ChemicalBook > Product Catalog >Biochemical Engineering >Amino Acids and Derivatives >Fmoc-N-Me-Lys(Boc)-OH

Fmoc-N-Me-Lys(Boc)-OH

CAS No.: 197632-76-1

Chemical Name:: Fmoc-N-Me-Lys(Boc)-OH

Synonyms: FM;FM;FMOC-MELYS(BOC)-OH;FMOC-L-MELYS(BOC)-OH;FMOC-N-ME-LYS(BOC)-OH;FMoc-Nw-Me- Lys(Boc)-OH;FMOC-N-ME-LYS(BOC)-OH 1 G;Fmoc-Nω-Me-Lys(Boc)-OH, >97%;FMOC-N-ME-LYS(BOC)-OH 250 MG;N'-Cbz-N-Fmoc-N-methyl-L-lysine

CBNumber:: CB1473656

Molecular Formula:: C27H34N2O6

Molecular Weight:: 482.57

MOL File:: 197632-76-1.mol

MSDS File:: SDS

Modify Date:: 2024/7/2 8:55:01

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Fmoc-N-Me-Lys(Boc)-OH Properties

Melting point	189-194°C (decomposition)
Boiling point	665.4±55.0 °C(Predicted)
Density	1.200
storage temp.	2-8°C
form	Solid
pka	3.90±0.21(Predicted)
color	White to off-white
optical activity	[α]22/D -14.0°, c = 1% in chloroform
InChIKey	JMBKBGOKNZZJQA-QHCPKHFHSA-N
CAS DataBase Reference	197632-76-1

SAFETY

Risk and Safety Statements

Symbol(GHS)	GHS07
Signal word	Warning
Hazard statements	H315-H319-H335
Precautionary statements	P261-P305+P351+P338
WGK Germany	3
HazardClass	IRRITANT
HS Code	29242990

Fmoc-N-Me-Lys(Boc)-OH price More Price(4)

Manufacturer	Product number	Product description	CAS number	Packaging	Price	Updated	Buy
Sigma-Aldrich(India)	8.52361	Fmoc-N-Me-Lys(Boc)-OH Novabiochem?	197632-76-1	250MG	₹16460	2022-06-14	Buy
Sigma-Aldrich(India)	8.52361	Fmoc-N-Me-Lys(Boc)-OH Novabiochem?	197632-76-1	1G	₹49640	2022-06-14	Buy
Sigma-Aldrich(India)	773107	Fmoc-N-Me-Lys(Boc)-OH 97% (HPLC)	197632-76-1	250MG	₹12110	2022-06-14	Buy
Sigma-Aldrich(India)	773107	Fmoc-N-Me-Lys(Boc)-OH 97% (HPLC)	197632-76-1	1G	₹31840	2022-06-14	Buy

Product number	Packaging	Price	Buy
8.52361	250MG	₹16460	Buy
8.52361	1G	₹49640	Buy
773107	250MG	₹12110	Buy
773107	1G	₹31840	Buy

Fmoc-N-Me-Lys(Boc)-OH Chemical Properties,Uses,Production

Description

Fmoc-N-Me-Lys(Boc)-OH is a peptide that mimics the structure of the natural substrate of serine protease. It has been shown to be stable in extracellular fluids and resistant to proteolytic degradation. The systematic sequence was designed to maximize the chance of binding to the active site of serine proteases while minimizing binding to other proteases. The maximal modifications were made on the amino acid side chains, which are most likely to interact with other proteins or with cell surfaces.

Chemical Properties

white to slight yellow to beige

Fmoc-N-Me-Lys(Boc)-OH Preparation Products And Raw materials

Raw materials

Preparation Products

Fmoc-N-Me-Lys(Boc)-OH Suppliers

Global( 100)Suppliers

Supplier	Tel	Country	ProdList	Advantage	Inquiry
A.J Chemicals	91-9810153283	New Delhi, India	6124	58	Inquiry
CLEARSYNTH LABS LTD.	+91-22-45045900	Hyderabad, India	6351	58	Inquiry
Sichuan HongRi Pharma-Tech Co.,Ltd	+86-028-64841719 +8617390183901	China	1381	58	Inquiry
Alpha Biopharmaceuticals Co., Ltd	+86-15542445688	China	888	58	Inquiry
Capot Chemical Co.,Ltd.	571-85586718 +8613336195806	China	29798	60	Inquiry
Hangzhou FandaChem Co.,Ltd.	008657128800458; +8615858145714	China	9337	55	Inquiry
CONIER CHEM AND PHARMA LIMITED	+8618523575427	China	49391	58	Inquiry
Career Henan Chemica Co	+86-0371-86658258 +8613203830695	China	30253	58	Inquiry
Apeloa Pharmaceutical Co., Ltd.	+86-0571-87635730 +8615858229168	China	1478	58	Inquiry
BOC Sciences	16314854226; +16314854226	United States	19743	58	Inquiry

Supplier	Advantage
A.J Chemicals	58
CLEARSYNTH LABS LTD.	58
Sichuan HongRi Pharma-Tech Co.,Ltd	58
Alpha Biopharmaceuticals Co., Ltd	58
Capot Chemical Co.,Ltd.	60
Hangzhou FandaChem Co.,Ltd.	55
CONIER CHEM AND PHARMA LIMITED	58
Career Henan Chemica Co	58
Apeloa Pharmaceutical Co., Ltd.	58
BOC Sciences	58

197632-76-1(Fmoc-N-Me-Lys(Boc)-OH )Related Search:

N-Methyl-1-naphthalenemethylamine hydrochloride FMOC-N-METHYL-L-NORLEUCINE Fmoc-n-amido-peg10-acid Fmoc-S-trityl-alpha-Me-L-cysteine FMOC-N-Methyl-L-alanine

Fmoc-N-Me-Arg(pbf)-OH FMoc-N-Me-Lys(2-Cl-Z)-OH Boc-N-Me-Lys(N3)-OH Boc-N-Me-Lys(Fmoc)-OH Boc-N-Me-Lys(2-Cl-Z)-OH

Boc-N-Me-D-Lys(Fmoc)-OH Fmoc-N-methyl-L-isoleucine FMoc-N-Me-His(Trt)-OH (R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(4-(tert-butoxy)phenyl)propanoic acid FMOC-N-ME-ARG(MTR)-OH

Fmoc-N-methyl-L-glutamic acid 5-tert-butyl ester FMOC-SARCOSINE MONOHYDRATE Fmoc-N-methyl-L-phenylalanine

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N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-ALPHA-METHYL-N-EPSILON-T-BUTYL-OXYCARBONYL-L-LYSINE N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-ALPHA-METHYL-N-EPSILON-TERT-BUTYLOXYCARBONYL-L-LYSINE FMOC-N-ALPHA-METHYL-N-EPSILON-T-BOC-L-LYSINE FMOC-MELYS(BOC)-OH FMOC-N-ME-LYS(BOC)-OH FMOC-L-MELYS(BOC)-OH Fmoc-Nalpha-methyl-Ne-t-Boc-L-lysine N'-[(tert-Butoxy)carbonyl]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-methyl-L-lysine N6-[(1,1-Dimethylethoxy)carbonyl]-N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-N2-methyl-L-lysine N'-Cbz-N-Fmoc-N-methyl-L-lysine NA-FMOC-NA-METHYL-NE-BOC-L-LYSINE FMoc-Nw-Me- Lys(Boc)-OH N^e-Boc-N^a-FMoc-N^a-Methyl-L-lysine, 98% Nα-Fmoc-Nα-methyl-Nε-t-Boc-L-lysine N^α-FMoc-N^α-Methyl-N^ε-Boc-L-lysine (S)-2-((((9H-Fluoren-9-yl)Methoxy)carbonyl)(Methyl)aMino)-6-((tert-butoxycarbonyl)aMino)hexanoic acid N'-Boc-N-Fmoc-N-methyl-L-lysine N2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N6-(tert-butoxycarbonyl)-N2-methyl-L-lysine (2S)-6-{[(tert-butoxy)carbonyl]amino}-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}(methyl)amino)hexanoic acid (9H-Fluoren-9-yl)MethOxy]Carbonyl N-Me-Lys(Boc)-OH Fmoc-N-Me-Lys(Boc)-OH N-Fmoc-N'-Methyl-N'-Boc-Lysine Fmoc-Nω-Me-Lys(Boc)-OH, >97% FMOC-N-ME-LYS(BOC)-OH 1 G FMOC-N-ME-LYS(BOC)-OH 250 MG L-Lysine, N6-[(1,1-dimethylethoxy)carbonyl]-N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-N2-methyl- N-α-(9-Fluorenylmethoxycarbonyl)-N-α-methyl-N-ε-(t-butoxycarbonyl)-L-lysine (2S)-2-[9H-fluoren-9-ylmethoxycarbonyl(methyl)amino]-6-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid N6-Boc-N2-Fmoc-N2-methyl-L-lysine FM FM 197632-76-1 C27H34N2O6 amino acids