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116611-64-4,MFCD00190885
Catalog No.:AA000CSQ

116611-64-4 | Fmoc-His-OH

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
98%
in stock  
$7.00   $5.00
- +
1g
98%
in stock  
$9.00   $7.00
- +
5g
98%
in stock  
$29.00   $21.00
- +
10g
95%
in stock  
$42.00   $29.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA000CSQ
Chemical Name:
Fmoc-His-OH
CAS Number:
116611-64-4
Molecular Formula:
C21H19N3O4
Molecular Weight:
377.3933
MDL Number:
MFCD00190885
SMILES:
O=C(N[C@H](C(=O)O)Cc1c[nH]cn1)OCC1c2ccccc2c2c1cccc2
Properties
Computed Properties
 
Complexity:
550  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
28  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
7  
XLogP3:
2.8  

Literature

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

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SDS
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Tags:116611-64-4 Molecular Formula|116611-64-4 MDL|116611-64-4 SMILES|116611-64-4 Fmoc-His-OH
Catalog No.: AA000CSQ
116611-64-4,MFCD00190885
116611-64-4 | Fmoc-His-OH
Pack Size： 250mg
Purity： 98%
in stock
$7.00 $5.00
Pack Size： 1g
Purity： 98%
in stock
$9.00 $7.00
Pack Size： 5g
Purity： 98%
in stock
$29.00 $21.00
Pack Size： 10g
Purity： 95%
in stock
$42.00 $29.00
Quantity
- +
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Technical Information
Catalog Number: AA000CSQ
Chemical Name: Fmoc-His-OH
CAS Number: 116611-64-4
Molecular Formula: C21H19N3O4
Molecular Weight: 377.3933
MDL Number: MFCD00190885
SMILES: O=C(N[C@H](C(=O)O)Cc1c[nH]cn1)OCC1c2ccccc2c2c1cccc2
Properties
Complexity: 550  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 28  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 3  
Rotatable Bond Count: 7  
XLogP3: 2.8  
Literature fold

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

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