3717-23-5

Basic information

• Product Name: (Z)-4-Chlorobenzaldehyde oxime
• Synonyms: (Z)-4-Chlorobenzaldehyde oxime
• CAS NO: 3717-23-5
• Molecular Formula: C₇H₆ClNO
• Molecular Weight: 155.5816
• Mol File: 3717-23-5.mol
• Article Data: 15

Chemical Properties

• Boiling Point: 233.2°Cat760mmHg
• Flash Point: 94.8°C
• Appearance: /
• Density: 1.21g/cm³
• Vapor Pressure: 0.0314mmHg at 25°C
• Refractive Index: 1.55
• CAS DataBase Reference: (Z)-4-Chlorobenzaldehyde oxime(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-4-Chlorobenzaldehyde oxime(3717-23-5)
• EPA Substance Registry System: (Z)-4-Chlorobenzaldehyde oxime(3717-23-5)

Safety Data

• Hazardous Substances Data: 3717-23-5(Hazardous Substances Data)

Usage

General Description

(Z)-4-Chlorobenzaldehyde oxime, also known as p-chlorobenzaldoxime, is a compound with the molecular formula C7H6ClNO. It is an organic chemical that belongs to the class of benzaldoximes. (Z)-4-Chlorobenzaldehyde oxime is a white to slightly yellow solid at room temperature and is only slightly soluble in water. (Z)-4-Chlorobenzaldehyde oxime is mainly used as a chemical intermediate in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals. It also has potential applications in the field of organic chemistry as a reagent for certain chemical reactions. Additionally, this compound has been subject to research for its potential biological activities and pharmacological properties.

InChI:InChI=1/C7H6ClNO/c8-7-3-1-6(2-4-7)5-9-10/h1-5,10H/b9-5-

Upstream product

• 80055-48-7 4-chloro-benzaldehyde-(O-acetyl-seqcis-oxime ) 
• 104-88-1 4-chlorobenzaldehyde 
• 3717-24-6 4-chlorobenzaldehyde oxime 
• 71-43-2 benzene 

Downstream Products

• 3717-24-6 4-chlorobenzaldehyde oxime 
• 80055-48-7 4-chloro-benzaldehyde-(O-acetyl-seqcis-oxime ) 
• 619-56-7 4-chlorobenzamide 
• 130966-62-0 3-(4-chlorophenyl)-4-phenylisoxazole 
• 125674-27-3 Diethyl 3-(4-chlorophenyl)-2-isoxazolin-5-ylmethylphosphonate 
• 1140531-54-9 (E)-4-chlorobenzaldehyde O-1-(2-oxopyrrolidin-1-yl)ethyloxime 
• 1140531-55-0 (E)-4-chlorobenzaldehyde O-1-(azepan-2-on-1-yl)ethyloxime 
• 5300-92-5 5-(bromomethyl)-3-(4-chlorophenyl)-isoxazole 
• 105755-37-1 4-chlorobenzohydroximoyl chloride 
• 7050-86-4 4-chloro-benzaldehyde-(O-carbamoyl oxime ) 
• 104-86-9 4-chlorobenzylamine 
• 104-88-1 4-chlorobenzaldehyde 
• 623-03-0 4-Cyanochlorobenzene 
• 24515-81-9 3-(4-chloro-phenyl)-5-(2,2,2-trifluoro-1-trifluoromethyl-ethylidene)-[1,4,2]oxathiazolidine 

Relevant articles and documents

Host (dealuminated Y zeolite)–guest (zirconium tetraphenylporphyrin) nanocomposite materials. An efficient catalyst in the oximation of aldehydes

In this research, zirconium tetraphenylporphyrin encapsulated into dealuminated Y zeolite (ZrTPP–DAZY) was prepared through a template synthesis method. This heterogeneous catalyst was characterized by XRD, FT-IR, DRS, UV–Vis, EDX and FESEM techniques. The amount of ZrTPP in the nanocage of dealuminated Y zeolite was estimated to be 0.0156?g/g of support. This catalytic system was employed for an efficient oximation of aldehydes under magnetic stirring conditions at room temperature and the corresponding products were obtained in 50–90% yields. This catalytic system also indicated good shape selectivity towards linear aldehydes. ZrTPP–DAZY was reused several times without any significant loss in catalytic activity.

Catalytic performance of preyssler anion in selective oximation of aromatic aldehydes

Preyssler catalyst, H14[NaP5W30O110], catalyzes the aldoximation of aromatic aldehydes for the synthesis of Z-isomers in conventional manner and under microwave irradiation. Both pure acid and silica-supported catalysts were used and their activities compared with common catalysts such as K2CO3 and CuSO4. The Preyssler is the catalyst for this reaction.