70601-62-6

Basic information

• Product Name: AC-D-TYR(ME)-OH
• Synonyms: AC-D-TYR(ME)-OH;AC-D-PHE(4-OME)-OH;ACETYL-4-METHOXY-D-PHENYLALANINE;ACETYL-O-METHYL-D-TYROSINE;N-ALPHA-ACETYL-D-(4-METHOXY)TYROSINE;N-ALPHA-ACETYL-O-METHYL-D-TYROSINE;N-Acetyl-O-methyl-D-tyrosine
• CAS NO: 70601-62-6
• Molecular Formula: C₁₂H₁₅NO₄
• Molecular Weight: 237.25
• Mol File: 70601-62-6.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: AC-D-TYR(ME)-OH(CAS DataBase Reference)
• NIST Chemistry Reference: AC-D-TYR(ME)-OH(70601-62-6)
• EPA Substance Registry System: AC-D-TYR(ME)-OH(70601-62-6)

Safety Data

• Hazardous Substances Data: 70601-62-6(Hazardous Substances Data)

Usage

General Description

AC-D-TYR(ME)-OH is a chemical compound that is a modified form of the amino acid tyrosine. The "AC-D" prefix indicates that it is a derivative of the amino acid, and the "(ME)" denotes that it contains a methyl group. This modification can alter the chemical and biological properties of tyrosine, potentially affecting its interactions with other molecules and biological processes. The compound AC-D-TYR(ME)-OH may have potential applications in research and drug development, particularly in the study of protein structure and function, as well as in the development of pharmaceuticals targeting specific biological pathways.

Upstream product

• 73549-09-4 (Z)-2-acetamido-3-(4-methoxyphenyl)-2-propenoic acid 
• 7635-29-2 O-methyl tyrosine 
• 108-24-7 acetic anhydride 
• 6318-42-9 5-(4-methoxy-benzyl)-hydantoin 
• 71198-72-6 4-[(4-methoxyphenyl)methylene]-2-methyl-5(4H)-oxazolone 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 39878-65-4 (R)-β-(4-methoxyphenyl)alanine 
• 162465-45-4 (R)-2-((tet-butoxycarbonyl)amino)-3-(3-chloro-4-methoxyphenyl)propanoic acid 
• 124689-64-1 cryptophycin C 
• 124689-65-2 cryptophycin-1 
• 179093-50-6 (S)-2-{(R)-3-[(R)-2-tert-Butoxycarbonylamino-3-(3-chloro-4-methoxy-phenyl)-propionylamino]-2-methyl-propionyloxy}-4-methyl-pentanoic acid 
• 182486-25-5 tert-butyl (5S,6R)-5-[(2S)-2-[(2R)-3-[(2R)-2-tert-butoxycarbonylamino-3-(3-chloro-4-methoxyphenyl)propionylamino]-2-methylpropionyloxy]-4-methylpentanoyloxy]-6-methyl-8-phenylocta-2(E),7(E)-dienoate 
• 196794-47-5 benzyl (2S)-2-[(2R)-3-[(2R)-2-tert-butoxycarbonylamino-3-(3-chloro-4-methoxyphenyl) propionylamino]-2-methylpropionyloxy]-4-methylpentanoate 
• 178977-43-0 (S)-2-{3-[(R)-2-tert-Butoxycarbonylamino-3-(3-chloro-4-methoxy-phenyl)-propionylamino]-propionyloxy}-4-methyl-pentanoic acid 
• 245125-86-4 benzyl (2S)-2-[3-[(2R)-2-tert-butoxycarbonylamino-3-(3-chloro-4-methoxyphenyl)propionylamino]propionyloxy]-4-methylpentanoate 
• 245125-91-1 tert-butyl (5S,6R)-5-[(2S)-2-[3-[(2R)-2-(tert-butoxycarbonylamino)-3-(3-chloro-4-methoxyphenyl)propionylamino]propionyloxy]-4-methylpentanoyloxy]-6-methyl-8-phenylocta-2(E),-7(E)-dienoate 
• 70601-63-7 (D)-4-methoxyphenylalanine hydrochloride 

Relevant articles and documents

Asymmetric synthesis of unnatural amino acids and tamsulosin chiral intermediate

An efficient and enantioselective hydrogenation of N-acetylamino phenyl acrylic acids was successfully developed by using ruthenium catalyst. This methodology is important in the field of pharmaceuticals and provides a new process for the preparation of unnatural amino acids and tamsulosin chiral intermediate.

Electronic and steric effects of ligands as control elements for rhodium-catalyzed asymmetric hydrogenation

Chiral diphosphine ligands analogous to bdpp have been synthesized and tested in order to study the effect of the electronic nature of the ligands in Rh-catalyzed asymmetric hydrogenation of some prochiral olefins. The results are compared with those obtained with the analogous unsubstituted ligand (bdpp). The rhodium-catalyzed asymmetric hydrogenation of olefins was influenced by ligand-based electronic effects, as well as substrate based ones. Excellent ee's (up to 98.3%) have been obtained in the rhodium-catalyzed hydrogenation of (Z)-α-acetamidocinnamic acids and esters.

Highly enantioselective rhodium-catalyzed hydrogenation of dehydroamino acids with new chiral bisphosphinites

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