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7752-82-1,MFCD00012341
Catalog No.:AA00330U

7752-82-1 | 2-Amino-5-bromopyrimidine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
97%
in stock  
$6.00   $4.00
- +
1g
97%
in stock  
$7.00   $5.00
- +
5g
98%
in stock  
$9.00   $6.00
- +
10g
98%
in stock  
$10.00   $7.00
- +
25g
97%
in stock  
$14.00   $10.00
- +
100g
97%
in stock  
$35.00   $25.00
- +
500g
97%
in stock  
$174.00   $122.00
- +
  • Technical Information
  • Properties
  • Literature
  • Application
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA00330U
Chemical Name:
2-Amino-5-bromopyrimidine
CAS Number:
7752-82-1
Molecular Formula:
C4H4BrN3
Molecular Weight:
173.9987
MDL Number:
MFCD00012341
SMILES:
Brc1cnc(nc1)N
NSC Number:
27269
Properties
Properties
 
BP:
340.743 °C at 760 mmHg  
Form:
Solid  
MP:
241-243 °C(lit.)  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
69.7  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
0  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
0.5  

Literature

Title: Synthesis of pyridine, pyrimidine and pyridinone C-nucleoside phosphoramidites for probing cytosine function in RNA.

Journal: The Journal of organic chemistry 20091106

Application
2-Amino-5-bromopyrimidine is utilized in various synthetic routes to produce pyridine, pyrimidine, and pyridinone C-nucleoside phosphoramidites, as well as 2-phthalimido-5-bromopyrimidine. It serves as an intermediate in the synthesis of sulfanilamides and amino acids containing the pyrimidine ring system, with the resulting products exhibiting potential antiviral activity. This compound's versatility in organic synthesis makes it a valuable building block for the preparation of pharmaceuticals and bioactive molecules targeting viral infections.
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SDS
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Tags:7752-82-1 Molecular Formula|7752-82-1 MDL|7752-82-1 SMILES|7752-82-1 2-Amino-5-bromopyrimidine
Catalog No.: AA00330U
7752-82-1,MFCD00012341
7752-82-1 | 2-Amino-5-bromopyrimidine
Pack Size： 250mg
Purity： 97%
in stock
$6.00 $4.00
Pack Size： 1g
Purity： 97%
in stock
$7.00 $5.00
Pack Size： 5g
Purity： 98%
in stock
$9.00 $6.00
Pack Size： 10g
Purity： 98%
in stock
$10.00 $7.00
Pack Size： 25g
Purity： 97%
in stock
$14.00 $10.00
Pack Size： 100g
Purity： 97%
in stock
$35.00 $25.00
Pack Size： 500g
Purity： 97%
in stock
$174.00 $122.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA00330U
Chemical Name: 2-Amino-5-bromopyrimidine
CAS Number: 7752-82-1
Molecular Formula: C4H4BrN3
Molecular Weight: 173.9987
MDL Number: MFCD00012341
SMILES: Brc1cnc(nc1)N
NSC Number: 27269
Properties
BP: 340.743 °C at 760 mmHg  
Form: Solid  
MP: 241-243 °C(lit.)  
Storage: Keep in dry area;Room Temperature;  
Complexity: 69.7  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 8  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 0  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 0.5  
Literature fold

Title: Synthesis of pyridine, pyrimidine and pyridinone C-nucleoside phosphoramidites for probing cytosine function in RNA.

Journal: The Journal of organic chemistry20091106

Application fold 
2-Amino-5-bromopyrimidine is utilized in various synthetic routes to produce pyridine, pyrimidine, and pyridinone C-nucleoside phosphoramidites, as well as 2-phthalimido-5-bromopyrimidine. It serves as an intermediate in the synthesis of sulfanilamides and amino acids containing the pyrimidine ring system, with the resulting products exhibiting potential antiviral activity. This compound's versatility in organic synthesis makes it a valuable building block for the preparation of pharmaceuticals and bioactive molecules targeting viral infections.
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