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Z-L-Tyr-L-Ala-OMe is a tripeptide derivative, consisting of three amino acids: Z-protected L-tyrosine, L-alanine, and an O-methyl group. The Z group (benzyloxycarbonyl) is a protecting group used in peptide synthesis to prevent unwanted side reactions, while the O-methyl group is attached to the terminal amino acid, making it a C-terminally modified peptide. This specific sequence and structure give Z-L-Tyr-L-Ala-OMe unique properties and potential applications in various fields, such as pharmaceuticals, research, and drug development.

16874-62-7

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16874-62-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16874-62-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,7 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16874-62:
(7*1)+(6*6)+(5*8)+(4*7)+(3*4)+(2*6)+(1*2)=137
137 % 10 = 7
So 16874-62-7 is a valid CAS Registry Number.

16874-62-7Downstream Products

16874-62-7Relevant academic research and scientific papers

COMPOUNDS FOR AMIDE-FORMING REACTIONS

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Page/Page column 11; 18; 29; 30, (2014/01/07)

Provided herein is a compound of Formula I, that displays remarkable physicochemical properties as a peptide-coupling additive for peptide-forming reactions in water, wherein said coupling reactions proceed without measurable racemization. A method of pro

A new oxyma derivative for nonracemizable amide-forming reactions in water

Wang, Qinghui,Wang, Yong,Kurosu, Michio

supporting information; experimental part, p. 3372 - 3375 (2012/09/07)

An Oxyma derivative, (2,2-dimethyl-1,3-dioxolan-4-yl)methyl 2-cyano-2-(hydroxyimino)acetate (2), displayed remarkable physicochemical properties as a peptide-coupling additive for peptide-forming reactions in water. Short peptides to oligopeptides could b

Design, synthesis, and application of enantioselective coupling reagent with a traceless chiral auxiliary

Kolesinska, Beata,Kaminski, Zbigniew J.

supporting information; experimental part, p. 765 - 768 (2009/09/06)

(Chemical Equation Presented) Stable chiral N-triazinylbrucinium tetrafluoroborate enantioselectively activates racemic carboxylic acids yielding enantiomerically enriched amides, esters, and dipeptides with er from 8:92 to 0.5:99.5. Due to the departure

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