What is the 1-Phenyl-3,4-dihydroisoquinoline?

1-Phenyl-3,4-dihydroisoquinoline is , while it's Molecular Formula is C15H13N. 1-Phenyl-3,4-dihydro-isoquinoline is used in preparation of 1,2,3,4-Tetrahydro-2-methyl-1-phenyl-1-isoquinolinecarbonitrile derivatives.

What is the CAS number for 1-Phenyl-3,4-dihydroisoquinoline?

The CAS number of 1-Phenyl-3,4-dihydroisoquinoline is 52250-50-7.

What is 1-Phenyl-3,4-dihydroisoquinoline (52250-50-7) used for?

1-Phenyl-3,4-dihydroisoquinoline is an organic compound belonging to the isoquinoline family. It is characterized by its unique molecular structure, which features a phenyl group attached to a dihydroisoquinoline ring. 1-Phenyl-3,4-dihydroisoquinoline is known for its potential applications in various fields due to its chemical properties.InChI:InChI=1/C15H13N/c1-2-7-13(8-3-1)15-14-9-5-4-6-12(14)10-11-16-15/h1-9H,10-11H2

What is the 1-Phenyl-3,4-dihydroisoquinoline?

1-Phenyl-3,4-dihydroisoquinoline is , while it's Molecular Formula is C15H13N. 1-Phenyl-3,4-dihydro-isoquinoline is used in preparation of 1,2,3,4-Tetrahydro-2-methyl-1-phenyl-1-isoquinolinecarbonitrile derivatives.

What is the CAS number for 1-Phenyl-3,4-dihydroisoquinoline?

The CAS number of 1-Phenyl-3,4-dihydroisoquinoline is 52250-50-7.

What is 1-Phenyl-3,4-dihydroisoquinoline (52250-50-7) used for?

1-Phenyl-3,4-dihydroisoquinoline is an organic compound belonging to the isoquinoline family. It is characterized by its unique molecular structure, which features a phenyl group attached to a dihydroisoquinoline ring. 1-Phenyl-3,4-dihydroisoquinoline is known for its potential applications in various fields due to its chemical properties.InChI:InChI=1/C15H13N/c1-2-7-13(8-3-1)15-14-9-5-4-6-12(14)10-11-16-15/h1-9H,10-11H2

1-Phenyl-3,4-dihydroisoquinoline

CAS：52250-50-7
MF：C₁₅H₁₃N
Purity：99%
Molecular Weight：207.275

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Product Details

CAS： 52250-50-7

MF： C₁₅H₁₃N

Manufacturer supply high quality 1-Phenyl-3,4-dihydroisoquinoline 52250-50-7 with GMP standards

Molecular Formula:C15H13N
Molecular Weight:207.275
Vapor Pressure:0.000408mmHg at 25°C
Melting Point:174 °C
Refractive Index:1.611
Boiling Point:326.5 °C at 760 mmHg
PKA:5.29±0.20(Predicted)
Flash Point:143.4 °C
PSA：12.36000
Density:1.07 g/cm³
LogP:2.51570

1-Phenyl-3,4-dihydroisoquinoline(Cas 52250-50-7) Usage

InChI:InChI=1/C15H13N/c1-2-7-13(8-3-1)15-14-9-5-4-6-12(14)10-11-16-15/h1-9H,10-11H2

52250-50-7 Relevant articles

-

Parham et al.

, p. 1606 (1978)

Enhancement of the carbamate activation rate enabled syntheses of tetracyclic benzolactams: 8-oxoberbines and their 5- And 7-membered C-ring homologues

Kurouchi, Hiroaki

, p. 653 - 658 (2021/02/06)

A route to the direct amidation of aroma...

Tf2O/TTBP (2,4,6-Tri-tert-butylpyrimidine): An Alternative Amide Activation System for the Direct Transformations of Both Tertiary and Secondary Amides

He, Qian,Ye, Jian-Liang,Xu, Fang-Fang,Geng, Hui,Chen, Ting-Ting,Chen, Hang,Huang, Pei-Qiang

, (2021/09/28)

Ten types of Tf2O/TTBP-mediated amide tr...

Enantioselective Allylation of Cyclic and In Situ Formed N-Unsubstituted Imines with Tetraol-Protected Allylboronates

Ullrich, Patrick,Schlamkow, Max A.,Choi, Ching-Yi,Kerkenpa?, Hannah,Hen?en, Birgit,Pietruszka, J?rg

supporting information, p. 6254 - 6257 (2021/11/03)

Tetraol-protected α-chiral allylboronate...

Diprotonative stabilization of ring-opened carbocationic intermediates: conversion of tetrahydroisoquinoline to triarylmethanes

Kurouchi, Hiroaki

, p. 8313 - 8316 (2020/08/17)

Superacid-promoted conversion of tetrahy...

52250-50-7 Process route

: 22990-19-8
1-phenyl-1,2,3,4-tetrahydroisoquinoline

: 3297-72-1
1-phenylisoquinoline

: 52250-50-7
1-phenyl-3,4-dihydroisoquinoline

Conditions

Conditions	Yield
With potassium phosphate tribasic trihydrate; palladium on activated charcoal; oxygen; In acetonitrile; at 60 ℃; for 17h; Solvent; Temperature; Reagent/catalyst;	86%
With air; In N,N-dimethyl-formamide; at 100 ℃; for 24h; Temperature; Solvent; Concentration; Schlenk technique; Green chemistry;	83%
With sodium carbonate; In ethyl acetate; at 120 ℃; for 24h; Overall yield = 99 %; Sealed tube; Green chemistry;	77% 22%
With 1 wt % Rh⁰ photodeposited TiO₂nanoparticles; In isopropyl alcohol; at 20 ℃; for 48h; Irradiation; Inert atmosphere; Sealed tube;	56% 32%
With oxygen; 4-amino-2,2,6,6-tetramethyl-1-piperidine-1-oxyl; In isopropyl alcohol; at 20 ℃; for 24h; under 760.051 Torr; Irradiation; Sealed tube; Sonication;	54% 33%
With potassium phosphate tribasic trihydrate; 5%-palladium/activated carbon; In acetonitrile; at 60 ℃; for 22h; Reagent/catalyst; Solvent; Temperature; chemoselective reaction; Catalytic behavior; Green chemistry;

: 1-phenyl-2-tosyl-1,2,3,4-tetrahydroisoquinoline

: 3297-72-1
1-phenylisoquinoline

: 52250-50-7
1-phenyl-3,4-dihydroisoquinoline

Conditions

Conditions	Yield
With sodium hydroxide; In water; dimethyl sulfoxide; at 125 ℃; for 2h; Inert atmosphere;	83% 9%

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52250-50-7 Downstream products

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1-Phenyl-3,4-dihydroisoquinoline

Manufacturer supply high quality 1-Phenyl-3,4-dihydroisoquinoline 52250-50-7 with GMP standards

1-Phenyl-3,4-dihydroisoquinoline(Cas 52250-50-7) Usage

52250-50-7 Relevant articles

-

Parham et al.

, p. 1606 (1978)

Enhancement of the carbamate activation rate enabled syntheses of tetracyclic benzolactams: 8-oxoberbines and their 5- And 7-membered C-ring homologues

Kurouchi, Hiroaki

, p. 653 - 658 (2021/02/06)

Tf2O/TTBP (2,4,6-Tri-tert-butylpyrimidine): An Alternative Amide Activation System for the Direct Transformations of Both Tertiary and Secondary Amides

He, Qian,Ye, Jian-Liang,Xu, Fang-Fang,Geng, Hui,Chen, Ting-Ting,Chen, Hang,Huang, Pei-Qiang

, (2021/09/28)

Enantioselective Allylation of Cyclic and In Situ Formed N-Unsubstituted Imines with Tetraol-Protected Allylboronates

Ullrich, Patrick,Schlamkow, Max A.,Choi, Ching-Yi,Kerkenpa?, Hannah,Hen?en, Birgit,Pietruszka, J?rg

supporting information, p. 6254 - 6257 (2021/11/03)

Diprotonative stabilization of ring-opened carbocationic intermediates: conversion of tetrahydroisoquinoline to triarylmethanes

Kurouchi, Hiroaki

, p. 8313 - 8316 (2020/08/17)

52250-50-7 Process route

52250-50-7 Upstream products

52250-50-7 Downstream products

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