+1 858-523-8231
Login | Register
AA Blocks, Building Blocks, Catalysts, Inhibitors
Login | Register
Home PEG Linkers 557756-85-1
557756-85-1,MFCD06656472
Catalog No.:AA0038KJ

557756-85-1 | Fmoc-N-amido-PEG4-acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
98%
in stock  
$9.00   $6.00
- +
250mg
98%
in stock  
$13.00   $9.00
- +
1g
98%
in stock  
$19.00   $13.00
- +
5g
98%
in stock  
$86.00   $60.00
- +
10g
98%
in stock  
$156.00   $109.00
- +
25g
98%
in stock  
$315.00   $220.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA0038KJ
Chemical Name:
Fmoc-N-amido-PEG4-acid
CAS Number:
557756-85-1
Molecular Formula:
C26H33NO8
Molecular Weight:
487.5421
MDL Number:
MFCD06656472
SMILES:
OC(=O)CCOCCOCCOCCOCCNC(=O)OCC1c2ccccc2c2c1cccc2
Properties
Computed Properties
 
Complexity:
596  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
35  
Hydrogen Bond Acceptor Count:
8  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
18  
XLogP3:
2  

Downstream Synthesis Route

[1]Valverde,IbaiE.;Vomstein,Sandra;Mindt,ThomasL.[JournalofMedicinalChemistry,2016,vol.59,#8,p.3867-3877]

[1]Valverde,IbaiE.;Vomstein,Sandra;Mindt,ThomasL.[JournalofMedicinalChemistry,2016,vol.59,#8,p.3867-3877]

[1]Valverde,IbaiE.;Vomstein,Sandra;Mindt,ThomasL.[JournalofMedicinalChemistry,2016,vol.59,#8,p.3867-3877]

[1]Valverde,IbaiE.;Vomstein,Sandra;Mindt,ThomasL.[JournalofMedicinalChemistry,2016,vol.59,#8,p.3867-3877]

7423-55-4    68858-20-8   
(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-5-ureidopentanoicacid 
 
3-2-2-2-2-(9H-fluoren-9-ylmethoxycarbonylamino)ethoxyethoxyethoxyethoxypropanoicacid 
 
N-19-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)-17-oxo-4,7,10,13-tetraoxa-16-azanonadecan-1-oyl-L-valyl-N5-carbamoyl-L-ornithine 

[1]Patent:WO2020/84115,2020,A1.Locationinpatent:Page/Pagecolumn230

Literature

Title: Cai P, et al. Synthesis of C3-Alkylated Indoles on DNA via Indolyl Alcohol Formation Followed by Metal-FreeTransfer Hydrogenation. Org Lett. 2019 Aug 14.

Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Related Products of 557756-85-1
117106-20-4

117106-20-4

 146346-88-5

146346-88-5

 159610-93-2

159610-93-2

 1654740-73-4

1654740-73-4

 166108-71-0

166108-71-0

 204320-51-4

204320-51-4
Building Blocks
More >
Tags:557756-85-1 Molecular Formula|557756-85-1 MDL|557756-85-1 SMILES|557756-85-1 Fmoc-N-amido-PEG4-acid