Home Other Building Blocks 4-Bromo-L-Phenylalanine

4-Bromo-L-Phenylalanine

CAS No.:
24250-84-8
Catalog Number:
AG0033YJ
Molecular Formula:
C9H10BrNO2
Molecular Weight:
244.0852
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$23
- +
5g
98%
In Stock USA
United States
$62
- +
10g
98%
In Stock USA
United States
$94
- +
25g
98%
In Stock USA
United States
$182
- +
100g
98%
In Stock USA
United States
$500
- +
Product Description
Catalog Number:
AG0033YJ
Chemical Name:
4-Bromo-L-Phenylalanine
CAS Number:
24250-84-8
Molecular Formula:
C9H10BrNO2
Molecular Weight:
244.0852
MDL Number:
MFCD00063062
IUPAC Name:
(2S)-2-amino-3-(4-bromophenyl)propanoic acid
InChI:
InChI=1S/C9H10BrNO2/c10-7-3-1-6(2-4-7)5-8(11)9(12)13/h1-4,8H,5,11H2,(H,12,13)/t8-/m0/s1
InChI Key:
PEMUHKUIQHFMTH-QMMMGPOBSA-N
SMILES:
NC(C(=O)O)Cc1ccc(cc1)Br
Properties
Complexity:
179  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
242.989g/mol
Formal Charge:
0
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
244.088g/mol
Monoisotopic Mass:
242.989g/mol
Rotatable Bond Count:
3  
Topological Polar Surface Area:
63.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.4  
Literature
Title Journal
Macrocyclic β-sheet peptides that inhibit the aggregation of a tau-protein-derived hexapeptide. Journal of the American Chemical Society 20110309
The de novo engineering of pyrrolysyl-tRNA synthetase for genetic incorporation of L-phenylalanine and its derivatives. Molecular bioSystems 20110301
X-ray crystallographic structure of an artificial beta-sheet dimer. Journal of the American Chemical Society 20100825
Site-specific incorporation of 4-iodo-L-phenylalanine through opal suppression. Journal of biochemistry 20100801
Design of a bacterial host for site-specific incorporation of p-bromophenylalanine into recombinant proteins. Journal of the American Chemical Society 20060913
Neighbouring group processes in the deamination of protonated phenylalanine derivatives. Organic & biomolecular chemistry 20051021
Asymmetric synthesis of N-protected amino acids by the addition of organolithium carboxyl synthons to ROPHy/SOPHy-derived aldoximes and ketoximes. Organic & biomolecular chemistry 20040121
Biphenyls as potent vitronectin receptor antagonists. Part 2: biphenylalanine ureas. Bioorganic & medicinal chemistry letters 20030324
Unnatural amino acid mutagenesis of green fluorescent protein. The Journal of organic chemistry 20030110
Influence of a ring substituent on the tendency to form H(2)O adducts to Ag(+) complexes with phenylalanine analogues in an ion trap mass spectrometer. Journal of mass spectrometry : JMS 20020401
Properties