INDOLE-3-ACETYL-DL-ASPARTIC ACID

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Names

[ CAS No. ]:
32449-99-3

[ Name ]:
INDOLE-3-ACETYL-DL-ASPARTIC ACID

[Synonym ]:
N-(3-Indoleacetyl)-DL-aspartic acid
Aspartic acid,N-(3-indolylacetyl)
indole-3-acetyl-N-aspartic acid
Indole-3-acetyl-L-aspatic acid
N-indol-3-ylacetyl-DL-aspartic acid
MFCD00050396
Indol-3-acetylaspartic acid
Indole-3-acetyl-D,L-aspartic acid
N-Indol-3-ylacetyl-DL-asparaginsaeure
N-(3-Indolylacetyl)-DL-aspartic acid

Chemical & Physical Properties

[ Density]:
1.478g/cm3

[ Boiling Point ]:
641.7ºC at 760mmHg

[ Melting Point ]:
198ºC (dec.)(lit.)

[ Molecular Formula ]:
C14H14N2O5

[ Molecular Weight ]:
290.27100

[ Flash Point ]:
341.9ºC

[ Exact Mass ]:
290.09000

[ PSA ]:
119.49000

[ LogP ]:
1.14540

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933990090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 3-Indoleacetic acid
  • dibenzyl 2-aminosuccinate
  • Dicyclohexylcarbodiimide

DownStream

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

The Role of Amino Acid Permeases and Tryptophan Biosynthesis in Cryptococcus neoformans Survival.

PLoS ONE 10 , e0132369, (2015)

Metabolic diversity is an important factor during microbial adaptation to different environments. Among metabolic processes, amino acid biosynthesis has been demonstrated to be relevant for survival f...

Spectroscopic, kinetic, and mechanistic study of a new mode of coordination of indole derivatives to platinum(II) and palladium(II) ions in complexes.

Inorg. Chem. 39 , 5004, (2000)

Binding of tryptophan residue to intrinsic metal ions in proteins is unknown, and very little is known about the coordinating abilities of indole. Indole-3-acetamide displaces the solvent ligands from...


More Articles

Related Compounds

  • Indol-3-ylacetylaspartic acid
  • INDOLE-3-ACETYL-DL-TRYPTOPHAN
  • dimethyl (3S)-2-acetyl-3-aminobutanedioate,1H-indole
  • N-acetyl-DL-aspartic acid, compound with L-arginine (1:2)
  • N-Acetyl-DL-aspartic acid
  • N-[(2,4,5-trichloro-phenoxy)-acetyl]-DL-aspartic acid
  • 3-ethyl-5H,6H,7H,8H-imidazo[1,5-a]pyrazine-1-carboxylic acid
  • 4-[[2-(4-fluorophenyl)oxazol-4-yl]methoxy]-3-(hydroxymethyl)benzaldehyde
  • 2'-Fluoro-3'-methoxy-[1,1'-biphenyl]-4-amine
  • methyl 5H,6H,7H,8H-imidazo[1,2-a]pyrazine-3-carboxylate
  • Methyl 3-(trifluoromethyl)benzenesulfonate
  • 1-[(E)-2-(4-bromophenyl)vinyl]sulfonyl-3-methyl-2-phenyl-imidazolidin-4-one
  • 2-(2-Iodo-pyrimidin-4-yl)-1-methyl-4-oxo-1,4,6,7-tetrahydro-pyrrolo[3,2-c]pyridine-5-carboxylic acid tert-butyl ester
  • 1-trityl-1H-pyrazolo[3,4-b]pyridine-4-carbothioamide
  • 3-[[[(4-chlorophenyl)methyl-methyl-sulfamoyl]amino]methyl]-1-propyl-pyrrole
  • Methyl 6-[(2-aminoethyl)amino]pyridine-3-carboxylate
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