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5680-79-5,MFCD00012870
Catalog No.:AA0034WA

5680-79-5 | Glycine methyl ester hydrochloride

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Purity
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Price(USD)
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1g
98%
in stock  
$8.00   $6.00
- +
5g
98%
in stock  
$12.00   $8.00
- +
25g
98%
in stock  
$14.00   $10.00
- +
100g
98%
in stock  
$17.00   $12.00
- +
500g
98%
in stock  
$21.00   $15.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0034WA
Chemical Name:
Glycine methyl ester hydrochloride
CAS Number:
5680-79-5
Molecular Formula:
C3H8ClNO2
Molecular Weight:
125.5541
MDL Number:
MFCD00012870
SMILES:
COC(=O)CN.Cl
NSC Number:
9229
Properties
Properties
 
BP:
82.1 °C at 760 mmHg  
Form:
Solid  
MP:
175 °C (dec.)(lit.)  
Solubility:
>1000 g/L (20°C)  
Stability:
Hygroscopic  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
52.8  
Covalently-Bonded Unit Count:
2  
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
2  

Upstream Synthesis Route

[1]TetrahedronLetters,2010,vol.51,#31,p.4150-4152

[1]OrganicPreparationsandProceduresInternational,2002,vol.34,#1,p.87-94

[1]ArchivderPharmazie,2011,vol.344,#5,p.320-332

[1]OrganicandBiomolecularChemistry,2013,vol.11,#13,p.2198-2205

[2]PhotochemistryandPhotobiology,2005,vol.81,#6,p.1439-1446

[3]ArchivderPharmazie,1973,vol.306,#11,p.834-845

[4]JournaloftheAmericanChemicalSociety,1996,vol.118,#26,p.6105-6109

[1]HelveticaChimicaActa,1985,vol.68,p.135-143

Downstream Synthesis Route

[1]ChemischeBerichte,1970,vol.103,p.1655-1708

[1]JournalofgeneralchemistryoftheUSSR,1970,vol.40,p.202-213    ZhurnalObshcheiKhimii,1970,vol.40,p.223-235

[2]JournalofgeneralchemistryoftheUSSR,1970,vol.40,p.395-407    ZhurnalObshcheiKhimii,1970,vol.40,p.429-443

[1]AngewandteChemie-InternationalEdition,2019,vol.58,p.1208-1212    Angew.Chem.,2019,vol.131,p.1221-1225,5

[2]OrganicandBiomolecularChemistry,2013,vol.11,p.2198-2205

[3]PhotochemistryandPhotobiology,2005,vol.81,p.1439-1446

[4]ArchivderPharmazie,1973,vol.306,p.834-845

[5]JournaloftheAmericanChemicalSociety,1996,vol.118,p.6105-6109

[1]JournalofMedicinalChemistry,1981,vol.24,p.1119-1124

Literature

Title: Glycine enolates: the effect of formation of iminium ions to simple ketones on alpha-amino carbon acidity and a comparison with pyridoxal iminium ions.

Journal: Journal of the American Chemical Society 20080213

Title: New zinc(II)-based catalyst for asymmetric azomethine ylide cycloaddition reactions.

Journal: Organic letters 20061012

Title: Positive charges on lysine residues of the extrinsic 18 kDa protein are important to its electrostatic interaction with spinach photosystem II membranes.

Journal: Acta biochimica et biophysica Sinica 20051101

Title: Cu(I)-catalyzed highly exo-selective and enantioselective [3 + 2] cycloaddition of azomethine ylides with acrylates.

Journal: Organic letters 20050915

Title: Efficient microwave combinatorial parallel and nonparallel synthesis of N-alkylated glycine methyl esters as peptide building blocks.

Journal: Journal of combinatorial chemistry 20050101

Title: Identification of domains on the extrinsic 23 kDa protein possibly involved in electrostatic interaction with the extrinsic 33 kDa protein in spinach photosystem II.

Journal: European journal of biochemistry 20040301

Title: Sweetness and enzymatic activity of lysozyme.

Journal: Journal of agricultural and food chemistry 20011001

Title: Effect of modification of the carboxyl groups of the sialic acid binding lectin from bullfrog (Rana catesbeiana) oocyte on anti-tumor activity.

Journal: Biological & pharmaceutical bulletin 20010901

Title: Glycine enolates: the large effect of iminium ion formation on alpha-amino carbon acidity.

Journal: Journal of the American Chemical Society 20010815

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SDS
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Tags:5680-79-5 Molecular Formula|5680-79-5 MDL|5680-79-5 SMILES|5680-79-5 Glycine methyl ester hydrochloride
Catalog No.: AA0034WA
5680-79-5,MFCD00012870
5680-79-5 | Glycine methyl ester hydrochloride
Pack Size： 1g
Purity： 98%
in stock
$8.00 $6.00
Pack Size： 5g
Purity： 98%
in stock
$12.00 $8.00
Pack Size： 25g
Purity： 98%
in stock
$14.00 $10.00
Pack Size： 100g
Purity： 98%
in stock
$17.00 $12.00
Pack Size： 500g
Purity： 98%
in stock
$21.00 $15.00
Quantity
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Technical Information
Catalog Number: AA0034WA
Chemical Name: Glycine methyl ester hydrochloride
CAS Number: 5680-79-5
Molecular Formula: C3H8ClNO2
Molecular Weight: 125.5541
MDL Number: MFCD00012870
SMILES: COC(=O)CN.Cl
NSC Number: 9229
Properties
BP: 82.1 °C at 760 mmHg  
Form: Solid  
MP: 175 °C (dec.)(lit.)  
Solubility: >1000 g/L (20°C)  
Stability: Hygroscopic  
Storage: Inert atmosphere;Room Temperature;  
Complexity: 52.8  
Covalently-Bonded Unit Count: 2  
Heavy Atom Count: 7  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 2  
Upstream Synthesis Route
5680-79-5    1611-78-5    1193-62-0 

[1]TetrahedronLetters,2010,vol.51,#31,p.4150-4152

683-57-8    5680-79-5    4774-22-5 

[1]OrganicPreparationsandProceduresInternational,2002,vol.34,#1,p.87-94

5680-79-5    79-07-2    4774-22-5 

[1]ArchivderPharmazie,2011,vol.344,#5,p.320-332

5680-79-5    74-89-5    22356-89-4 

[1]OrganicandBiomolecularChemistry,2013,vol.11,#13,p.2198-2205

[2]PhotochemistryandPhotobiology,2005,vol.81,#6,p.1439-1446

[3]ArchivderPharmazie,1973,vol.306,#11,p.834-845

[4]JournaloftheAmericanChemicalSociety,1996,vol.118,#26,p.6105-6109

5680-79-5    124-40-3    22356-89-4 

[1]HelveticaChimicaActa,1985,vol.68,p.135-143

Downstream Synthesis Route
10068-52-7    5680-79-5    27414-80-8 

[1]ChemischeBerichte,1970,vol.103,p.1655-1708

5680-79-5    3392-08-3    16257-04-8 

[1]JournalofgeneralchemistryoftheUSSR,1970,vol.40,p.202-213    ZhurnalObshcheiKhimii,1970,vol.40,p.223-235

[2]JournalofgeneralchemistryoftheUSSR,1970,vol.40,p.395-407    ZhurnalObshcheiKhimii,1970,vol.40,p.429-443

5680-79-5    74-89-5    22356-89-4 

[1]AngewandteChemie-InternationalEdition,2019,vol.58,p.1208-1212    Angew.Chem.,2019,vol.131,p.1221-1225,5

[2]OrganicandBiomolecularChemistry,2013,vol.11,p.2198-2205

[3]PhotochemistryandPhotobiology,2005,vol.81,p.1439-1446

[4]ArchivderPharmazie,1973,vol.306,p.834-845

[5]JournaloftheAmericanChemicalSociety,1996,vol.118,p.6105-6109

5680-79-5    5241-66-7    70668-86-9 

[1]JournalofMedicinalChemistry,1981,vol.24,p.1119-1124

Literature fold

Title: Glycine enolates: the effect of formation of iminium ions to simple ketones on alpha-amino carbon acidity and a comparison with pyridoxal iminium ions.

Journal: Journal of the American Chemical Society20080213

Title: New zinc(II)-based catalyst for asymmetric azomethine ylide cycloaddition reactions.

Journal: Organic letters20061012

Title: Positive charges on lysine residues of the extrinsic 18 kDa protein are important to its electrostatic interaction with spinach photosystem II membranes.

Journal: Acta biochimica et biophysica Sinica20051101

Title: Cu(I)-catalyzed highly exo-selective and enantioselective [3 + 2] cycloaddition of azomethine ylides with acrylates.

Journal: Organic letters20050915

Title: Efficient microwave combinatorial parallel and nonparallel synthesis of N-alkylated glycine methyl esters as peptide building blocks.

Journal: Journal of combinatorial chemistry20050101

Title: Identification of domains on the extrinsic 23 kDa protein possibly involved in electrostatic interaction with the extrinsic 33 kDa protein in spinach photosystem II.

Journal: European journal of biochemistry20040301

Title: Sweetness and enzymatic activity of lysozyme.

Journal: Journal of agricultural and food chemistry20011001

Title: Effect of modification of the carboxyl groups of the sialic acid binding lectin from bullfrog (Rana catesbeiana) oocyte on anti-tumor activity.

Journal: Biological & pharmaceutical bulletin20010901

Title: Glycine enolates: the large effect of iminium ion formation on alpha-amino carbon acidity.

Journal: Journal of the American Chemical Society20010815

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