140434-48-6

Basic information

• Product Name: 1,9-Nonanediol, monobenzoate
• CAS NO: 140434-48-6
• Molecular Formula: C16H24O3
• Molecular Weight: 264.365
• Mol File: 140434-48-6.mol

Chemical Properties

• CAS DataBase Reference: 1,9-Nonanediol, monobenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: 1,9-Nonanediol, monobenzoate(140434-48-6)
• EPA Substance Registry System: 1,9-Nonanediol, monobenzoate(140434-48-6)

Safety Data

• Hazardous Substances Data: 140434-48-6(Hazardous Substances Data)

Upstream product

• 3937-56-2 1,9-Nonanediol 
• 98-88-4 benzoyl chloride 
• 1122-58-3 dmap 
• 1118635-09-8 (E)-benzoic acid 8-carboxy-oct-7-enyl ester 
• 201230-82-2 carbon monoxide 

Downstream Products

• 1157865-24-1 PhCO₂(CH₂)9F 
• 140434-49-7 benzoic acid 9-oxo-nonyl ester 
• 162129-96-6 8-(Methoxycarbonyl)octyl 2,3,4-tri-O-acetyl-6-O-trityl-α-D-mannopyranoside 
• 109681-59-6 8-methoxycarbonyloctyl 4,6-O-benzylidene-α-D-mannopyranoside 
• 110524-42-0 8-(Methoxycarbonyl)octyl 2,3,4,6-tetra-O-acetyl-α-D-mannopyranoside 
• 77666-97-8 8-(methoxycarbonyl)octyl α-D-mannoipyranoside 
• 76436-70-9 Methyl 9-benzoyloxynonanoate 
• 162130-01-0 9-(benzoyloxy)nonanoic acid 

Relevant articles and documents

Tandem decarboxylative hydroformylation-hydrogenation reaction of α,β-unsaturated carboxylic acids toward aliphatic alcohols under mild conditions employing a supramolecular catalyst system

A new atom economic catalytic method for a highly chemoselective reduction of α,β-unsaturated carboxylic acids to the corresponding saturated alcohols under mild reaction conditions, compatible with a wide range reactive functional groups, is reported. The new methodology consists of a novel tandem decarboxylative hydroformylation/aldehyde reduction sequence employing a unique supramolecular catalyst system.

One-pot synthesis of imidazolines from aldehydes: detailed study about solvents and substrates

Imidazolines were prepared in one-pot operation from aldehydes and diamines through oxidation of aminal intermediates by NBS. This method could be applied to various aromatic and aliphatic aldehydes and N-nonsubstituted and N-monosubstituted 1,2-diamines. Furthermore, it was found that CH2Cl2 could be altered to TBME, a more environmentally friendly solvent, in the reaction using N-nonsubstituted 1,2-diamines. The reaction conditions were very mild and chemoselective.

A mild and selective cleavage of p-methoxybenzyl Ethers by CBr4-MeOH

p-Methoxybenzyl ethers were selectively deprotected to the corresponding alcohols and phenols in high yields by CBr4 in refluxing methanol under neutral reaction conditions.

SYNTHESIS OF IMMUNOSUPPRESIVE NEOGLYCOPROTEINS: BOVINE SERUM ALBUMIN COUPLED WITH 8-(HYDRAZINOCARBONYL)OCTYL 4- OR 6-O-&α-D-MANNOPYRANOSYL-&α-D-MANNOPYRANOSIDE

Recombinant cytokines generated by bacteria, especially E.coli, are nonglycosylated.To investigate the effects of carbohydrates on their activities, we attempted to develop new cytokines by introduction of carbohydrates.As a model we synthesized neoglycop

Pesticidal polyhalo alkenoic acid esters

The present invention discloses and exemplifies alcohol, ether and ester derivatives of difluoroalkanes and difluoroalkenylalkanes having the general formula R--(CH2)m --CR2 R3 --OR1, in which R is a 1,1-difluoroalkyl or a 1,1-difluoroalkenyl group, composition thereof, and use thereof to control agricultural crop pests.