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92954-90-0,MFCD00134890
Catalog No.:AA00IHBT

92954-90-0 | Fmoc-Tyr-OH

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$6.00   $4.00
- +
5g
98%
in stock  
$7.00   $5.00
- +
10g
98%
in stock  
$13.00   $9.00
- +
25g
98%
in stock  
$31.00   $22.00
- +
100g
98%
in stock  
$93.00   $65.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00IHBT
Chemical Name:
Fmoc-Tyr-OH
CAS Number:
92954-90-0
Molecular Formula:
C24H21NO5
Molecular Weight:
403.4272
MDL Number:
MFCD00134890
SMILES:
O=C(N[C@H](C(=O)O)Cc1ccc(cc1)O)OCC1c2ccccc2c2c1cccc2 C24H21NO5
Properties
Computed Properties
 
Complexity:
580  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
30  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0  
Rotatable Bond Count:
7  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
4.3  

Downstream Synthesis Route
CASUnavailable 
  29022-11-5   
CASUnavailable 
  1435263-70-9    92954-90-0    79990-15-1    175453-08-4    1435264-45-1 

[1]Petrov,RavilR.;Lee,YeonSun;Vardanyan,RubenS.;Liu,Lu;Ma,Shou-Wu;Davis,Peg;Lai,Josephine;Porreca,Frank;Vanderah,ToddW.;Hruby,VictorJ.[BioorganicandMedicinalChemistryLetters,2013,vol.23,#11,p.3434-3437]

CASUnavailable 
  1435263-70-9   
CASUnavailable 
  92954-90-0    71989-31-6    35737-15-6    175453-08-4    1435264-53-1 

[1]Petrov,RavilR.;Lee,YeonSun;Vardanyan,RubenS.;Liu,Lu;Ma,Shou-Wu;Davis,Peg;Lai,Josephine;Porreca,Frank;Vanderah,ToddW.;Hruby,VictorJ.[BioorganicandMedicinalChemistryLetters,2013,vol.23,#11,p.3434-3437]

21691-53-2    29022-11-5   
Fmoc-Arg(Pbf)-OH 
 
H-Asp-(tBu) 
 
N-Fmoc-Tyr-OH 
  18942-49-9    71989-31-6    71989-18-9    71989-23-6    132388-59-1    128270-60-0 

[1]CurrentPatentAssignee:CHEMICALBIOPHARMACEUTICALLABORATORIESOFPATRAS;CHEMICALBIOPHARMACEUTICALLABORATORIESOFPATRA-US9388212,2016,B2Locationinpatent:Page/Pagecolumn19;26

908846-88-8    27144-18-9    29022-11-5    112883-29-1    71989-14-5    71989-26-9    103213-32-7   
9-fluorenylmethoxycarbonyl-Nim-trityl-L-histidine 
 
(S)-1-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-methylpyrrolidine-2-carboxylicacid 
  76-05-1   
C61H75F2N15O13S2*C2HF3O2 

[1]Patent:WO2019/246349,2019,A1.Locationinpatent:Page/Pagecolumn149-150

908846-88-8    27144-18-9    29022-11-5   
N-(((9H-fluoren-9-yl)methoxy)carbonyl)-N-trityl-L-histidine 
  112883-29-1    71989-14-5    71989-26-9    103213-32-7   
(S)-1-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-methylpyrrolidine-2-carboxylicacid 
  76-05-1   
C61H75F2N15O13S2*C2HF3O2 

[1]Patent:WO2019/246387,2019,A1.Locationinpatent:Page/Pagecolumn91-93

[2]Patent:WO2019/246405,2019,A1.Locationinpatent:Page/Pagecolumn325-327

[3]Patent:WO2020/9805,2020,A2.Locationinpatent:Page/Pagecolumn104-106

Literature

Title: Coupling strategies for the synthesis of Peptide-oligonucleotide conjugates for patterned synthetic biomineralization.

Journal: Journal of nucleic acids 20110101

Title: Controlled release from modified amino acid hydrogels governed by molecular size or network dynamics.

Journal: Langmuir : the ACS journal of surfaces and colloids 20090901

Title: Quantitation of amino acids in plasma by high performance liquid chromatography: simultaneous deproteinization and derivatization with 9-fluorenylmethyloxycarbonyl chloride.

Journal: Journal of chromatography. A 20090821

Title: Design and synthesis of new N-(fluorenyl-9-methoxycarbonyl) (Fmoc)-dipeptides as anti-inflammatory agents.

Journal: European journal of medicinal chemistry 20090501

Title: Amino acid analysis by high-performance liquid chromatography after derivatization with 9-fluorenylmethyloxycarbonyl chloride Literature overview and further study.

Journal: Journal of chromatography. A 20090410

Title: Designed amino acid ATRP initiators for the synthesis of biohybrid materials.

Journal: Journal of the American Chemical Society 20080123

Title: Adsorption on molecularly imprinted polymers of structural analogues of a template. Single-component adsorption isotherm data.

Journal: Analytical chemistry 20051001

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Tags:92954-90-0 Molecular Formula|92954-90-0 MDL|92954-90-0 SMILES|92954-90-0 Fmoc-Tyr-OH
Catalog No.: AA00IHBT
92954-90-0,MFCD00134890
92954-90-0 | Fmoc-Tyr-OH
Pack Size： 1g
Purity： 98%
in stock
$6.00 $4.00
Pack Size： 5g
Purity： 98%
in stock
$7.00 $5.00
Pack Size： 10g
Purity： 98%
in stock
$13.00 $9.00
Pack Size： 25g
Purity： 98%
in stock
$31.00 $22.00
Pack Size： 100g
Purity： 98%
in stock
$93.00 $65.00
Quantity
- +
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Technical Information
Catalog Number: AA00IHBT
Chemical Name: Fmoc-Tyr-OH
CAS Number: 92954-90-0
Molecular Formula: C24H21NO5
Molecular Weight: 403.4272
MDL Number: MFCD00134890
SMILES: O=C(N[C@H](C(=O)O)Cc1ccc(cc1)O)OCC1c2ccccc2c2c1cccc2 C24H21NO5
Properties
Complexity: 580  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 30  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 3  
Isotope Atom Count: 0  
Rotatable Bond Count: 7  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 4.3  
Downstream Synthesis Route
CASUnavailable 
  29022-11-5   
CASUnavailable 
  1435263-70-9    92954-90-0    79990-15-1    175453-08-4    1435264-45-1 

[1]Petrov,RavilR.;Lee,YeonSun;Vardanyan,RubenS.;Liu,Lu;Ma,Shou-Wu;Davis,Peg;Lai,Josephine;Porreca,Frank;Vanderah,ToddW.;Hruby,VictorJ.[BioorganicandMedicinalChemistryLetters,2013,vol.23,#11,p.3434-3437]

CASUnavailable 
  1435263-70-9   
CASUnavailable 
  92954-90-0    71989-31-6    35737-15-6    175453-08-4    1435264-53-1 

[1]Petrov,RavilR.;Lee,YeonSun;Vardanyan,RubenS.;Liu,Lu;Ma,Shou-Wu;Davis,Peg;Lai,Josephine;Porreca,Frank;Vanderah,ToddW.;Hruby,VictorJ.[BioorganicandMedicinalChemistryLetters,2013,vol.23,#11,p.3434-3437]

21691-53-2    29022-11-5   
Fmoc-Arg(Pbf)-OH 
 
H-Asp-(tBu) 
 
N-Fmoc-Tyr-OH 
  18942-49-9    71989-31-6    71989-18-9    71989-23-6    132388-59-1    128270-60-0 

[1]CurrentPatentAssignee:CHEMICALBIOPHARMACEUTICALLABORATORIESOFPATRAS;CHEMICALBIOPHARMACEUTICALLABORATORIESOFPATRA-US9388212,2016,B2Locationinpatent:Page/Pagecolumn19;26

908846-88-8    27144-18-9    29022-11-5    112883-29-1    71989-14-5    71989-26-9    103213-32-7   
9-fluorenylmethoxycarbonyl-Nim-trityl-L-histidine 
 
(S)-1-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-methylpyrrolidine-2-carboxylicacid 
  76-05-1   
C61H75F2N15O13S2*C2HF3O2 

[1]Patent:WO2019/246349,2019,A1.Locationinpatent:Page/Pagecolumn149-150

908846-88-8    27144-18-9    29022-11-5   
N-(((9H-fluoren-9-yl)methoxy)carbonyl)-N-trityl-L-histidine 
  112883-29-1    71989-14-5    71989-26-9    103213-32-7   
(S)-1-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-methylpyrrolidine-2-carboxylicacid 
  76-05-1   
C61H75F2N15O13S2*C2HF3O2 

[1]Patent:WO2019/246387,2019,A1.Locationinpatent:Page/Pagecolumn91-93

[2]Patent:WO2019/246405,2019,A1.Locationinpatent:Page/Pagecolumn325-327

[3]Patent:WO2020/9805,2020,A2.Locationinpatent:Page/Pagecolumn104-106

Literature fold

Title: Coupling strategies for the synthesis of Peptide-oligonucleotide conjugates for patterned synthetic biomineralization.

Journal: Journal of nucleic acids20110101

Title: Controlled release from modified amino acid hydrogels governed by molecular size or network dynamics.

Journal: Langmuir : the ACS journal of surfaces and colloids20090901

Title: Quantitation of amino acids in plasma by high performance liquid chromatography: simultaneous deproteinization and derivatization with 9-fluorenylmethyloxycarbonyl chloride.

Journal: Journal of chromatography. A20090821

Title: Design and synthesis of new N-(fluorenyl-9-methoxycarbonyl) (Fmoc)-dipeptides as anti-inflammatory agents.

Journal: European journal of medicinal chemistry20090501

Title: Amino acid analysis by high-performance liquid chromatography after derivatization with 9-fluorenylmethyloxycarbonyl chloride Literature overview and further study.

Journal: Journal of chromatography. A20090410

Title: Designed amino acid ATRP initiators for the synthesis of biohybrid materials.

Journal: Journal of the American Chemical Society20080123

Title: Adsorption on molecularly imprinted polymers of structural analogues of a template. Single-component adsorption isotherm data.

Journal: Analytical chemistry20051001

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