(+)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline
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(+)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline
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CAS No:
118864-75-8
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Formula:
C15H15N
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Chemical Name:
(+)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline
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Synonyms:
Isoquinoline,1,2,3,4-tetrahydro-1-phenyl-,(1S)-;Isoquinoline,1,2,3,4-tetrahydro-1-phenyl-,(S)-;(1S)-1,2,3,4-Tetrahydro-1-phenylisoquinoline;(S)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline;(1S)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline;(+)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline;(S)-(+)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline;(1S)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline;(-)-(S)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline;(S)-1,2,3,4-Tetrahydro-1-phenylisoquinoline
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CAS No:
Characteristics
12
3
white solid
1.1±0.1 g/cm3
80-82 °C @ Solvent: Hexane
338.4°C at 760 mmHg
166.9±14.7 °C
1.589
9.87E-05mmHg at 25°C
Safety Information
P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, P501
H302
|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P272, P273, P280, P301+P312, P302+P352, P321, P330, P333+P313, P363, P391, and P501|The GHS information provided by 1 company from 1 notification to the ECHA C&L Inventory.|H302 (20%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 16 companies from 8 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
(+)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline Use and Manufacturing
Used as an oxidation absorbent, and also used in the preparation of phosphoric acid and other phosphides. Phosphorus is divided into yellow phosphorus and red phosphorus. Yellow phosphorus (also known as white phosphorus) is used in the production of pesticides, which is the starting material for preparing all phosphorus-containing pesticide intermediates. It reacts with sulfur to obtain phosphorus pentasulfide, and reacts with chlorine to obtain phosphorus trichloride, and a series of other phosphorus-containing intermediates can be obtained. body. In addition, yellow phosphorus is mainly used for the production of phosphoric acid, and a small amount is used for the production of red phosphorus and phosphorus pentoxide. It is also used for the production of incendiary bombs and signal bombs in the military, as well as for the production of ferro-phosphorus alloys, pharmaceuticals, and organic raw materials. Uses are mainly used for the production of thermal phosphoric acid, phosphorus trichloride, phosphorus oxychloride, phosphorus pentasulfide and other phosphorus compounds, and for the manufacture of trichlorfon, methamidophos, dimethamidine, pyridoxine, dichlorvos and other organophosphorus pesticides and rodent control Raw materials for medicine. A small amount is used to produce red phosphorus and phosphorus pentoxide. Used in the military to manufacture incendiary bombs, tracer bombs, smoke bombs and signal bombs. It is also used in the production of ferro-phosphorus alloys, pharmaceuticals, organic raw materials and other industries. Uses: Used to make matches, fireworks, aluminum phosphide, phosphorus pentoxide, phosphorus trichloride, etc. It is the raw material for the production of organophosphorus pesticides. The metallurgical industry is used to make phosphor bronze sheets. It is also used for deacidification of light metals and pharmaceuticals.
Computed Properties
Molecular Weight:209.29
XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:209.120449483
Monoisotopic Mass:209.120449483
Topological Polar Surface Area:12
Heavy Atom Count:16
Complexity:220
Defined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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(+)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline
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