82977-93-3

Usage

Uses

Used in Pharmaceutical Industry:
[R,(+)]-2-(Benzyloxy)propionyl chloride is used as a key intermediate for the synthesis of various pharmaceuticals and active ingredients. The benzyloxy group in the molecule makes it useful for creating compounds with specific properties and functions, contributing to the development of new drugs and medications.
Used in Agrochemical Production:
[R,(+)]-2-(Benzyloxy)propionyl chloride also has potential applications in the production of agrochemicals, where it can be used to create compounds with specific properties that can be beneficial in the agricultural sector.
Used in Flavor and Fragrance Industry:
Additionally, [R,(+)]-2-(Benzyloxy)propionyl chloride has potential uses in the flavor and fragrance industry, where it can be utilized to create unique scents and flavors for various products.
Safety Precautions:
Due to its high reactivity, [R,(+)]-2-(Benzyloxy)propionyl chloride must be handled and stored in accordance with proper safety protocols to ensure the safety of those working with it and to prevent any accidents or mishaps.

Upstream product

• 100836-85-9 (R)-2-benzyloxypropionic acid 

Downstream Products

• 119702-41-9 1-(1-Benzyloxy-ethyl)-cyclohexanol 
• 247196-90-3 Weinreb amide 
• 247196-88-9 C₁₆H₁₄F₂O₂ 
• 247196-89-0 (R)-2-benzyloxypropionyl N-morpholinyl amide 
• 1276682-92-8 C₂₄H₂₈N₂O₃ 
• 1276682-91-7 C₂₄H₂₈N₂O₃ 
• 1276682-85-9 C₂₄H₂₈N₂O₃ 
• 1276682-86-0 C₂₄H₂₈N₂O₃ 
• 114790-29-3 (R)-(dibenzyl) 3-(benzyloxy)-2-oxo-1-butyl phosphate 
• 100836-85-9 (R)-2-benzyloxypropionic acid 
• 159174-57-9 N-<(R)-2-benzyloxypropionyl>cyclo(-L-phenylalanyl-α-azaprolyl-) 
• 82939-03-5 N-<(R)-α-benzyloxypropionyl>-cyclo-(β-alanylprolyl) 
• 114790-28-2 (R)-3-(benzyloxy)-1-diazo-2-butanone 

Relevant academic research and scientific papers

NEW BIS ESTERS OF IVY SAPOGENINS FOR RUMINANTS

The present invention relates to synthetic bis esters of hederagenin, and their use in ruminants to improve ruminant growth performance, reduce rumen methane emission, reduce urine ammonia excretion, and/or to reduce rumen acetate to propionate ratio. Moreover, it also relates to a feed composition for ruminants comprising bis esters of hederagenin, and to novel bis esters of hederagenin.

Design, synthesis, and preliminary pharmacological evaluation of new quinoline derivatives as nicotinic ligands

A series of nicotinic ligands, carrying a quinoline nucleus, and characterized by a pharmacophoric distance between the quinoline nitrogen (H-bond acceptor) and the cationic nitrogen atoms higher than that proposed in the classical pharmacophoric models,

Process for the preparation of 2-hydroxyalkyl halophenones

2-Benzyloxyalkyl halophenones of the formula (3): wherein X1and X2are each independently H, Cl or F, provided that at least one of X1and X2is Cl or F; one of R3and R4is H and the other is optionally substituted benzyloxy; and R5is an unsubstituted alkyl, preferably a C1-6alkyl group. The compounds are useful as intermediates for preparing 2-hydroxyalkyl halophenones.