Indoline structure
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Common Name | Indoline | ||
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CAS Number | 496-15-1 | Molecular Weight | 119.164 | |
Density | 1.0±0.1 g/cm3 | Boiling Point | 227.2±10.0 °C at 760 mmHg | |
Molecular Formula | C8H9N | Melting Point | -21 °C | |
MSDS | Chinese USA | Flash Point | 92.8±0.0 °C |
Name | indoline |
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Synonym | More Synonyms |
Density | 1.0±0.1 g/cm3 |
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Boiling Point | 227.2±10.0 °C at 760 mmHg |
Melting Point | -21 °C |
Molecular Formula | C8H9N |
Molecular Weight | 119.164 |
Flash Point | 92.8±0.0 °C |
Exact Mass | 119.073502 |
PSA | 12.03000 |
LogP | 1.63 |
Vapour Pressure | 0.1±0.4 mmHg at 25°C |
Index of Refraction | 1.562 |
Storage condition | 2-8°C |
Water Solubility | 5 g/L (20 ºC) |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Personal Protective Equipment | Eyeshields;Gloves;half-mask respirator (US);multi-purpose combination respirator cartridge (US) |
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Hazard Codes | Xi:Irritant |
Risk Phrases | R36/37/38 |
Safety Phrases | S23-S24/25-S37/39-S26 |
WGK Germany | 3 |
RTECS | NL6906300 |
HS Code | 2933990090 |
Precursor 9 | |
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DownStream 10 | |
HS Code | 2933990090 |
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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% |
Palladium-catalyzed insertion of N-tosylhydrazones for the synthesis of isoindolines.
Chem. Commun. (Camb.) 49(31) , 3254-6, (2013) Isoindolines are synthesized by palladium-catalyzed coupling reaction of N-(2-iodobenzyl) anilines with α,β-unsaturated N-tosylhydrazones. The reaction has several potential advantages: (1) toleration... |
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FeCl3-mediated Friedel-Crafts hydroarylation with electrophilic N-acetyl indoles for the synthesis of benzofuroindolines.
Angew. Chem. Int. Ed. Engl. 51(50) , 12546-50, (2012) IRONic electrophilic indoles! The C3-regioselective hydroarylation of N-acetyl indoles with aromatic nucleophiles mediated by FeCl(3) features a rare example of the electrophilic reactivity of the ind... |
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Identification and Testing of Novel CARP-1 Functional Mimetic Compounds as Inhibitors of Non-Small Cell Lung and Triple Negative Breast Cancers.
J. Biomed. Nanotechnol. 11 , 1608-27, (2015) The triple negative breast cancer (TNBCs) and non-small cell lung cancers (NSCLCs) often acquire mutations that contribute to failure of drugs in clinic and poor prognosis, thus presenting an urgent n... |
2,3-dihydro-1H-1-indole |
Indoline |
IDN |
trans-dihydroindole |
2,3-dihydro-1H-indole |
EINECS 207-816-8 |
MFCD00005705 |
2,3-DIHYDROINDOLE |
1H-Indole, 2,3-dihydro- |
1-Azaindan |
2,3-Dihydro-1H-indol |
dihydroindole |