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71989-28-1,MFCD00037134
Catalog No.:AA00IC4R

71989-28-1 | Fmoc-L-Met-OH

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10g
98%
in stock  
$9.00   $7.00
- +
25g
98%
in stock  
$14.00   $10.00
- +
100g
98%
in stock  
$42.00   $29.00
- +
500g
98%
in stock  
$199.00   $139.00
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  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00IC4R
Chemical Name:
Fmoc-L-Met-OH
CAS Number:
71989-28-1
Molecular Formula:
C20H21NO4S
Molecular Weight:
371.4500
MDL Number:
MFCD00037134
SMILES:
CSCC[C@@H](C(=O)O)NC(=O)OCC1c2ccccc2c2c1cccc2 C20H21NO4S
Properties
Computed Properties
 
Complexity:
478  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
26  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
8  
XLogP3:
3.7  

Upstream Synthesis Route

[1]TetrahedronLetters,1993,vol.34,#9,p.1413-1414

[1]TetrahedronLetters,1993,vol.34,#9,p.1413-1414

[1]Patent:CN105622471,2016,A,.Locationinpatent:Paragraph0019;0020

[2]SyntheticCommunications,2009,vol.39,#11,p.2022-2031

[3]BioorganicandMedicinalChemistryLetters,2016,vol.26,#13,p.2980-2983

[1]Synlett,2011,#14,p.2013-2016

[1]EuropeanJournalofOrganicChemistry,2004,#21,p.4437-4441

Downstream Synthesis Route
29022-11-5    35737-15-6    71989-28-1    77128-73-5   
Hpa-OSu,Fmoc-D-Asp(t-Bu)-OH 
 
(R)-N-((S)-1-Carbamoyl-2-phenyl-ethyl)-3-{(S)-2-(S)-2-(2-{(S)-2-2-(4-hydroxy-phenyl)-acetylamino-4-methylsulfanyl-butyrylamino}-acetylamino)-3-(1H-indol-3-yl)-propionylamino-4-methylsulfanyl-butyrylamino}-N-methyl-succinamicacid 

[1]JournalofMedicinalChemistry,1997,vol.40,p.4302-4307

29022-11-5    35661-40-6    108-24-7    71989-28-1    198561-07-8   
Ac-Met(O2)-Asp-Phe-Gly-OH 

[1]OrganicLetters,2007,vol.9,p.2469-2472

C27H29ClNO5Pol 
  29022-11-5    35661-60-0    35661-40-6    71989-14-5    71989-28-1    462100-06-7   
Boc-11-amino-3,6,9-trioxaundecanoyl-Asp(OtBu)-Phe-Asp-(OtBu)-Leu-Asp(OtBu)-Met-Leu-Gly-Asp(OtBu)-Phe-Asp(OtBu)-Leu-Asp(OtBu)-Met-Leu-Gly-11-amino-3,6,9-trioxaundecanoicacid 

[1]BioorganicandMedicinalChemistry,2010,vol.18,p.6127-6133

35661-60-0    35661-39-3    71989-23-6    71989-26-9    71989-35-0    71989-28-1    132388-59-1    132327-80-1    143824-78-6   
Nα-(9-fluorenylmethyloxycarbonyl)-Nγ-2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl-L-arginine 
  198561-07-8   
H-(propargylglycyl)-QGTFTSDYSKYLDSRRAQDFVQWLMNTKRNRNNIA-NH2 

[1]JournalofPeptideScience,2011,vol.17,p.270-280

29022-11-5    68858-20-8    35661-60-0    35661-39-3    71989-31-6    71989-33-8    71989-14-5    71989-18-9    71989-35-0    71989-28-1    72040-64-3   
Fmoc-L-Arg(PG)-OH,PG=protectinggroup 
 
Fmoc-L-His(PG)-OH,PG=protectinggroup 
 
N-(biotinyl)-6-aminocaproyl-LSPLGEEMRDRARAHVDALRT-NH2 

[1]JournalofPeptideScience,2013,vol.19,p.220-226

Literature

Title: Adsorption induced enzyme denaturation: the role of polymer hydrophobicity in adsorption and denaturation of alpha-chymotrypsin on allyl glycidyl ether (AGE)-ethylene glycol dimethacrylate (EGDM) copolymers.

Journal: Langmuir : the ACS journal of surfaces and colloids 20100119

Title: Identification of homoserine lactone derivatives using the methionine functionalized solid phase synthesis by gas chromatography/mass spectrometry.

Journal: Archives of pharmacal research 20040101

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SDS
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