+1 858-523-8231
Login | Register
menu
AA Blocks, Building Blocks, Catalysts, Inhibitors
Login | Register
1155-64-2,MFCD00002638
Catalog No.:AA003SLE

1155-64-2 | H-Lys(Z)-OH

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$6.00   $4.00
- +
10g
98%
in stock  
$8.00   $6.00
- +
100g
98%
in stock  
$32.00   $22.00
- +
500g
98%
in stock  
$152.00   $107.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA003SLE
Chemical Name:
H-Lys(Z)-OH
CAS Number:
1155-64-2
Molecular Formula:
C14H20N2O4
Molecular Weight:
280.3196
MDL Number:
MFCD00002638
SMILES:
O=C(OCc1ccccc1)NCCCC[C@@H](C(=O)O)N
Properties
Properties
 
BP:
499.6 °C at 760 mmHg  
Form:
Solid  
MP:
250-260 °C  
Refractive Index:
16 ° (C=1.6, 2mol/L HCl)  
Storage:
Room Temperature;  

Computed Properties
 
Complexity:
304  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
20  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0  
Rotatable Bond Count:
9  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-1.1  

Upstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,1952,vol.74,p.2002

[1]Patent:WO2017/89890,2017,A1,.Locationinpatent:Page/Pagecolumn117

[2]Chemistry-AEuropeanJournal,2014,vol.20,#26,p.8116-8128

[3]Tetrahedron,2014,vol.70,#34,p.5197-5206

[1]BulletinoftheChemicalSocietyofJapan,1989,vol.62,#10,p.3103-3108

[1]IndianJournalofChemistry,SectionB:OrganicChemistryIncludingMedicinalChemistry,1986,vol.25,p.230-232

[2]Tetrahedron,2001,vol.57,#43,p.9033-9043

[3]OrganicSyntheses,1985,vol.63,p.160-160

[4]JournalofChemicalResearch,Miniprint,1991,#5,p.914-934

[5]JournaloftheChemicalSociety-PerkinTransactions1,1998,#2,p.359-365

[6]Patent:WO2004/50084,2004,A2,.Locationinpatent:Page/Pagecolumn61;62

[7]ProteinandPeptideLetters,2010,vol.17,#7,p.847-853

[8]Patent:US2018/311342,2018,A1,.Locationinpatent:Paragraph1458-1460

[1]Patent:US4432971,1984,A,

Downstream Synthesis Route

[1]Patent:WO2006/47703,2006,A2.Locationinpatent:Page/Pagecolumn13-14

[2]JournaloftheChemicalSociety,1950,p.3222,3225

[3]Patent:US2716647,1952,

[4]JournalofPolymerScience,PartA:PolymerChemistry,2012,vol.50,p.2527-2532

[1]Locationinpatent:experimentalpartZhou,Yinjian;Zhao,Ming;Wu,Yingting;Li,Chunyu;Wu,Jianhui;Zheng,Meiqing;Peng,Li;Peng,Shiqi[BioorganicandMedicinalChemistry,2010,vol.18,#6,p.2165-2172]

[2]Slotin,L.A.etal.[CanadianJournalofChemistry,1977,vol.55,p.4257-4266]

[3]GRIMM;GRASSMANN[Hoppe-Seyler'sZeitschriftfurPhysiologischeChemie,1964,vol.337,p.161-171]

[4]Coggins,J.etal.[CanadianJournalofChemistry,1970,vol.48,p.385-387]

[5]Hartter[Hoppe-Seyler'sZeitschriftfurPhysiologischeChemie,1977,vol.358,#3,p.331-337]

[6]Peyman,Anusch;Wehner,Volkmar;Knolle,Jochen;Stilz,HansUlrich;Breipohl,Gerhard;Scheunemann,Karl-Heinz;Carniato,Denis;Ruxer,Jean-Marie;Gourvest,Jean-Francois;Gadek,ThomasR.;Bodary,Sarah[BioorganicandMedicinalChemistryLetters,2000,vol.10,#2,p.179-182]

[1]BulletinoftheChemicalSocietyofJapan,1976,vol.49,p.719-723

[1]Cai,Hongliang;Guengerich,F.Peter[JournaloftheAmericanChemicalSociety,1999,vol.121,#50,p.11656-11663]

[2]Moore;Rydon;Smithers[JournaloftheChemicalSociety.PerkintransactionsI,1966,vol.24,p.2349-2359]

[1]Vogler,K.etal.[HelveticaChimicaActa,1964,vol.47,p.526-544]

[2]Sakai;Kawai;Kamishohara;Odagawa;Suzuki;Uchida;Kawasaki;Tsuruo;Otake[JournalofAntibiotics,1995,vol.48,#6,p.504-508]

[3]CurrentPatentAssignee:THEWILLIAMMYARBROUGHFOUNDATION;THEWILLIAMMYARBROUGHFOUND-WO2014/18874,2014,A1Locationinpatent:Paragraph0050

[4]CurrentPatentAssignee:THEWILLIAMMYARBROUGHFOUNDATION-US2017/37000,2017,A1Locationinpatent:Paragraph0048

Literature

Title: Wide-range protein photo-crosslinking achieved by a genetically encoded N(ε)-(benzyloxycarbonyl)lysine derivative with a diazirinyl moiety.

Journal: Molecular bioSystems 20120401

Title: Multistep engineering of pyrrolysyl-tRNA synthetase to genetically encode N(epsilon)-(o-azidobenzyloxycarbonyl) lysine for site-specific protein modification.

Journal: Chemistry & biology 20081124

Title: Adding l-lysine derivatives to the genetic code of mammalian cells with engineered pyrrolysyl-tRNA synthetases.

Journal: Biochemical and biophysical research communications 20080711

Title: Novel amphiphilic poly(epsilon-caprolactone)-g-poly(L-lysine) degradable copolymers.

Journal: Biomacromolecules 20070801

Title: Synthesis of Nepsilon-protected-L-lysine and gamma-benzyl-L-glutamate N-carboxyanhydrides (NCA) by carbamoylation and nitrosation.

Journal: Amino acids 20041001

Title: Formation of a two-dimensionally well-ordered monolayer of a peptide oligomer by a simple spin-coating process.

Journal: Langmuir : the ACS journal of surfaces and colloids 20040203

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
Submit
SDS
Related Products of 1155-64-2
101250-90-2

101250-90-2

 1158-35-6

1158-35-6

 1195256-01-9

1195256-01-9

 1259278-10-8

1259278-10-8

 130312-10-6

130312-10-6

 130368-99-9

130368-99-9
Building Blocks
More >
Tags:1155-64-2 Molecular Formula|1155-64-2 MDL|1155-64-2 SMILES|1155-64-2 H-Lys(Z)-OH
Catalog No.: AA003SLE
1155-64-2,MFCD00002638
1155-64-2 | H-Lys(Z)-OH
Pack Size： 5g
Purity： 98%
in stock
$6.00 $4.00
Pack Size： 10g
Purity： 98%
in stock
$8.00 $6.00
Pack Size： 100g
Purity： 98%
in stock
$32.00 $22.00
Pack Size： 500g
Purity： 98%
in stock
$152.00 $107.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA003SLE
Chemical Name: H-Lys(Z)-OH
CAS Number: 1155-64-2
Molecular Formula: C14H20N2O4
Molecular Weight: 280.3196
MDL Number: MFCD00002638
SMILES: O=C(OCc1ccccc1)NCCCC[C@@H](C(=O)O)N
Properties
BP: 499.6 °C at 760 mmHg  
Form: Solid  
MP: 250-260 °C  
Refractive Index: 16 ° (C=1.6, 2mol/L HCl)  
Storage: Room Temperature;  
Complexity: 304  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 20  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 3  
Isotope Atom Count: 0  
Rotatable Bond Count: 9  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -1.1  
Upstream Synthesis Route
1155-64-2    576-19-2 

[1]JournaloftheAmericanChemicalSociety,1952,vol.74,p.2002

1155-64-2    501-53-1    405-39-0 

[1]Patent:WO2017/89890,2017,A1,.Locationinpatent:Page/Pagecolumn117

[2]Chemistry-AEuropeanJournal,2014,vol.20,#26,p.8116-8128

[3]Tetrahedron,2014,vol.70,#34,p.5197-5206

657-27-2    405-39-0    1155-64-2 

[1]BulletinoftheChemicalSocietyofJapan,1989,vol.62,#10,p.3103-3108

24424-99-5    1155-64-2    2389-45-9 

[1]IndianJournalofChemistry,SectionB:OrganicChemistryIncludingMedicinalChemistry,1986,vol.25,p.230-232

[2]Tetrahedron,2001,vol.57,#43,p.9033-9043

[3]OrganicSyntheses,1985,vol.63,p.160-160

[4]JournalofChemicalResearch,Miniprint,1991,#5,p.914-934

[5]JournaloftheChemicalSociety-PerkinTransactions1,1998,#2,p.359-365

[6]Patent:WO2004/50084,2004,A2,.Locationinpatent:Page/Pagecolumn61;62

[7]ProteinandPeptideLetters,2010,vol.17,#7,p.847-853

[8]Patent:US2018/311342,2018,A1,.Locationinpatent:Paragraph1458-1460

1155-64-2    58632-95-4    2389-45-9 

[1]Patent:US4432971,1984,A,

Downstream Synthesis Route
1155-64-2    1676-86-4 

[1]Patent:WO2006/47703,2006,A2.Locationinpatent:Page/Pagecolumn13-14

[2]JournaloftheChemicalSociety,1950,p.3222,3225

[3]Patent:US2716647,1952,

[4]JournalofPolymerScience,PartA:PolymerChemistry,2012,vol.50,p.2527-2532

67-56-1    1155-64-2    24498-31-5 

[1]Locationinpatent:experimentalpartZhou,Yinjian;Zhao,Ming;Wu,Yingting;Li,Chunyu;Wu,Jianhui;Zheng,Meiqing;Peng,Li;Peng,Shiqi[BioorganicandMedicinalChemistry,2010,vol.18,#6,p.2165-2172]

[2]Slotin,L.A.etal.[CanadianJournalofChemistry,1977,vol.55,p.4257-4266]

[3]GRIMM;GRASSMANN[Hoppe-Seyler'sZeitschriftfurPhysiologischeChemie,1964,vol.337,p.161-171]

[4]Coggins,J.etal.[CanadianJournalofChemistry,1970,vol.48,p.385-387]

[5]Hartter[Hoppe-Seyler'sZeitschriftfurPhysiologischeChemie,1977,vol.358,#3,p.331-337]

[6]Peyman,Anusch;Wehner,Volkmar;Knolle,Jochen;Stilz,HansUlrich;Breipohl,Gerhard;Scheunemann,Karl-Heinz;Carniato,Denis;Ruxer,Jean-Marie;Gourvest,Jean-Francois;Gadek,ThomasR.;Bodary,Sarah[BioorganicandMedicinalChemistryLetters,2000,vol.10,#2,p.179-182]

143-07-7    1155-64-2    59409-41-5 

[1]BulletinoftheChemicalSocietyofJapan,1976,vol.49,p.719-723

64-18-6    1155-64-2    53917-47-8 

[1]Cai,Hongliang;Guengerich,F.Peter[JournaloftheAmericanChemicalSociety,1999,vol.121,#50,p.11656-11663]

[2]Moore;Rydon;Smithers[JournaloftheChemicalSociety.PerkintransactionsI,1966,vol.24,p.2349-2359]

112-16-3    1155-64-2    106383-96-4 

[1]Vogler,K.etal.[HelveticaChimicaActa,1964,vol.47,p.526-544]

[2]Sakai;Kawai;Kamishohara;Odagawa;Suzuki;Uchida;Kawasaki;Tsuruo;Otake[JournalofAntibiotics,1995,vol.48,#6,p.504-508]

[3]CurrentPatentAssignee:THEWILLIAMMYARBROUGHFOUNDATION;THEWILLIAMMYARBROUGHFOUND-WO2014/18874,2014,A1Locationinpatent:Paragraph0050

[4]CurrentPatentAssignee:THEWILLIAMMYARBROUGHFOUNDATION-US2017/37000,2017,A1Locationinpatent:Paragraph0048

Literature fold

Title: Wide-range protein photo-crosslinking achieved by a genetically encoded N(ε)-(benzyloxycarbonyl)lysine derivative with a diazirinyl moiety.

Journal: Molecular bioSystems20120401

Title: Multistep engineering of pyrrolysyl-tRNA synthetase to genetically encode N(epsilon)-(o-azidobenzyloxycarbonyl) lysine for site-specific protein modification.

Journal: Chemistry & biology20081124

Title: Adding l-lysine derivatives to the genetic code of mammalian cells with engineered pyrrolysyl-tRNA synthetases.

Journal: Biochemical and biophysical research communications20080711

Title: Novel amphiphilic poly(epsilon-caprolactone)-g-poly(L-lysine) degradable copolymers.

Journal: Biomacromolecules20070801

Title: Synthesis of Nepsilon-protected-L-lysine and gamma-benzyl-L-glutamate N-carboxyanhydrides (NCA) by carbamoylation and nitrosation.

Journal: Amino acids20041001

Title: Formation of a two-dimensionally well-ordered monolayer of a peptide oligomer by a simple spin-coating process.

Journal: Langmuir : the ACS journal of surfaces and colloids20040203

Related Products of of 1155-64-2
101250-90-2
101250-90-2
1158-35-6
1158-35-6
1195256-01-9
1195256-01-9
1259278-10-8
1259278-10-8
130312-10-6
130312-10-6
130368-99-9
130368-99-9
Building Blocks More >
7689-50-1
7689-50-1
N-Benzylglycine, HCl
AA003SP0 | MFCD00156934
3589-41-1
3589-41-1
N-Carbobenzoxyaminoacetonitrile
AA003SSS | MFCD00033175
381670-28-6
381670-28-6
Ethyl (2-methyl-3-nitrophenyl)carbamate
AA003SWD | MFCD00059819
14267-17-5
14267-17-5
Bis(diethyldithiocarbamato)nickel
AA003T06 | MFCD00137706
85952-29-0
85952-29-0
N-Methyl-1-(4-nitrophenyl)methanesulfonamide
AA003T44 | MFCD00277775
6006-95-7
6006-95-7
N-Pentadecylcyclohexane
AA003T7U | MFCD00058952
93204-36-5
93204-36-5
Z-D-Serine methyl ester
AA003TBN | MFCD00799501
635-26-7
635-26-7
O-Tolylhydrazine, HCl
AA003TFJ | MFCD00012925
355-02-2
355-02-2
PERFLUORO(METHYLCYCLOHEXANE)
AA003TJX | MFCD00001468
89885-26-7
89885-26-7
Benzene, (trimethoxysilyl)-, homopolymer
AA01X3QI | MFCD00025689
Submit
© 2017 AA BLOCKS, INC. All rights reserved.