70963-39-2

Basic information

• Product Name: N-ME-TYR-OME HCL
• Synonyms: (S)-2-(METHYL-AMINO)-3-(4-HYDROXY-PHENYL)-PROPIONIC ACID METHYL ESTER HCL;N-ME-TYR-OME HCL;N2-METHYL-L-TYROSINE METHYL ESTER HCL;(S)-2-(Me;N-Me-Tyr-OMe;N-methyl-L-tyrosine methyl ester
• CAS NO: 70963-39-2
• Molecular Formula: C₁₁H₁₅NO₃
• Molecular Weight: 245.7
• Mol File: 70963-39-2.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• Storage Temp.: Store at 0°C
• CAS DataBase Reference: N-ME-TYR-OME HCL(CAS DataBase Reference)
• NIST Chemistry Reference: N-ME-TYR-OME HCL(70963-39-2)
• EPA Substance Registry System: N-ME-TYR-OME HCL(70963-39-2)

Safety Data

• Hazardous Substances Data: 70963-39-2(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 537-49-5 N-methyl-L-tyrosine 
• 866392-22-5 N-benzyl-N-methyl-L-tyrosine methyl ester 
• 4326-36-7 (S)-N-(tert-butoxycarbonyl)tyrosine methyl ester 
• 112196-58-4 (S)-methyl-2-((tert-butoxycarbonyl)(methyl)amino)-3-(4-((tert-butyldimethyl-silyl)oxy)phenyl)propanoate 
• 112196-57-3 methyl (S)-2-((tert-butoxycarbonyl)amino)-3-(4-((tert-butyldimethylsilyl)-oxy)phenyl)propanoate 
• 60-18-4 L-tyrosine 
• 3417-91-2 L-tyrosine methyl ester HCl 
• 64263-81-6 N-(tert-butyloxycarbonyl)-N-methyl-O-(phenylmethyl)-L-tyrosine 
• 2130-96-3 O-benzyl-N-tert-butoxycarbonyl-L-tyrosine 
• 174906-30-0 methyl (S)-N-benzyl-L-tyrosinate 
• 69955-04-0 methyl N-benzylidene-tyrosinate 
• 1080-06-4 L-Tyr-OMe 
• 111934-14-6 (S)-2-(2-Aza-bicyclo[2.2.1]hept-5-en-2-yl)-3-(4-hydroxy-phenyl)-propionic acid methyl ester 

Downstream Products

• 84254-47-7 methyl N-boc-N-methyl-L-tyr-N-methyl-L-tyrosinate 
• 112196-59-5 methyl N-(tert-butoxycarbonyl)-N-methyl-L-tyrosinate 
• 113982-07-3 methyl 3-bromo-5-chloro-N-methyl-L-tyrosinate 
• 172036-67-8 methyl N-Boc-3-bromo-N-methyl-L-tyrosinate 
• 113982-06-2 methyl N-Boc-3-bromo-5-chloro-N-methyl-L-tyrosinate 
• 114014-11-8 methyl N-Cbz-3,5-dichloro-N-methyl-L-tyrosyl-3-bromo-5-chloro-N-methyl-L-tyrosinate 
• 91502-34-0 cyclo-N-methyl-L-tyr-N-methyl-L-tyr-D-ala-L-ala-O,N-dimethyl-L-tyr-L-ala 
• 91474-96-3 N-boc-N-methyl-L-tyr-N-methyl-L-tyr 
• 91502-35-1 methyl N-methyl-L-tyr-N-methyl-L-tyr-D-ala-L-ala-O,N-dimethyl-L-tyr-L-alaninate 
• 91475-02-4 methyl N-boc-N-methyl-L-tyr-N-methyl-L-tyr-D-ala-L-ala-O,N-dimethyl-L-tyr-L-alaninate 
• 112196-67-5 C₄₆H₅₁F₅N₆O₁₀*C₂HF₃O₂ 
• 112196-60-8 H-N-Me-Tyr-N-Me-Tyr-OMe 
• 112196-62-0 Boc-D-Ala-Ala-N-Me-Tyr(OMe)-Ala-N-Me-Tyr-N-Me-Tyr-OH 
• 112196-61-9 Boc-D-Ala-Ala-N-Me-Tyr(OMe)-Ala-N-Me-Tyr-N-Me-Tyr-OMe 

Relevant articles and documents

Facile synthesis of highly functionalized N-methyl amino acid esters without side-chain protection

(Chemical Equation Presented) The facile, two-pot synthesis of N-methyl amino acid esters by way of reductive amination is presented. Side chain protection schemes are not required, the starting materials are all commercially available, and the synthetic

Immonium Ion Based Synthetic Methodology: A Novel Method for the N-Methylation of Dipeptides and Amino Acid Derivatives via Retro Aza Diels-Alder Reactions

A novel method for the N-methylation of amino acid derivatives and dipeptides is detailed that features facile room-temperature retro Diels-Alder reactions of N-substituted 2-azanorbornenes with trapping of the incipient immonium ion with triethylsilane/trifluoroacetic acid.

Tumor-resolving and histolytic medicaments and their use

Dehydrooligopeptides, some of which are known, demonstrate histolytic and tumor-resolving activity and may be used in medicaments causing the lysis of animal tissues and/or tumors in warm-blooded animals.