1. Home
  2. Glycine, L-alanyl-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Glycine, L-alanyl-

CC(C(=O)NCC(=O)O)N Request for Quotation
Chemical Name: Glycine, L-alanyl-
CAS Number: 1188-01-8
Product Number: AG003PTC(AGN-PC-0NZOQT)
Synonyms:
MDL No:
Molecular Formula: C5H10N2O3
Molecular Weight: 146.1445

Identification/Properties

Properties
MP:
225 °C
BP:
265.74°C (rough estimate)
Storage:
-10 ℃;
Form:
Solid
Refractive Index:
1.4954 (estimate)
Computed Properties
Molecular Weight:
146.146g/mol
XLogP3:
-3.7
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
146.069g/mol
Monoisotopic Mass:
146.069g/mol
Topological Polar Surface Area:
92.4A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
146
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Glycine, alanyl- is a key component in chemical synthesis processes, utilized for its versatility and reactivity in various applications. This compound serves as a crucial building block for the creation of peptides and proteins through solid-phase synthesis methods. Its strategic incorporation in peptide synthesis allows for the formation of specific peptide bonds, crucial for the development of bioactive compounds and pharmaceuticals. Additionally, Glycine, alanyl- is employed in the production of custom amino acid derivatives, enabling the customization of molecular structures for research and industrial purposes. Its role in chemical synthesis extends to the creation of complex molecules, providing researchers with a valuable tool for designing and developing innovative materials and compounds.