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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)-

Carbamic acid, (2-amino-2-oxoethyl)-, phenylmethyl ester

O=C(NCC(=O)N)OCc1ccccc1 Request for Quotation
Chemical Name: Carbamic acid, (2-amino-2-oxoethyl)-, phenylmethyl ester
CAS Number: 949-90-6
Product Number: AG005TLA(AGN-PC-0CJTZJ)
Synonyms:
MDL No:
Molecular Formula: C10H12N2O3
Molecular Weight: 208.2139

Identification/Properties

Properties
MP:
136-139 °C
BP:
447.1 °C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Stability:
Hygroscopic
Computed Properties
Molecular Weight:
208.217g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
208.085g/mol
Monoisotopic Mass:
208.085g/mol
Topological Polar Surface Area:
81.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
225
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Z-Gly-NH2, also known as Z-glycine amide, is a valuable chemical reagent widely used in chemical synthesis. It serves as a key building block in peptide synthesis, specifically in the formation of peptide bonds. Z-Gly-NH2 is often employed as a protecting group for the carboxylic acid functionality in amino acids, allowing for precise control over the sequence of peptide chain assembly. This compound facilitates the selective deprotection of the amino group during peptide bond formation, ensuring the desired structure and properties of the final peptide product. In addition, Z-Gly-NH2 is utilized in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals, highlighting its significance in the field of organic synthesis.