2-Quinolinecarboxaldehyde,oxime

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Names

[ CAS No. ]:
1131-68-6

[ Name ]:
2-Quinolinecarboxaldehyde,oxime

[Synonym ]:
2-Quinolinecarboxaldehyde,oxime
2-formaldoximoquinoline
QUINOLINALDEHYDE,OXIME
Quinaldaldehyde,oxime
2-Quinolinaldoxime
2-quinolinealdoxime
Quinoline-2-aldoxime
2-quinolinecarbaldehyde oxime
EINECS 214-471-7
Quinoline-2-carbaldehyde oxime
Quinolyl-2-aldoxime

Chemical & Physical Properties

[ Density]:
1.2g/cm3

[ Boiling Point ]:
294.6ºC at 760mmHg

[ Molecular Formula ]:
C10H8N2O

[ Molecular Weight ]:
172.18300

[ Flash Point ]:
132ºC

[ Exact Mass ]:
172.06400

[ PSA ]:
45.48000

[ LogP ]:
2.04290

[ Vapour Pressure ]:
0.00161mmHg at 25°C

[ Index of Refraction ]:
1.623

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
VA9120000
CHEMICAL NAME :
Quinolinaldehyde, oxime
CAS REGISTRY NUMBER :
1131-68-6
LAST UPDATED :
198609
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C10-H8-N2-O
MOLECULAR WEIGHT :
172.20
WISWESSER LINE NOTATION :
T66 BNJ C1UNQ

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intravenous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
56 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
CSLNX* U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. (Aberdeen Proving Ground, MD 21010) Volume(issue)/page/year: NX#09224

Safety Information

[ HS Code ]:
2933499090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • Quinoline-2-carboxaldehyde

DownStream

  • 1-quinolin-2-ylmethanamine

Customs

[ 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%

Related Compounds

  • (E)-2-quinolinecarbaldehyde oxime
  • 2-chloro-3-quinolinecarboxaldehyde oxime
  • 2-Quinolinecarboxaldehyde,4-methoxy-6,8-dimethyl-(9CI)
  • 2-Quinolinecarboxaldehyde,4-methoxy-6-methyl-(9CI)
  • 2-Quinolinecarboxaldehyde,4-methoxy-7-methyl-(9CI)
  • 2-quinolinecarboxaldehyde Schiff base S-benzyldithiocarbazate
  • 1,3-dimethyl-N-(2-(methylsulfonyl)phenyl)-1H-pyrazole-5-carboxamide
  • N-(benzo[d]thiazol-2-yl)-1,3-dimethyl-N-(pyridin-2-ylmethyl)-1H-pyrazole-5-carboxamide
  • N-(6-fluorobenzo[d]thiazol-2-yl)-1,3-dimethyl-N-(pyridin-2-ylmethyl)-1H-pyrazole-5-carboxamide
  • N-(4-fluorobenzo[d]thiazol-2-yl)-1,3-dimethyl-N-(pyridin-2-ylmethyl)-1H-pyrazole-5-carboxamide
  • N-(4,6-difluorobenzo[d]thiazol-2-yl)-1,3-dimethyl-N-(pyridin-2-ylmethyl)-1H-pyrazole-5-carboxamide
  • N-(5-chloro-4-methylbenzo[d]thiazol-2-yl)-1,3-dimethyl-N-(pyridin-2-ylmethyl)-1H-pyrazole-5-carboxamide
  • N-(4-fluorobenzo[d]thiazol-2-yl)-1,3-dimethyl-N-(pyridin-3-ylmethyl)-1H-pyrazole-5-carboxamide
  • N-(6-fluorobenzo[d]thiazol-2-yl)-1,3-dimethyl-N-(pyridin-3-ylmethyl)-1H-pyrazole-5-carboxamide
  • N-(4,7-dimethoxybenzo[d]thiazol-2-yl)-1,3-dimethyl-N-(pyridin-3-ylmethyl)-1H-pyrazole-5-carboxamide
  • N-(benzo[d]thiazol-2-yl)-1,3-dimethyl-N-((tetrahydrofuran-2-yl)methyl)-1H-pyrazole-5-carboxamide
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