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7389-87-9,MFCD00012701
Catalog No.:AA005AIJ

7389-87-9 | (S)-Methyl 2-amino-3-(1h-imidazol-5-yl)propanoate 2hcl

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$6.00   $4.00
- +
5g
98%
in stock  
$7.00   $5.00
- +
10g
98%
in stock  
$9.00   $7.00
- +
25g
98%
in stock  
$21.00   $15.00
- +
100g
98%
in stock  
$51.00   $36.00
- +
500g
98%
in stock  
$193.00   $135.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA005AIJ
Chemical Name:
(S)-Methyl 2-amino-3-(1h-imidazol-5-yl)propanoate 2hcl
CAS Number:
7389-87-9
Molecular Formula:
C7H13Cl2N3O2
Molecular Weight:
242.1030
MDL Number:
MFCD00012701
SMILES:
COC(=O)[C@H](Cc1nc[nH]c1)N.Cl.Cl
Properties
Properties
 
Form:
Solid  
MP:
207 °C (dec.)(lit.)  
Refractive Index:
10 ° (C=2, H2O)  
Solubility:
100g/l  
Stability:
Hygroscopic  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
163  
Covalently-Bonded Unit Count:
3  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
4  
Isotope Atom Count:
0  
Rotatable Bond Count:
4  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  

Upstream Synthesis Route

[1]AdvancedSynthesisandCatalysis,2010,vol.352,#2-3,p.407-415

Downstream Synthesis Route
7389-87-9    103365-69-1   
1-methyl-(S)-Dio-His-OMe 

[1]JournalofMedicinalChemistry,1990,vol.33,p.2130-2137

[1]ActaChimicaHungarica,1992,vol.129,p.871-877

[1]TetrahedronAsymmetry,2008,vol.19,p.273-278

[2]Patent:US2009/93642,2009,A1.Locationinpatent:Page/Pagecolumn6;7

[1]AdvancedSynthesisandCatalysis,2010,vol.352,p.407-415

64017-81-8    7389-87-9   
L-carnosinemethylester 

[1]AdvancedSynthesisandCatalysis,2010,vol.352,p.407-415

Literature
Quotation Request
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SDS
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Tags:7389-87-9 Molecular Formula|7389-87-9 MDL|7389-87-9 SMILES|7389-87-9 (S)-Methyl 2-amino-3-(1h-imidazol-5-yl)propanoate 2hcl
Catalog No.: AA005AIJ
7389-87-9,MFCD00012701
7389-87-9 | (S)-Methyl 2-amino-3-(1h-imidazol-5-yl)propanoate 2hcl
Pack Size： 1g
Purity： 98%
in stock
$6.00 $4.00
Pack Size： 5g
Purity： 98%
in stock
$7.00 $5.00
Pack Size： 10g
Purity： 98%
in stock
$9.00 $7.00
Pack Size： 25g
Purity： 98%
in stock
$21.00 $15.00
Pack Size： 100g
Purity： 98%
in stock
$51.00 $36.00
Pack Size： 500g
Purity： 98%
in stock
$193.00 $135.00
Quantity
- +
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Technical Information
Catalog Number: AA005AIJ
Chemical Name: (S)-Methyl 2-amino-3-(1h-imidazol-5-yl)propanoate 2hcl
CAS Number: 7389-87-9
Molecular Formula: C7H13Cl2N3O2
Molecular Weight: 242.1030
MDL Number: MFCD00012701
SMILES: COC(=O)[C@H](Cc1nc[nH]c1)N.Cl.Cl
Properties
Form: Solid  
MP: 207 °C (dec.)(lit.)  
Refractive Index: 10 ° (C=2, H2O)  
Solubility: 100g/l  
Stability: Hygroscopic  
Storage: Inert atmosphere;2-8℃;  
Complexity: 163  
Covalently-Bonded Unit Count: 3  
Defined Atom Stereocenter Count: 1  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 14  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 4  
Isotope Atom Count: 0  
Rotatable Bond Count: 4  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
Upstream Synthesis Route
64017-81-8    7389-87-9    2140-53-6    1246364-63-5    1246364-64-6    305-84-0 

[1]AdvancedSynthesisandCatalysis,2010,vol.352,#2-3,p.407-415

Downstream Synthesis Route
7389-87-9    103365-69-1   
1-methyl-(S)-Dio-His-OMe 

[1]JournalofMedicinalChemistry,1990,vol.33,p.2130-2137

65-86-1    7389-87-9    78664-77-4 

[1]ActaChimicaHungarica,1992,vol.129,p.871-877

67-56-1    645-35-2    4467-54-3 

[1]TetrahedronAsymmetry,2008,vol.19,p.273-278

[2]Patent:US2009/93642,2009,A1.Locationinpatent:Page/Pagecolumn6;7

64017-81-8    7389-87-9    2140-53-6    1246364-63-5    1246364-64-6   
H-β-Ala-β-Ala-NH2 
  305-84-0 

[1]AdvancedSynthesisandCatalysis,2010,vol.352,p.407-415

64017-81-8    7389-87-9   
L-carnosinemethylester 

[1]AdvancedSynthesisandCatalysis,2010,vol.352,p.407-415

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