95513-13-6

Basic information

• Product Name: Octanoic acid, 2-hydroxy-, phenylmethyl ester
• CAS NO: 95513-13-6
• Molecular Formula: C15H22O3
• Molecular Weight: 250.338
• Mol File: 95513-13-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Octanoic acid, 2-hydroxy-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Octanoic acid, 2-hydroxy-, phenylmethyl ester(95513-13-6)
• EPA Substance Registry System: Octanoic acid, 2-hydroxy-, phenylmethyl ester(95513-13-6)

Safety Data

• Hazardous Substances Data: 95513-13-6(Hazardous Substances Data)

Upstream product

• 13495-04-0 sodium 1-hydroxyheptane-1-sulfonate 
• 28870-09-9 2-hydroxy-octanoic acid amide 
• 66471-52-1 2-hydroxyoctanenitrile 
• 126543-34-8 ((Z)-1-Ethoxy-oct-1-enyloxy)-trimethyl-silane 
• 42512-94-7 α-Acetoxy-caprylsaeure-ethylester 
• 106-32-1 octanoic acid ethyl ester 
• 617-73-2 2-hydroxy-octanoic acid 
• 100-51-6 benzyl alcohol 
• 100-39-0 benzyl bromide 

Downstream Products

• 95513-28-3 (2S)-cis-1-(phenylsulfonyl)-2-(1-<(phenylsulfonyl)oxy>butyl)-5-heptylpyrrolidine 
• 95513-21-6 (2S)-cis-1-benzyl-5-heptylproline tert-butyl ester 
• 95513-23-8 (2S)-trans-1-benzyl-5-heptylproline tert-butyl ester 
• 95513-29-4 (2S)-cis-5-butyl-2-heptyl-1-(phenylsulfonyl)pyrrolidine 
• 95513-54-5 1-((2S,5S)-1-Benzyl-5-heptyl-pyrrolidin-2-yl)-butan-1-one 
• 95513-24-9 (2S)-cis-1-benzyl-5-heptylproline 
• 95513-25-0 (2S)-cis-1-benzyl-2-(1-hydroxybutyl)-5-heptylpyrrolidine 
• 95587-06-7 (2R,5S)-1-Benzyl-5-heptyl-pyrrolidine-2-carbonitrile 
• 95513-33-0 (2S,5S)-1-Benzyl-5-heptyl-pyrrolidine-2-carbonitrile 
• 95513-16-9 (2S)-1-benzyl-5-(1-<(benzyloxy)carbonyl>heptylidene)proline tert-butyl ester 
• 95513-39-6 (5S)-1-benzyl-2-butyl-5-heptylproline tert-butyl ester 
• 95513-27-2 (2S)-cis-1-(phenylsulfonyl)-2-(1-hydroxybutyl)-5-heptylpyrrolidine 
• 95513-41-0 (5S)-1-benzyl-2-butyl-5-heptylproline 
• 95587-05-6 cis-2-heptyl-5-butylpyrrolidine 

Relevant articles and documents

Novel acyl-dipeptide-like compounds bearing an accessory functional side chain spacer, a method for preparing the same and pharmaceutical compositions containing such products

The present invention is directed in particular to dipeptide-like compounds derived from functionally substituted amino acids, having fatty acid chains bound thereto through amidification of the amine functional groups of said dipeptide-like compounds, one end portion of which bears an accessory functional side chain spacer, with the other end portion being an acid group either in neutral or charged state. Compounds of the present invention have immunomodulating properties like adjuvants, In addition, compounds of the invention can be grafted on a given antigen in order to modulate or tune the immune response or can be equally grafted on a pharmaceutical carrier to enhance the therapeutic effect or targetting thereof. Accordingly, compounds of the invention find use in human and veterinary medicine both as immunogens and diagnostic tools.

Role of the hydrophobic moiety of tumor promoters. Synthesis and activity of 2-alkylated benzolactams

The size and position of a hydrophobic moiety on a benzolactam skeleton, which reproduces the active conformation and biological activity of teleocidins, play an important role in the appearance of the activity. Compounds with alkyl groups of various sizes and shapes at the 2-position of benzolactam were synthesized. Structure-activity results indicate that a hydrophobic substituent at the C-2 position plays a critical role in the appearance of biological activities, as in the case of substitution at C-9.