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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)-

N-Acetyl-dl-Tryptophan

CC(=O)NC(C(=O)O)Cc1c[nH]c2c1cccc2 Request for Quotation
Chemical Name: N-Acetyl-dl-Tryptophan
CAS Number: 87-32-1
Product Number: AG003SOV(AGN-PC-0WAEF4)
Synonyms:
MDL No:
Molecular Formula: C13H14N2O3
Molecular Weight: 246.2619

Identification/Properties

Properties
MP:
204-206 °C (dec.)(lit.)
BP:
586.6°C at 760 mmHg
Storage:
Room Temperature;Light sensitive;Inert atmosphere;
Form:
Solid
Refractive Index:
1.6450 (estimate)
Computed Properties
Molecular Weight:
246.266g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
246.1g/mol
Monoisotopic Mass:
246.1g/mol
Topological Polar Surface Area:
82.2A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
332
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#:
N/A
Hazard Statements:
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


N-Acetyl-DL-tryptophan is a valuable compound widely used in chemical synthesis as a key building block for various processes. This versatile chemical is particularly utilized in the production of pharmaceuticals, agrochemicals, and specialty chemicals. In chemical synthesis, N-Acetyl-DL-tryptophan serves as a crucial intermediate in the creation of complex molecules, enabling the formation of new bonds and facilitating the development of novel compounds with diverse properties and applications. Its unique structure and reactivity make it an essential component in organic chemistry, allowing for the synthesis of a wide range of compounds with potential uses in various industries.