23234-83-5

Basic information

• Product Name: L-Leucine, N-[[(4-methoxyphenyl)methoxy]carbonyl]-
• CAS NO: 23234-83-5
• Molecular Formula: C15H21NO5
• Molecular Weight: 295.335
• Mol File: 23234-83-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: L-Leucine, N-[[(4-methoxyphenyl)methoxy]carbonyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: L-Leucine, N-[[(4-methoxyphenyl)methoxy]carbonyl]-(23234-83-5)
• EPA Substance Registry System: L-Leucine, N-[[(4-methoxyphenyl)methoxy]carbonyl]-(23234-83-5)

Safety Data

• Hazardous Substances Data: 23234-83-5(Hazardous Substances Data)

Upstream product

• 18912-37-3 4-methoxybenzyl hydrazinecarboxylate 
• 31558-46-0 4-methoxybenzyl phenyl carbonate 
• 75-44-5 phosgene 
• 61-90-5 L-leucine 
• 105-13-5 4-Methoxybenzyl alcohol 
• 145126-14-3 Moz-Leu-OBzl 
• 25474-85-5 4-methoxybenzyloxycarbonyl azide 

Downstream Products

• 101301-24-0 Z(OMe)-Leu-Leu-NHNH₂ 
• 101301-23-9 Z(OMe)-Leu-Leu-OMe 
• 74105-06-9 Z(OMe)-Lys(Z)-Lys(Z)-Leu-Leu-NH₂ 
• 74105-09-2 Z(OMe)-Met(O)-Ala-Lys(Z)-Lys(Z)-Leu-Leu-NH₂ 
• 101301-25-1 Z(OMe)-Leu-Leu-Gln-Gly-Leu-Val-NH₂ 
• 101301-28-4 Z(OMe)-Gln-Arg(Mts)-Leu-Leu-Gln-Gly-Leu-Val-NH₂ 
• 80516-89-8 {(S)-1-[(S)-1-((S)-1-Azidocarbonyl-2-methyl-propylcarbamoyl)-2-(1H-imidazol-4-yl)-ethylcarbamoyl]-3-methyl-butyl}-carbamic acid 4-methoxy-benzyl ester 
• 80503-77-1 Z(OMe)-Leu-His-Val-NHNH₂ 
• 80503-76-0 Z(OMe)-Leu-His-Val-OMe 
• 80503-75-9 {(S)-1-[(S)-1-Azidocarbonyl-2-(1H-imidazol-4-yl)-ethylcarbamoyl]-3-methyl-butyl}-carbamic acid 4-methoxy-benzyl ester 
• 80503-74-8 Z(OMe)-Leu-His-NHNH₂ 
• 90984-58-0 Z(OMe)-Leu-Gln-Asp(OBzl)-Ile-Met(O)-NHNH-Troc 
• 90984-59-1 Z(OMe)-Leu-Gln-Asp(OBzl)-Ile-Met(O)-NHNH₂ 
• 148529-00-4 Boc-Orn(Boc)-Phe-Phe-Gly-Leu-Nva(5-OBzl)-NH₂ 

Relevant articles and documents

Studies of peptide antibiotics. XIX. Syntheses of 1,1'-leucine-gramicidin S and 1-leucine-cyclosemigramicidin S.

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Use of 2-pyrimidine thiol carbonates as acylating agents for amino or imino containing compounds

Thiolcarbonates represented by the formula, SPC1 Wherein R1 and R2 are individually a hydrogen atom or a methyl group, and R3 is a straight chain or branched chain saturated or unsaturated alkyl group having 1 to 5 carbon atoms or is a benzyl or benzhydryl group which may be nuclear substituted, are quite useful for protecting the amino or imino groups of amines, hydrazines, amino acids and peptides with groups of the formula EQU1 The thiolcarbonates can be easily produced by reacting an alkali metal salt of 2-mercaptopyrimidine with phosgene, and reacting the resulting thiolchloroformate with an alcohol (R3 OH), or by reacting a 2-mercaptopyrimidine with a halocarbonic acid ester.