o-chlorobenzaldoxime

Suppliers

Names

[ Name ]:
o-chlorobenzaldoxime

[Synonym ]:
2-chlorobenzaldoxime
O-CHLOROBENZALDEHYDE OXIME
(Z)-2-chlorobenzaldehyde oxiMe
MFCD00016406
2-chloro benzaldehyde oxime
(E)-1-(2-Chlorophenyl)-N-hydroxymethanimine
o-chlorobenzaldoxime
(E/Z)-2-chlorobenzaldehyde oxime
N-(2-Chlorobenzylidene)hydroxylamine
2-chlorobenzaldehyde oxime
2-chlorobenzenecarbaldehyde oxime
Benzaldehyde, 2-chloro-, oxime
EINECS 223-065-9
Benzaldehyde, o-chloro-, oxime

Chemical & Physical Properties

[ Density]:
1.21g/cm3

[ Boiling Point ]:
242.6ºC at 760mmHg

[ Melting Point ]:
73-76 °C(lit.)

[ Molecular Formula ]:
C₇H₆ClNO

[ Molecular Weight ]:
155.58200

[ Flash Point ]:
100.5ºC

[ Exact Mass ]:
155.01400

[ PSA ]:
32.59000

[ LogP ]:
2.14810

[ Index of Refraction ]:
1.55

[ Water Solubility ]:
insoluble

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2928000090

Precursor & DownStream

Precursor

DownStream

(3-(2-CHLOROPHENYL)ISOXAZOL-5-YL)METHANOL
methyl 3-(2-chlorophenyl)-5-methyl-1,2-oxazole-4-carboxylate
(2-chlorophenyl)(hydroxyimino)acetonitrile
Oxazole,2-(2-chlorophenyl)-5-phenyl-
5-BROMOMETHYL-3-(2-CHLORO-PHENYL)-ISOXAZOLE
2-Chloroaniline
2-Chlorobenzaldehyde
2-CHLOROBENZAMIDEOXIME
2-chlorophenyl isothiocyanate
2-Chlorobenzonitrile

Customs

[ HS Code ]: 2928000090

[ Summary ]:
2928000090 other organic derivatives of hydrazine or of hydroxylamine VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

Articles

A mild and selective method for the conversion of oximes into ketones and aldehydes by the use of N-bromophthalimide. Khazaei A, et al.

J. Chem. Res. (M) 2004(10) , 695-696, (2004)

Solid-phase synthesis of 5-isoxazol-4-yl-[1,2,4] oxadiazoles. Quan C and Kurth M.

J. Org. Chem. 69(5) , 1470-1474, (2004)

Amberlyst 15 supported nitrosonium ion as an efficient reagent for regeneration of carbonyl compounds from oximes, hydrazones and semicarbazones. Lakouraj MM, et al.

Reactive funct. Polym. 66(9) , 910-915, (2006)

o-Chlorobenzaldoxime
O-phenyl-4-chlorobenzaldoxime
o-(3-Amino-4-sodiooxybenzoyl)benzoic acid sodium salt
O-(OCTYLPHOSPHORYL)CHOLINE SOLUTION
o-Nitrobenzyl-5 tetrahydro-5,6,7,7a 4H-thieno(3,2-c)pyridinone-2 oxala te [French]
O-Desmethyl apixaban
3-[(2-Hydroxypropyl)(methyl)amino]-4-methylcyclohexan-1-one
3-(4-Methyl-1,4-diazepan-1-yl)-4-propylcyclohexan-1-ol
3-[Cyclopropyl(2-methoxyethyl)amino]-4-propylcyclohexan-1-ol
3-[(4-Methoxybutyl)(methyl)amino]-4-propylcyclohexan-1-ol
3-{[2-(Dimethylamino)ethyl](ethyl)amino}-4-propylcyclohexan-1-ol
5-(Methoxymethyl)-2-[(prop-2-yn-1-yl)carbamoyl]pyridine-3-carboxylic acid
5-(Methoxymethyl)-2-[(prop-2-en-1-yl)carbamoyl]pyridine-3-carboxylic acid
6-(2-aminocyclopropyl)-3-(methoxymethyl)-5H,6H,7H-pyrrolo[3,4-b]pyridine-5,7-dione
6-(2-aminopropyl)-3-(methoxymethyl)-5H,6H,7H-pyrrolo[3,4-b]pyridine-5,7-dione
2-(Hydroxymethyl)-5-(methoxymethyl)pyridine-3-carboxylic acid

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