82310-99-4

Upstream product

• 4521-28-2 4-(4-Methoxyphenyl)butyric acid 
• 82267-43-4 <4-(p-methoxyphenyl)butyl>(acetamido)malonic acid 
• 52244-70-9 4-(4-methoxyphenyl)butan-1-ol 
• 35191-43-6 1-(4-bromo-butyl)-4-methoxy-benzene 
• 82267-45-6 DL-2-acetamido-6-(p-methoxyphenyl)hexanoic acid 
• 82267-41-2 diethyl <4-(p-methoxyphenyl)butyl>(acetamido) malonate 

Downstream Products

• 92837-08-6 Boc-L-Ala-L-Hmb-L-Amh-OH 
• 92837-14-4 D-A₂pr(Z)-L-Ala-L-Hmb-L-Amh-ONSu trifluoroacetic acid 
• 92837-12-2 Boc-D-A₂pr(Z)-L-Ala-L-Hmb-L-Amh-ONSu 
• 92882-38-7 Boc-D-A₂pr(Z)-L-Ala-L-Hmb-L-Amh-OH 
• 92837-09-7 L-Ala-L-Hmb-L-Amh-OH hydrochloride 

Relevant academic research and scientific papers

Synthesis method of multi-configuration long-chain phenyl amino acid compound

The invention relates to a method for synthesizing a multi-configuration long-chain phenyl amino acid compound. The method comprises the following steps: reacting a compound shown in a formula I witha compound shown in a formula II or an isomer thereof in

PREPARATION OF HOMOLOGS OF L-2-AMINO-5-(p-METOXYPHENYL)PENTANOIC ACID

Lower and higher homologs, L-2-amino-4-(p-methoxyphenyl)butanoic acid (L-amb) and L-2-amino-6-(p-methoxyphenyl)hexanoic acid (L-Amh), of L-2-amino-5-(p-methoxyphenyl)pentanoic acid were prepared by optical resolution of N-acetyl-DL-Amb and of N-acetyl-DL-Amh with Aspergillus acylase.N-acetyl DL-Amb or N-acetyl-DL-Amh was synthesized from (acetamido malonic acid by heating with p-xylene.