115787-51-4

Basic information

• Product Name: Benzaldehyde, 5-(chloroacetyl)-2-hydroxy- (9CI)
• Synonyms: Benzaldehyde, 5-(chloroacetyl)-2-hydroxy- (9CI);5-(2-chloroacetyl)-2-hydroxybenzaldehyde;Benzaldehyde, 5-(chloroacetyl)-2-hydroxy-;5-(Chloroacetyl)-2-hydroxybenzaldehyde
• CAS NO: 115787-51-4
• Molecular Formula: C₉H₇ClO₃
• Molecular Weight: 198.60308
• Product Categories: ACETYLHALIDE
• Mol File: 115787-51-4.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 366.6±32.0 °C(Predicted)
• Appearance: /
• Density: 1.394±0.06 g/cm3(Predicted)
• PKA: 5.96±0.20(Predicted)
• CAS DataBase Reference: Benzaldehyde, 5-(chloroacetyl)-2-hydroxy- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzaldehyde, 5-(chloroacetyl)-2-hydroxy- (9CI)(115787-51-4)
• EPA Substance Registry System: Benzaldehyde, 5-(chloroacetyl)-2-hydroxy- (9CI)(115787-51-4)

Safety Data

• Hazardous Substances Data: 115787-51-4(Hazardous Substances Data)

Usage

General Description

Benzaldehyde, 5-(chloroacetyl)-2-hydroxy- (9CI) is a chemical compound with the molecular formula C9H9ClO2. It is a chloroacetyl derivative of benzaldehyde, and has a hydroxy group attached to the 2nd carbon in the benzene ring. Benzaldehyde, 5-(chloroacetyl)-2-hydroxy- (9CI) is commonly used in organic synthesis and chemical reactions to create various pharmaceuticals, flavors, and fragrances. It is also used as an intermediate in the production of pesticides, dyes, and other fine chemicals. Additionally, benzaldehyde, 5-(chloroacetyl)-2-hydroxy- (9CI) has been studied for its potential pharmaceutical properties, including its antibacterial and antiviral effects.

Upstream product

• 22118-09-8 2-bromoacetyl chloride 
• 90-02-8 salicylaldehyde 
• 79-04-9 chloroacetyl chloride 

Downstream Products

• 115787-57-0 2-Chloro-1-<3-<<(1,1-dimethylethyl)imino>methyl>-4-hydroxyphenyl>ethanone 
• 18559-94-9 Salbutamol 
• 115787-53-6 5-<<(1,1-Dimethylethyl)amino>acetyl>-2-hydroxybenzaldehyde hydrochloride 
• 115787-52-5 5-(2-tert-Butylamino-acetyl)-2-hydroxy-benzaldehyde 
• 1332862-61-9 (S)-2,2-dimethyl-6-(oxiran-2-yl)-4H-benzo[1,3]dioxin 
• 1332862-57-3 2-chloro-1-(4-hydroxy-3-(hydroxymethyl)phenyl)ethanone 
• 35459-11-1 (S)-salbutamol acetate 

Relevant articles and documents

A chromatography-free synthesis of racemic salbutamol hemisulfate

Our efforts to achieve an efficient synthesis of racemic salbutamol hemisulfate are described. The selected chemical route starts from commodity chemicals and allows the generation of salbutamol hemisulfate in 5 steps and 44% overall yield without any purification by column chromatography. The reaction sequence has been optimized to provide the title compound using robust procedures. Emphasis on reproducibility and experimental simplicity drove the work described herein.

SUBSTITUTED HYDRAZIDE COMPOUNDS AND APPLICATION THEREOF

The invention relates to substituted hydrazide compounds as shown by general formula I, including geometrical isomers, pharmaceutically acceptable salts, hydrates, solvates or prodrugs thereof, and use of the same, wherein the substitutents Ar and R having the same meanings as given in the Description. T The invention further relates to the use of compounds of general formula I in the preparation of medicament for the treatment and/or prevention of cancer and other proliferative diseases.

A short synthesis of albuterol

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