58966-34-0

Basic information

• Product Name: 5-Chloro-2-methylbenzaldehyde
• Synonyms: 5-Chloro-2-methylbenzaldehyde;3-Chloro-6-methylbenzaldehyde
• CAS NO: 58966-34-0
• Molecular Formula: C₈H₇ClO
• Molecular Weight: 154.59358
• Mol File: 58966-34-0.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 233℃
• Flash Point: 105℃
• Appearance: /
• Density: 1.195
• Vapor Pressure: 0.0581mmHg at 25°C
• Refractive Index: 1.562
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 5-Chloro-2-methylbenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Chloro-2-methylbenzaldehyde(58966-34-0)
• EPA Substance Registry System: 5-Chloro-2-methylbenzaldehyde(58966-34-0)

Safety Data

• Hazardous Substances Data: 58966-34-0(Hazardous Substances Data)

Usage

General Description

5-Chloro-2-methylbenzaldehyde is a chemical compound that belongs to the class of organic compounds known as chlorobenzenes. It has the molecular formula C8H7ClO and the molecular weight 154.59 g/mol. This chemical is slightly soluble in water, but readily soluble in most organic solvents. It is used in the synthesis of other chemicals, and is primarily designed for industrial use. However, like many other chemicals, it must be handled with care as it may present several hazards to health and the environment if not managed properly.

InChI:InChI=1/C8H7ClO/c1-6-2-3-8(9)4-7(6)5-10/h2-5H,1H3

Upstream product

• 39087-23-5 (4-Chloro-benzyl)-dimethyl-phenylsulfanylmethyl-ammonium; chloride 
• 75-17-2 formaldoxime 
• 615-65-6 2-chloro-4-methyl-benzenamine 
• 27139-97-5 2-bromo-4-chloro-1-methyl-benzene 
• 68-12-2 N,N-dimethyl-formamide 
• 611-74-5 N,N-dimethylbenzamide 
• 33184-48-4 4-chloro-2-iodotoluene 
• 2591-86-8 N-Formylpiperidine 
• 4885-02-3 Dichloromethyl methyl ether 
• 106-43-4 para-chlorotoluene 
• 104-83-6 1-Chloro-4-(chloromethyl)benzene 

Downstream Products

• 1093865-34-9 ethyl 3-{(R)-(5-chloro-2-methylphenyl)[(2-{[(methyloxy)carbonyl]amino}ethyl)oxy]methyl}benzoate 
• 1093865-29-2 ethyl 3-{(5-chloro-2-methylphenyl)[(2-{{[(1,1-dimethylethyl)oxy]carbonyl}[(methyloxy)carbonyl]amino}ethyl)oxy]methyl}benzoate 
• 1093865-32-7 ethyl 3-{(R)-(5-chloro-2-methylphenyl)[(2-{{[(1,1-dimethylethyl)oxy]carbonyl}[(methyloxy)carbonyl]amino}ethyl)oxy]methyl}benzoate 
• 1093865-93-0 C₁₉H₂₀ClIO₃ 
• 1093865-28-1 ethyl 3-[[(2-bromoethyl)oxy](5-chloro-2-methylphenyl)methyl]benzoate 
• 1352802-92-6 5-chloro-2-methylbenzaldehyde tert-butylimine 
• 1352803-33-8 7-chloro-1-fluoro-3-(3-fluorophenyl)isoquinoline 
• 1352803-34-9 N-tert-butyl-7-chloro-3-(3-fluorophenyl) isoquinolin-1-amine 
• 1001332-45-1 1-(5-chloro-2-methyl-phenyl)-3-trimethylsilyloxy-2-aza-1,3-butadiene 
• 1093865-27-0 ethyl 3-[(5-chloro-2-methylphenyl)(hydroxy)methyl]benzoate 
• 239132-34-4 4-(5-chloro-2-methylphenyl)-3-buten-2-one 
• 58630-80-1 7-chloro-4-methyl-indan-1-one 
• 900027-20-5 5-Chlor-2-methyl-hydrozimtsaeure 
• 58966-30-6 Ethyl-2-methyl-5-chlorbenzylsulfon 

Relevant articles and documents

Large-steric-hindrance triarylmethane derivative and synthesis method thereof

The invention provides a large-steric-hindrance triarylmethane derivative which has a general formula as shown in a compound (1) which is described in the specification. In the general formula, R1 isa C1-C6 alkyl group or C1-C6 alkoxy group; R2 is a C1-C6 alkyl group or C1-C6 alkoxy group; R3 is a C1-C6 alkyl group; R4 is independently selected from hydrogen, a methyl group, a methoxy group, halogen, a halogen substituted methyl group, a phenyl group and a naphthyl group; R5 is independently selected from hydrogen, a methyl group, a methoxy group, halogen, a halogen substituted methyl group,a phenyl group and a naphthyl group; R6 is respectively independent hydrogen, a methyl group, a methoxy group, halogen, a halogen substituted methyl group, a phenyl group and a naphthyl group; and X is halogen. The method has the advantages of simple operation, cheap and easily available raw materials, and suitableness for mass production.

Secondary Amines as Renin Inhibitors

The invention relates to novel secondary amine derivatives of formula (I) and the use thereof as active ingredients in the preparation of pharmaceutical compositions. The invention also concerns related aspects including processes for the preparation of the compounds, pharmaceutical compositions containing one or more of those compounds and especially their use as inhibitors of renin.

SECONDARY AMINES AS RENIN INHIBITORS

The invention relates to novel secondary amine derivatives of formula (I) and the use thereof as active ingredients in the preparation of pharmaceutical compositions. The invention also concerns related aspects including processes for the preparation of the compounds, pharmaceutical compositions containing one or more of those compounds and especially their use as inhibitors of renin.