Home > Compound List > Compound details
2872-52-8 molecular structure
click picture or here to close

2-[ethyl({4-[2-(4-nitrophenyl)diazen-1-yl]phenyl})amino]ethan-1-ol

ChemBase ID: 139051
Molecular Formular: C16H18N4O3
Molecular Mass: 314.33912
Monoisotopic Mass: 314.13789046
SMILES and InChIs

SMILES:
CCN(CCO)c1ccc(cc1)/N=N/c1ccc(cc1)[N+](=O)[O-]
Canonical SMILES:
OCCN(c1ccc(cc1)/N=N/c1ccc(cc1)[N+](=O)[O-])CC
InChI:
InChI=1S/C16H18N4O3/c1-2-19(11-12-21)15-7-3-13(4-8-15)17-18-14-5-9-16(10-6-14)20(22)23/h3-10,21H,2,11-12H2,1H3
InChIKey:
FOQABOMYTOFLPZ-UHFFFAOYSA-N

Cite this record

CBID:139051 http://www.chembase.cn/molecule-139051.html

Collapse All Expand All

NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
2-[ethyl({4-[2-(4-nitrophenyl)diazen-1-yl]phenyl})amino]ethan-1-ol
IUPAC Traditional name
2-[ethyl({4-[2-(4-nitrophenyl)diazen-1-yl]phenyl})amino]ethanol
Synonyms
N-Ethyl-N-(2-hydroxyethyl)-4-(4-nitrophenylazo)aniline
Disperse Red 1
N-乙基-N-(2-羟乙基)-4-(4-硝基苯基偶氮)苯胺
分散红 1
CAS Number
2872-52-8
EC Number
220-704-3
MDL Number
MFCD00007312
Beilstein Number
5353614
PubChem SID
162233302
24861232
24847001
PubChem CID
17886
Color Index Number
11110

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
PubChem 17886 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 15.579251  H Acceptors
H Donor LogD (pH = 5.5) 4.0935307 
LogD (pH = 7.4) 4.093869  Log P 4.0938735 
Molar Refractivity 93.1712 cm3 Polarizability 32.56214 Å3
Polar Surface Area 94.01 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Melting Point
160-162 °C(lit.) expand Show data source
Absorption Wavelength
λmax 502 nm expand Show data source
λmax 503 nm expand Show data source
RTECS
KL0320000 expand Show data source
European Hazard Symbols
Irritant Irritant (Xi) expand Show data source
MSDS Link
Download expand Show data source
Download expand Show data source
Download expand Show data source
Download expand Show data source
German water hazard class
3 expand Show data source
Risk Statements
43 expand Show data source
Safety Statements
36/37 expand Show data source
GHS Pictograms
GHS07 expand Show data source
GHS Signal Word
Warning expand Show data source
GHS Hazard statements
H317 expand Show data source
GHS Precautionary statements
P280 expand Show data source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Faceshields, Gloves expand Show data source
Purity
≥96.0% (HPLC) expand Show data source
Grade
analytical standard, for food analysis expand Show data source
for microscopy expand Show data source
Compostion
Dye content, 50% expand Show data source
Dye content, 95% expand Show data source
Empirical Formula (Hill Notation)
C16H18N4O3 expand Show data source

DETAILS

DETAILS

Sigma Aldrich Sigma Aldrich
Sigma Aldrich - 344206 external link
Application
NLO material
Features and Benefits
This benchmark dipolar chromophore was incorporated into aromatic polymers to obtain model electrooptic polymer films.1
Packaging
5, 25 g in poly bottle
Sigma Aldrich - 215740 external link
Features and Benefits
This benchmark dipolar chromophore was incorporated into aromatic polymers to obtain model electrooptic polymer films.1
Sigma Aldrich - 17997 external link
Features and Benefits
This benchmark dipolar chromophore was incorporated into aromatic polymers to obtain model electrooptic polymer films.1
Other Notes
Dye standard for the assay of allergy-inducing dyes in textiles 2,3
Sigma Aldrich - 11074 external link
Features and Benefits
This benchmark dipolar chromophore was incorporated into aromatic polymers to obtain model electrooptic polymer films.1

REFERENCES

REFERENCES

From Suppliers Google Scholar IconGoogle Scholar PubMed iconPubMed Google Books IconGoogle Books
    No data available
  • Searching...Please wait...

PATENTS

PATENTS

PubChem iconPubChem Patent Google Patent Search IconGoogle Patent

INTERNET

INTERNET

Baidu iconBaidu google iconGoogle