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2280-01-5 molecular structure
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(2R)-2-acetamido-3-(1H-indol-3-yl)propanoic acid

ChemBase ID: 102099
Molecular Formular: C13H14N2O3
Molecular Mass: 246.26186
Monoisotopic Mass: 246.10044232
SMILES and InChIs

SMILES:
CC(=O)N[C@H](Cc1c[nH]c2c1cccc2)C(=O)O
Canonical SMILES:
CC(=O)N[C@@H](C(=O)O)Cc1c[nH]c2c1cccc2
InChI:
InChI=1S/C13H14N2O3/c1-8(16)15-12(13(17)18)6-9-7-14-11-5-3-2-4-10(9)11/h2-5,7,12,14H,6H2,1H3,(H,15,16)(H,17,18)/t12-/m1/s1
InChIKey:
DZTHIGRZJZPRDV-GFCCVEGCSA-N

Cite this record

CBID:102099 http://www.chembase.cn/molecule-102099.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
(2R)-2-acetamido-3-(1H-indol-3-yl)propanoic acid
IUPAC Traditional name
N-acetyl-D-tryptophan
Synonyms
N-ACETYL-D-TRYPTOPHAN
N-Acetyl-D-tryptophan
CAS Number
2280-01-5
EC Number
218-912-4
MDL Number
MFCD00065021
PubChem SID
24891045
162089070
PubChem CID
439917

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
PubChem 439917 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 4.1183767  H Acceptors
H Donor LogD (pH = 5.5) -0.40099344 
LogD (pH = 7.4) -2.0920737  Log P 0.99522364 
Molar Refractivity 65.6466 cm3 Polarizability 26.452345 Å3
Polar Surface Area 82.19 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Safety Information Product Information Bioassay(PubChem)
Storage Condition
0°C, Protect from light expand Show data source
MSDS Link
Download expand Show data source
German water hazard class
3 expand Show data source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand Show data source
Storage Temperature
-20°C expand Show data source
Purity
95+% expand Show data source
Certificate of Analysis
Download expand Show data source

DETAILS

DETAILS

MP Biomedicals MP Biomedicals

REFERENCES

REFERENCES

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PATENTS

PATENTS

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INTERNET

INTERNET

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