4,7-Dichloroquinoline structure
|
Common Name | 4,7-Dichloroquinoline | ||
---|---|---|---|---|
CAS Number | 86-98-6 | Molecular Weight | 198.05 | |
Density | 1.4±0.1 g/cm3 | Boiling Point | 292.9±20.0 °C at 760 mmHg | |
Molecular Formula | C9H5Cl2N | Melting Point | 81-83 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 158.7±7.4 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of 4,7-Dichloroquinoline4,7-Dichloroquinoline is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
Name | 4,7-Dichloroquinoline |
---|---|
Synonym | More Synonyms |
Description | 4,7-Dichloroquinoline is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
---|---|
Related Catalog |
Density | 1.4±0.1 g/cm3 |
---|---|
Boiling Point | 292.9±20.0 °C at 760 mmHg |
Melting Point | 81-83 °C(lit.) |
Molecular Formula | C9H5Cl2N |
Molecular Weight | 198.05 |
Flash Point | 158.7±7.4 °C |
Exact Mass | 196.979904 |
PSA | 12.89000 |
LogP | 3.46 |
Vapour Pressure | 0.0±0.6 mmHg at 25°C |
Index of Refraction | 1.661 |
Water Solubility | insoluble |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
MUTATION DATA
|
Symbol |
GHS07 |
---|---|
Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi:Irritant |
Risk Phrases | R36/37/38 |
Safety Phrases | S26-S36-S22 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | VB4200000 |
HS Code | 2933499013 |
Precursor 9 | |
---|---|
DownStream 10 | |
HS Code | 2933499090 |
---|---|
Summary | 2933499090. other compounds containing in the structure a quinoline or isoquinoline ring-system (whether or not hydrogenated), not further fused. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
New bioactive compounds from Aloe hijazensis.
Nat. Prod. Res. 23 , 1035-1049, (2009) The chemical constituents and biological activities of leaves and roots of Aloe hijazensis, collected in Saudi Arabia, are reported here for the first time. Twenty-two compounds were obtained, among t... |
|
Direct, catalytic, and regioselective synthesis of 2-alkyl-, aryl-, and alkenyl-substituted N-heterocycles from N-oxides.
Org. Lett. 16(3) , 864-7, (2014) A one-step transformation of heterocyclic N-oxides to 2-alkyl-, aryl-, and alkenyl-substituted N-heterocycles is described. The success of this broad-scope methodology hinges on the combination of cop... |
|
"One-pot" synthesis and antimalarial activity of formamidine derivatives of 4-anilinoquinoline.
Chem. Pharm. Bull. 49(8) , 933-7, (2001) Amodiaquine (AQ) is an antimalarial which is effective against chloroquino-resistant strains of Plasmodium falciparum but whose clinical use is severely restricted because of associated hepatotoxicity... |
Quinoline, 4,7-dichloro- |
4,7- Dichloroquinoline |
4,7-DICHLORO QUINOLINE |
4,7-DICHLORCHINOLIN |
4,7-Dichloroquinoline,tech. |
4,7-dichloroquinolne |
4,7-DICHLOROQUINOLINE FOR SYNTHESIS |
7-Dichloroquinoline |
TL 1473 |
4 7-DICHLOROQUINOLINE |
Chloroquine Related Compound A (25 mg) (4,7-dichloroquinoline) |
4,7-Dichloroquinoline |
4,7-DICHLOROQUINOLI |
4,7-dichloro-quinolin |
4.7-dichloroquinoline |
4,7-Dichlor-chinolin |
4,7-DICHLOLROQUINOLINE |
EINECS 201-714-7 |
MFCD00006774 |