83509-86-8

Upstream product

• 2835-82-7 3-aminobutyric acid 
• 98-88-4 benzoyl chloride 

Downstream Products

• 83460-82-6 β-benzamidobutyranilide 
• 83460-81-5 ethyl R,S-β-benzamidobutyrate 
• 125558-95-4 4,5-dihydro-4-methyl-2-phenyl-1,3-oxazin-6-one 
• 61247-78-7 (E)-N-(4-phenylbut-3-en-2-yl)benzamide 
• 112979-60-9 (u,u)-3-<1'-(Benzoylamino)ethyl>-4-phenyloxetan-2-on 
• 121006-10-8 (u,u)-3-(Benzoylamino)-2-(1'-hydroxybenzyl)buttersaeure 
• 210103-07-4 D,L N-benzoyl-3-aminobutyric acid 2-propenyl ester 
• 210103-03-0 D,L N-benzoyl-3-aminobutyric acid cyclohexyl ester 
• 214903-09-0 DL-N-benzoyl-3-aminobutyric Acid N-octyl-ester 

Relevant academic research and scientific papers

Methods and compositions to protect crops against plant parasitic nematodes

A method for protecting a crop against plant-parasitic nematode attack by inducing local and systemic resistance of the crop comprising the application of a composition containing an effective amount of β-amino butyric acid or derivatives thereof to the c

Method for protecting plants from fungal infection

A method for protecting a crop against fungal diseases by inducing local and systemic resistance of the crop comprising applying to the crop or its locus a composition containing an effective amount of at least one β-aminobutyric acid or β-amino valeric a

A facile and stereocontrolled synthesis of syn-α-alkyl α-hydroxy β-amino acids

The diastereoselective synthesis of syn-α-alkyl α-hydroxy β-amino acids 4a-h was easily accomplished by reaction of the sodium dianion of the corresponding anti α-alkyl β-benzoylamino acid methyl esters with iodine. The intermediate α-iodo derivatives spontaneously afforded cis-oxazolines which, upon hydrolysis, provided the desired products, with diastereoselectivities up to 99:1.

Method to protect plants from fungal infection

A method for protecting a crop against fungal diseases by inducing local and systemic resistance of the crop comprising applying to the crop or its locus a composition containing an effective amount of a β-aminobutyric acid or β-amino valeric acid and der

194. Diastereoselecktive Alkylation of 3-Aminobutanoic Acid in the 2-Position

The enantiomerically pure 3-aminobutanoic acids (R)- and (S)-6 are readily available by preparative HPLC separation of the two diastereoisomers 5 obtained from addition of (S)-phenethylamine to methyl crotonate and subsequent hydrogenolysis (Scheme 2). (S)-methyl 3-(benzoylamino)butanoate ((S)-3) is also available by enzymatic kinetic resolution with pig-liver esterase.The N-benzoyl- and N-benzyloxycarbonyl derivatives rac-3, 8,and 9 of 3-aminobutanoates are doubly deprotonated with LDA and alkylated or aminated in high selectivity (17 examples, relative topicity like; see Tables 1 and 2).The configuration of three of the products is assigned (Schemes 4-6), and in four cases, the free α-substituted β-amino acid is prepared by acidic hydrolysis (see Table 3).It is shown that the doubly lithiated β-amino-acid derivative is solubilized, and its reactivity may be strongly influenced by the presence of 3 equiv. of LiCl.

Composition containing a penem or carbapenem antibiotic and the use of the same

Administration of an N-acylated amino acid in association with a penem or carbapenem antibiotic relieves or eliminates the renal problems associated with administration of the antibiotic alone. The amino acid derivative and antibiotic may be formulated together as a composition or administered separately, either simultaneously or sequentially.

Composition containing a penem or carbapenem antibiotic

Administration of an N-acylated amino acid in association with a penem or carbapenem antibiotic relieves or eliminates the renal problems associated with administration of the antibiotic alone. The amino acid derivative and antibiotic may be formulated together as a composition or administered separately, either simultaneously or sequentially. The composition may be prepared by simple mixing.