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5680-80-8,MFCD00063680
Catalog No.:AA003519

5680-80-8 | L-Serine methyl ester, HCl

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Purity
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5g
97%
in stock  
$11.00   $8.00
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10g
97%
in stock  
$13.00   $9.00
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25g
97%
in stock  
$16.00   $11.00
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100g
97%
in stock  
$50.00   $35.00
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500g
97%
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$83.00   $58.00
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  • Technical Information
  • Properties
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA003519
Chemical Name:
L-Serine methyl ester, HCl
CAS Number:
5680-80-8
Molecular Formula:
C4H10ClNO3
Molecular Weight:
155.5801
MDL Number:
MFCD00063680
SMILES:
COC(=O)C(CO)N.Cl
Properties
Properties
 
BP:
234.7°C at 760 mmHg  
Form:
Solid  
MP:
163 °C (dec.);(lit.);  
Stability:
Moisture Sensitive  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
83.4  
Covalently-Bonded Unit Count:
2  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
3  

Literature

Title: Acylated serine derivatives: a unique class of arthropod pheromones of the Australian redback spider, Latrodectus hasselti.

Journal: Angewandte Chemie (International ed. in English) 20100308

Title: Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Journal: Nature chemical biology 20090101

Title: Theoretical evidence for pyramidalized bicyclic serine enolates in highly diastereoselective alkylations.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20070101

Title: Aziridinium from N,N-dibenzyl serine methyl ester: synthesis of enantiomerically pure beta-amino and alpha,beta-diamino esters.

Journal: Organic letters 20060511

Title: Selective inhibition of divergent seryl-tRNA synthetases by serine analogues.

Journal: FEBS letters 20050815

Title: The novel and efficient direct synthesis of N,O-acetal compounds using a hypervalent iodine(III) reagent: an improved synthetic method for a key intermediate of discorhabdins.

Journal: Chemical communications (Cambridge, England) 20050407

Title: Contribution of the anomeric effect to the solution and crystal structure of [1S,2S,6S,7s]-1,6-diaza-4,9-dioxa-2,7-dimethoxycarbonylbicyclo[4.4.1]undecane, a condensation product of L-serine methyl ester with formaldehyde.

Journal: Carbohydrate research 20010115

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Tags:5680-80-8 Molecular Formula|5680-80-8 MDL|5680-80-8 SMILES|5680-80-8 L-Serine methyl ester, HCl