobenzaldehyde

B: 74105-78-5
4-Chlor-2-(2,6-dichlorphenyl)-1-ethylindol

C: 74105-79-6
4,9-Dichlor-5,10-diethyl-4b,5,9b,10-tetrahydroindolo<3,2-b>indol

Conditions

Conditions	Yield
at 215℃; for 0.25h;	A 4% B 53% C 22%

...Expand

: 104669-26-3, 33629-92-4
(2,6-dichlorobenzylidene)aniline

: 83-38-5
2,6-dichlorobenzaldehyde

Conditions

Conditions	Yield
With hydrogenchloride; water In diethyl ether; toluene at 20℃; for 2h; Inert atmosphere;	32%

: 10345-78-5
2,6-dichloro-N,N-diethylbenzamide

: 83-38-5
2,6-dichlorobenzaldehyde

Conditions

Conditions	Yield
With Schwartz's reagent In tetrahydrofuran at 20℃; for 18h;	17%

: 2,6-dichlorobenzyl azide

: 83-38-5
2,6-dichlorobenzaldehyde

Conditions

Conditions	Yield
With sodium dithionite; spermwhale myoglobin (H64V,V68A) In methanol; aq. phosphate buffer at 20℃; for 24h; pH=7; Catalytic behavior;	1%
With sodium dithionite In methanol; aq. phosphate buffer at 20℃; for 24h; pH=7; Catalytic behavior; Enzymatic reaction;

: 115231-29-3
2,6-dichloro-benzaldehyde-[N-(4-dimethylamino-phenyl)-oxime ]

: 83-38-5
2,6-dichlorobenzaldehyde

Conditions

Conditions	Yield
With sulfuric acid

: 81-19-6
2,6-dichlorobenzalchloride

: 83-38-5
2,6-dichlorobenzaldehyde

Conditions

Conditions	Yield
With sulfuric acid anschliessenden Behandeln mit Eis;
With ethanol; silver nitrate

: 60329-03-5
guanabenz

A: 83-38-5
2,6-dichlorobenzaldehyde

B: 79-17-4
aminoguanidine

Conditions

Conditions	Yield
With hydrogenchloride In water at 37℃; for 10h; effect of pH on the reversibility;

: C16H10Cl4O3

: 83-38-5
2,6-dichlorobenzaldehyde

Conditions

Conditions	Yield
Yield given. Multistep reaction;

: 68-12-2, 33513-42-7
N,N-dimethyl-formamide

: 541-73-1
1,3-Dichlorobenzene

: 83-38-5
2,6-dichlorobenzaldehyde

Conditions

Conditions	Yield
With n-butyllithium 1.) hexane,THF, -65 to -70 deg C, 45 min, 2.) THF, -70 deg C, 45 min; Yield given. Multistep reaction;
Stage #1: 1,3-Dichlorobenzene With n-butyllithium; N,N,N,N,-tetramethylethylenediamine; diisopropylamine In tetrahydrofuran at -78℃; for 1h; Inert atmosphere; Stage #2: N,N-dimethyl-formamide at -78℃; for 0.5h; Inert atmosphere; regioselective reaction;
Stage #1: 1,3-Dichlorobenzene With lithium diisopropyl amide In 1,2-dimethoxyethane; n-heptane; ethylbenzene at -60℃; for 1h; Stage #2: N,N-dimethyl-formamide In 1,2-dimethoxyethane; n-heptane; ethylbenzene at -60℃; for 0.5h; Cooling with ice;

: 112792-78-6
1,2-di-(2,6-dichlorophenyl)-1,2-ethanediol

: 83-38-5
2,6-dichlorobenzaldehyde

Conditions

Conditions	Yield
With 1-Benzyl-1,4-dihydronicotinamide; oxygen; meso-tetraphenylporphyrin iron(III) chloride In dichloromethane for 12h; Ambient temperature; Irradiation;	20 % Chromat.

: 83-38-5
2,6-dichlorobenzaldehyde

: 25185-95-9
2,6-dichlorobenzaldoxime

Conditions

Conditions	Yield
With hydroxylamine hydrochloride	100%
With pyridine; hydroxylamine hydrochloride at 20℃; for 0.166667h;	100%
With pyridine; hydroxylamine hydrochloride at 20℃; for 0.166667h;	100%

: 83-38-5
2,6-dichlorobenzaldehyde

: 6575-28-6
(1E)-2,6-dichlorobenzaldehyde oxime

Conditions

Conditions	Yield
With pyridine; hydroxylamine hydrochloride In ethanol	100%
With hydroxylamine hydrochloride; sodium hydroxide In ethanol; water at 80 - 90℃; for 18 - 24h;	96%
With hydroxylamine hydrochloride; sodium hydroxide In ethanol; water at 90℃; for 24h;	96%

: 108-94-1
cyclohexanone

: 83-38-5
2,6-dichlorobenzaldehyde

: (2S,1'R)-2-[(2,6-dichlorophenyl)hydroxymethyl]cyclohexan-1-one

Conditions

Conditions	Yield
With C18H17F6N5; 2,4-dinitrobenzoic acid In neat (no solvent) at 0℃; for 48h; Aldol Addition;	100%
With C35H55N3O5; water at -20℃; for 24h; Aldol Condensation; enantioselective reaction;	99%
trans-4-hydroxy-L-prolinamide derivative In water at 25℃; for 5h;	95%

: 141-97-9
ethyl acetoacetate

: 83-38-5
2,6-dichlorobenzaldehyde

: 371981-20-3
2-(2,6-dichlorophenyl)-4-hydroxy-4-methyl-6-oxo-cyclohexane-1,3-dicarboxylic acid diethyl ester

Conditions

Conditions	Yield
With piperidine In ethanol at 20℃;	100%
With piperidine In ethanol Inert atmosphere;	68%

: 2579-20-6
cis, trans-1,3-dimethylaminocyclohexane

: 83-38-5
2,6-dichlorobenzaldehyde

: 1217526-98-1
C22H22Cl4N2

Conditions

Conditions	Yield
In methanol at 20℃; Molecular sieve;	100%
In methanol at 20℃; Molecular sieve;

: 769-42-6
1,3-dimethylbarbituric acid

: 83-38-5
2,6-dichlorobenzaldehyde

: 126-81-8
dimedone

: 109-89-7
diethylamine

: C21H22Cl2N2O5*C4H11N

Conditions

Conditions	Yield
In water at 20℃; Inert atmosphere;	100%

...Expand

: 83-38-5
2,6-dichlorobenzaldehyde

: 126-81-8
dimedone

: 109-89-7
diethylamine

: Diethylammonium 2-((2,6-dichlorophenyl)(2-hydroxy-4,4-dimethyl-6-oxocyclohex-1-en-1-yl)methyl)-5,5-dimethyl-3-oxocyclohex-1-enolate

Conditions

Conditions	Yield
In water at 20℃; Inert atmosphere;	100%

...Expand

: 83-38-5
2,6-dichlorobenzaldehyde

: 75-08-1
ethanethiol

: 1186033-44-2
C9H9ClOS

Conditions

Conditions	Yield
Stage #1: ethanethiol With sodium hydroxide In water at 20℃; for 0.5h; Stage #2: 2,6-dichlorobenzaldehyde With tetrabutylammomium bromide In water at 82℃;	99.4%
Stage #1: ethanethiol With sodium hydroxide In water for 1h; Stage #2: 2,6-dichlorobenzaldehyde With tetrabutylammomium bromide In water for 4h; Reflux;

: 83-38-5
2,6-dichlorobenzaldehyde

: 109-77-3
malononitrile

: 2972-79-4
2-(2,6-dichlorobenzylidene)malononitrile

Conditions

Conditions	Yield
In water at 20℃; for 0.166667h; Knoevenagel Condensation; Green chemistry;	99%
With ZnO/Al-SBA-15 (40) In ethanol at 20℃; for 2h; Knoevenagel Condensation; Green chemistry;	97%
With zirconium(IV) oxide In ethanol for 2h; Knoevenagel Condensation; Reflux;	95%

: 83-38-5
2,6-dichlorobenzaldehyde

: 15258-73-8
2,6-dichlorobenzyl alcohol

Conditions

Conditions	Yield
With sodium tetrahydroborate In methanol at 0℃;	99%
With sodium tetrahydroborate In ethanol at 20℃; for 2h;	94%
With Triethoxysilane; C27H42FeP4S In tetrahydrofuran at 50℃; for 2h; Catalytic behavior; Schlenk technique; Green chemistry;	93%

: 83-38-5
2,6-dichlorobenzaldehyde

4-acetylbenzenesulfonyl-Rink resin: 4-acetylbenzenesulfonyl-Rink resin

: 4-[(2E)-3-(2,6-dichlorophenyl)prop-2-enoyl]benzenesulfonamide

Conditions

Conditions	Yield
Stage #1: 2,6-dichlorobenzaldehyde; 4-acetylbenzenesulfonyl-Rink resin With sodium ethanolate In tetrahydrofuran; ethanol at 20℃; for 0.5h; Stage #2: With trifluoroacetic acid In dichloromethane Further stages.;	99%

: 83-38-5
2,6-dichlorobenzaldehyde

: 109-76-2
Trimethylenediamine

: 348630-62-6
N,N'-bis(2,6-dichlorobenzylidene)propane-1,3-diamine

Conditions

Conditions	Yield
In ethanol for 0.5h; Heating;	99%
In benzene for 24h; Heating;	72.07%

: 83-38-5
2,6-dichlorobenzaldehyde

: 2,4,5-tris(2,6-dichlorophenyl)-4,5-dihydro-1H-imidazole

Conditions

Conditions	Yield
With ammonium chloride In ethanol at 20℃; for 192h;	99%

: 686746-12-3
3-chloro-1,1-dimethylpropylamine hydrochloride

: 83-38-5
2,6-dichlorobenzaldehyde

: 686746-13-4
(3-chloro-1,1-dimethylpropyl)-(2,6-dichlorobenzylidene)-amine

Conditions

Conditions	Yield
Stage #1: 3-chloro-1,1-dimethylpropylamine-hydrochloride With sodium hydroxide In water at 0℃; for 0.5h; Stage #2: 2,6-dichlorobenzaldehyde In dichloromethane at 20℃; for 18h;	99%

: 83-38-5
2,6-dichlorobenzaldehyde

: 762-72-1
allyl-trimethyl-silane

: 1200328-43-3
1,3-dichloro-2-[1-[(trimethylsilyl)oxy]-3-buten-1-yl]benzene

Conditions

Conditions	Yield
With Montmorillonite K10 clay In dichloromethane at 0 - 20℃; for 1.08333h; Hosomi-Sakurai reaction;	99%
With C76H92CoN4(1+)*F6Sb(1-) In 1,2-dichloro-ethane at 100℃; for 4h; Sealed tube;

: 108-94-1
cyclohexanone

: 83-38-5
2,6-dichlorobenzaldehyde

: 2-[hydroxy-(2,6-dichlorophenyl)-methyl]-cyclohexan-1-one

Conditions

Conditions	Yield
With (S)-N-( p-dodecylphenylsulfonyl)-2-pyrrolidinecarboxamide; water In 1,2-dichloro-ethane at 20℃; for 48h; Aldol condensation; optical yield given as %ee; enantioselective reaction;	99%

: 161149-23-1
3-(dimethylcarbamothioyl)-1-methyl-1H-imidazol-3-ium chloride

: 83-38-5
2,6-dichlorobenzaldehyde

: 1413413-86-1
O-(2,6-dichlorophenyl)(1-methyl-1H-imidazol-2-yl)methyl dimethylcarbamothioate

Conditions

Conditions	Yield
With triethylamine In N,N-dimethyl-formamide at 30℃; for 12h; Temperature; Inert atmosphere;	99%

: (4R,5R)-4-benzyloxycarbonylamino-5-isopropylpyrazolidin-3-one

: 83-38-5
2,6-dichlorobenzaldehyde

: (3R,4R,Z)-4-(benzyloxycarbonylamino)-2-(2,6-dichlorobenzylidene)-3-isopropyl-5-oxopyrazolidin-2-ium-1-ide

Conditions

Conditions	Yield
Stage #1: (4R,5R)-4-benzyloxycarbonylamino-5-isopropylpyrazolidin-3-one; 2,6-dichlorobenzaldehyde In methanol at 20℃; for 0.0833333h; Stage #2: With trifluoroacetic acid In methanol at 20℃; for 7h;	99%

: 766-82-5
1-ethynyl-3-methyl-benzene

: 83-38-5
2,6-dichlorobenzaldehyde

: 1590443-25-6
C16H12Cl2O

Conditions

Conditions	Yield
With 2,2,2-Trifluoroacetophenone; triphenylphosphine In water at 60℃; for 2h; Schlenk technique; Inert atmosphere; Green chemistry;	99%

: 4-benzyloxycarbonylamino-5-isopropyl-3-pyrazolidinone

: 83-38-5
2,6-dichlorobenzaldehyde

: (3R,4R,Z)-4-(benzyloxycarbonylamino)-2-(2,6-dichlorobenzylidene)-3-isopropyl-5-oxopyrazolidin-2-ium-1-ide

Conditions

Conditions	Yield
With trifluoroacetic acid In methanol	99%

: 67-56-1
methanol

: 83-38-5
2,6-dichlorobenzaldehyde

: 2,6-dichlorobenzaldehyde dimethyl acetal

Conditions

Conditions	Yield
With Eosin Y In acetonitrile at 20℃; for 12h; Schlenk technique; Inert atmosphere; Irradiation; chemoselective reaction;	99%
With titanium tetrachloride; triethylamine In dichloromethane at 0 - 20℃; for 0.5h; Inert atmosphere;	93%

: 83-38-5
2,6-dichlorobenzaldehyde

: 25015-63-8
4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane

: 2-((2,6-dichlorobenzyl)oxy)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Conditions

Conditions	Yield
With C34H28N6Zn In neat (no solvent) at 20℃; for 2h; Glovebox; Schlenk technique;	99%
With C24H34N5PSeTi In toluene at 30℃; for 3h; Glovebox; Schlenk technique; chemoselective reaction;	93%
With C45H69FeN8PSi2 In tetrahydrofuran at 20℃; for 6h; Inert atmosphere; Schlenk technique;

: 108-24-7
acetic anhydride

: 83-38-5
2,6-dichlorobenzaldehyde

: 24653-82-5
1,1-diacetoxy-1-(2,6-dichlorophenyl)methane

Conditions

Conditions	Yield
With p-toluenesulfonic acid-paraformaldehyde copolymer at 25℃; for 0.25h; Neat (no solvent);	98%
aluminium dodecatungsten phosphate at 20℃; for 0.25h;	95%
With lithium trifluoromethanesulfonate at 20℃; for 19h;	95%

: 83-38-5
2,6-dichlorobenzaldehyde

: 1194-65-6
2,6-dichloro-benzonitrile

Conditions

Conditions	Yield
With aluminum oxide; hydroxylamine hydrochloride; methanesulfonyl chloride at 100℃; for 0.333333h;	98%
With ammonia; oxygen In tert-Amyl alcohol at 40℃; under 750.075 Torr; for 24h; Green chemistry;	94%
With manganese(IV) oxide; ammonia; magnesium sulfate In tetrahydrofuran; isopropyl alcohol at 20℃; for 17h;	93%

: 83-38-5
2,6-dichlorobenzaldehyde

: 80474-99-3
tetraethyl (aminomethylene)bis(phosphonate)

: [{[1-(2,6-Dichloro-phenyl)-meth-(E)-ylidene]-amino}-(diethoxy-phosphoryl)-methyl]-phosphonic acid diethyl ester

Conditions

Conditions	Yield
In diethyl ether for 2h;	98%

: 83-38-5
2,6-dichlorobenzaldehyde

: 3714-77-0
2,6-dichlorobenzaldoxime

Conditions

Conditions	Yield
With hydroxylamine hydrochloride; titanium(IV) oxide at 80℃; for 0.166667h;	98%
With hydroxylamine hydrochloride; sodium hydroxide In ethanol; water at 0 - 20℃; for 2h;	96%
With cadmium sulfate; hydroxylamine hydrochloride for 0.0833333h; Microwave irradiation; stereoselective reaction;	85%
With hydroxylamine hydrochloride; potassium carbonate at 90℃; for 5h;	90 % Spectr.
With aluminum oxide; methanesulfonic acid at 80℃; for 0.0833333h;	95 % Spectr.

: 83-38-5
2,6-dichlorobenzaldehyde

: 308356-30-1
2-amino-6-hydrazino-4-pyrrolidino-5-pyrimidinecarbonitrile

: 2-Amino-4-{N'-[1-(2,6-dichloro-phenyl)-meth-(E)-ylidene]-hydrazino}-6-pyrrolidin-1-yl-pyrimidine-5-carbonitrile

Conditions

Conditions	Yield
With acetic acid In ethanol for 1h; Heating;	98%

2,6-Dichlorobenzaldehyde Chemical Properties

The Molecular Structure of 2,6-Dichlorobenzaldehyde (CAS NO.83-38-5):

Empirical Formula: C₇H₄Cl₂O
Molecular Weight: 175.0121
IUPAC Name: 2,6-dichlorobenzaldehyde
Appearance: white to light yellow powder
Nominal Mass: 174 Da
Average Mass: 175.0121 Da
Monoisotopic Mass: 173.96392 Da
Index of Refraction: 1.6
Molar Refractivity: 42.79 cm³
Molar Volume: 125 cm³
Surface Tension: 45.1 dyne/cm
Density: 1.4 g/cm³
Flash Point: 97.4 °C
Enthalpy of Vaporization: 47.61 kJ/mol
Boiling Point: 239.2 °C at 760 mmHg
Vapour Pressure: 0.0406 mmHg at 25°C
Water Solubility: <0.1 g/100 mL at 23 ºC
Sensitive: Air Sensitive
Stability: Stable. Incompatible with strong oxidizing agents, strong bases. Air, light and moisture sensitive
InChI
InChI=1/C7H4Cl2O/c8-6-2-1-3-7(9)5(6)4-10/h1-4H
Smiles
c1(c(cccc1Cl)Cl)C=O
Product Categories: Benzaldehyde;Dicloxacillin;Aldehydes;C7;Carbonyl Compounds
Synonyms: CCRIS 6014 ; EINECS 201-472-2 ; Benzaldehyde, 2,6-dichloro-

2,6-Dichlorobenzaldehyde Uses

2,6-Dichlorobenzaldehyde (CAS NO.83-38-5) can be used for the synthesis of dyes, intermediates of pesticide and pharmaceuticalare, also used as fungicides and herbicides and used in the manufacture of 2,6 - dichlorobenzonitrile .

2,6-Dichlorobenzaldehyde Safety Profile

Hazard Codes: Irritant Xi Corrosive C
Risk Statements: 34-36/37/38
R34: Causes burns
R36/37/38: Irritating to eyes, respiratory system and skin
Safety Statements: 26-27-28-36/37/39-45-37/39
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
S27: Take off immediately all contaminated clothing
S28: After contact with skin, wash immediately with plenty of soap-suds
S36/37/39: Wear suitable protective clothing, gloves and eye/face protection
S45: In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible)
S37/39: Wear suitable gloves and eye/face protection
RIDADR: UN 3261 8/PG 2
WGK Germany: 2
Hazard Note: Corrosive
HazardClass: 8
PackingGroup: III
HS Code: 29130000

Product Name

2,6-Dichlorobenzaldehyde

Synthetic route

2,6-Dichlorobenzaldehyde Chemical Properties

2,6-Dichlorobenzaldehyde Uses

2,6-Dichlorobenzaldehyde Safety Profile

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