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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)-

2-Propenamide-2,3,3-d3

C(=C(C(=O)N)[2H])([2H])[2H] Request for Quotation
Chemical Name: 2-Propenamide-2,3,3-d3
CAS Number: 122775-19-3
Product Number: AG000JG1(AGN-PC-0PGNS1)
Synonyms:
MDL No:
Molecular Formula: C3H2D3NO
Molecular Weight: 74.0964

Identification/Properties

Computed Properties
Molecular Weight:
74.097g/mol
XLogP3:
-0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
74.056g/mol
Monoisotopic Mass:
74.056g/mol
Topological Polar Surface Area:
43.1A^2
Heavy Atom Count:
5
Formal Charge:
0
Complexity:
57.9
Isotope Atom Count:
3
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Acrylamide-d3 is a deuterated form of acrylamide, a commonly used chemical in various applications. In chemical synthesis, Acrylamide-d3 serves as a valuable tool for isotopic labeling. By replacing hydrogen atoms with deuterium atoms in acrylamide, it allows for the tracking and identification of specific molecules in complex chemical systems.The isotopic substitution of deuterium in acrylamide-d3 provides distinct advantages in chemical synthesis processes. One of the key benefits is the ability to differentiate between different reaction pathways or products through nuclear magnetic resonance (NMR) spectroscopy. This is crucial in elucidating reaction mechanisms and understanding the behavior of molecules in a reaction mixture.Additionally, the use of Acrylamide-d3 in chemical synthesis enables researchers to study the kinetics and thermodynamics of reactions more accurately. The isotopic labeling facilitates precise measurements of reaction rates, equilibrium constants, and isotope effects, leading to a deeper comprehension of the underlying chemical processes.Furthermore, Acrylamide-d3 can also be employed in the synthesis of other labeled compounds for various research applications. Its versatility and reliability make it an indispensable tool in the field of organic chemistry, allowing scientists to probe and manipulate molecular structures with precision and specificity.