24250-84-8,MFCD00063062
Catalog No.:AA0033VR

24250-84-8 | 4-Bromo-L-Phenylalanine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
>98%(HPLC)
in stock  
$27.00   $19.00
- +
5g
95%
in stock  
$31.00   $22.00
- +
10g
95%
in stock  
$58.00   $41.00
- +
25g
95%
in stock  
$121.00   $85.00
- +
100g
95%
in stock  
$450.00   $315.00
- +
  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0033VR
Chemical Name:
4-Bromo-L-Phenylalanine
CAS Number:
24250-84-8
Molecular Formula:
C9H10BrNO2
Molecular Weight:
244.0852
MDL Number:
MFCD00063062
SMILES:
NC(C(=O)O)Cc1ccc(cc1)Br
Properties
Properties
 
BP:
368.4 °C at 760 mmHg  
Form:
Solid  
MP:
~265 °C (dec.)  
Storage:
Light sensitive;Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
179  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0  
Rotatable Bond Count:
3  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
-0.4  

Literature

Title: Macrocyclic β-sheet peptides that inhibit the aggregation of a tau-protein-derived hexapeptide.

Journal: Journal of the American Chemical Society 20110309

Title: The de novo engineering of pyrrolysyl-tRNA synthetase for genetic incorporation of L-phenylalanine and its derivatives.

Journal: Molecular bioSystems 20110301

Title: X-ray crystallographic structure of an artificial beta-sheet dimer.

Journal: Journal of the American Chemical Society 20100825

Title: Site-specific incorporation of 4-iodo-L-phenylalanine through opal suppression.

Journal: Journal of biochemistry 20100801

Title: Design of a bacterial host for site-specific incorporation of p-bromophenylalanine into recombinant proteins.

Journal: Journal of the American Chemical Society 20060913

Title: Neighbouring group processes in the deamination of protonated phenylalanine derivatives.

Journal: Organic & biomolecular chemistry 20051021

Title: Asymmetric synthesis of N-protected amino acids by the addition of organolithium carboxyl synthons to ROPHy/SOPHy-derived aldoximes and ketoximes.

Journal: Organic & biomolecular chemistry 20040121

Title: Biphenyls as potent vitronectin receptor antagonists. Part 2: biphenylalanine ureas.

Journal: Bioorganic & medicinal chemistry letters 20030324

Title: Unnatural amino acid mutagenesis of green fluorescent protein.

Journal: The Journal of organic chemistry 20030110

Title: 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: Journal of mass spectrometry : JMS 20020401

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SDS
Tags:24250-84-8 Molecular Formula|24250-84-8 MDL|24250-84-8 SMILES|24250-84-8 4-Bromo-L-Phenylalanine
Catalog No.: AA0033VR
24250-84-8,MFCD00063062
24250-84-8 | 4-Bromo-L-Phenylalanine
Pack Size: 1g
Purity: >98%(HPLC)
in stock
$27.00 $19.00
Pack Size: 5g
Purity: 95%
in stock
$31.00 $22.00
Pack Size: 10g
Purity: 95%
in stock
$58.00 $41.00
Pack Size: 25g
Purity: 95%
in stock
$121.00 $85.00
Pack Size: 100g
Purity: 95%
in stock
$450.00 $315.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0033VR
Chemical Name: 4-Bromo-L-Phenylalanine
CAS Number: 24250-84-8
Molecular Formula: C9H10BrNO2
Molecular Weight: 244.0852
MDL Number: MFCD00063062
SMILES: NC(C(=O)O)Cc1ccc(cc1)Br
Properties
BP: 368.4 °C at 760 mmHg  
Form: Solid  
MP: ~265 °C (dec.)  
Storage: Light sensitive;Keep in dry area;Room Temperature;  
Complexity: 179  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Isotope Atom Count: 0  
Rotatable Bond Count: 3  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: -0.4  
Literature fold

Title: Macrocyclic β-sheet peptides that inhibit the aggregation of a tau-protein-derived hexapeptide.

Journal: Journal of the American Chemical Society20110309

Title: The de novo engineering of pyrrolysyl-tRNA synthetase for genetic incorporation of L-phenylalanine and its derivatives.

Journal: Molecular bioSystems20110301

Title: X-ray crystallographic structure of an artificial beta-sheet dimer.

Journal: Journal of the American Chemical Society20100825

Title: Site-specific incorporation of 4-iodo-L-phenylalanine through opal suppression.

Journal: Journal of biochemistry20100801

Title: Design of a bacterial host for site-specific incorporation of p-bromophenylalanine into recombinant proteins.

Journal: Journal of the American Chemical Society20060913

Title: Neighbouring group processes in the deamination of protonated phenylalanine derivatives.

Journal: Organic & biomolecular chemistry20051021

Title: Asymmetric synthesis of N-protected amino acids by the addition of organolithium carboxyl synthons to ROPHy/SOPHy-derived aldoximes and ketoximes.

Journal: Organic & biomolecular chemistry20040121

Title: Biphenyls as potent vitronectin receptor antagonists. Part 2: biphenylalanine ureas.

Journal: Bioorganic & medicinal chemistry letters20030324

Title: Unnatural amino acid mutagenesis of green fluorescent protein.

Journal: The Journal of organic chemistry20030110

Title: 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: Journal of mass spectrometry : JMS20020401

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