1-propan-2-yl-10H-phenothiazine

Base Information

Chemical Name:1-propan-2-yl-10H-phenothiazine
CAS No.:7240-76-8
Molecular Formula:C₂₀H₂₅N₂O*I
Molecular Weight:436.336
Hs Code.:
DSSTox Substance ID:DTXSID20413759
Nikkaji Number:J610.260C
Wikidata:Q82222107

Synonyms:7240-76-8;1-propan-2-yl-10H-phenothiazine;isopropylphenothiazine;1-i-Propyl-10H-phenothiazine;SCHEMBL8749550;DTXSID20413759;GFQLUVZOBVGUCM-UHFFFAOYSA-N

Suppliers and Price of 1-propan-2-yl-10H-phenothiazine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of 1-propan-2-yl-10H-phenothiazine

Chemical Property:

Vapor Pressure:3.76E-06mmHg at 25°C
Boiling Point:385.6°Cat760mmHg
Flash Point:187°C
Density:1.14g/cm³
XLogP3:4.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:241.09252066
Heavy Atom Count:17
Complexity:266

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C1=C2C(=CC=C1)SC3=CC=CC=C3N2

Technology Process of 1-propan-2-yl-10H-phenothiazine

There total 15 articles about 1-propan-2-yl-10H-phenothiazine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 79228-07-2
(2R,12bS)-3-Eth-(E)-ylidene-4-oxo-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizine-2-carbaldehyde

: 7240-76-8,80264-66-0,107893-05-0
C₂₀H₂₅N₂O⁽¹⁺⁾*I^(1-)

Guidance literature:: Multi-step reaction with 13 steps

1: BF₃*Et₂O / CH₂Cl₂ / 0 °C

2: i-Bu₂AlH / 1,2-dimethoxy-ethane / -55 °C

3: NaBH₃CN / tetrahydrofuran / from -70 up to room temp.

4: CH₃I, CaCO₃ / H₂O; acetone / Ambient temperature

5: H₂O; tetrahydrofuran

6: CH₂Cl₂; pyridine

7: LiCl / dimethylformamide / 110 °C

8: 64 percent / NaH / dimethylsulfoxide / Ambient temperature

9: 54 percent / 1-chlorobenzotriazole, Et₃N / CH₂Cl₂ / Ambient temperature

10: KOH / aq. ethanol

11: BF₃

12: LiAlH₄

13: methanol

With potassium hydroxide; lithium aluminium tetrahydride; boron trifluoride diethyl etherate; boron trifluoride; sodium hydride; diisobutylaluminium hydride; sodium cyanoborohydride; triethylamine; N-chlorobenzotriazole; calcium carbonate; lithium chloride; methyl iodide; In tetrahydrofuran; pyridine; methanol; 1,2-dimethoxyethane; ethanol; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; acetone;
DOI:10.1016/S0040-4039(01)90397-1

Reference yield:

: 79235-45-3
(2R,12bS)-2-[1,3]Dithiolan-2-yl-3-eth-(E)-ylidene-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizine

: 7240-76-8,80264-66-0,107893-05-0
C₂₀H₂₅N₂O⁽¹⁺⁾*I^(1-)

Guidance literature:: Multi-step reaction with 11 steps

1: NaBH₃CN / tetrahydrofuran / from -70 up to room temp.

2: CH₃I, CaCO₃ / H₂O; acetone / Ambient temperature

3: H₂O; tetrahydrofuran

4: CH₂Cl₂; pyridine

5: LiCl / dimethylformamide / 110 °C

6: 64 percent / NaH / dimethylsulfoxide / Ambient temperature

7: 54 percent / 1-chlorobenzotriazole, Et₃N / CH₂Cl₂ / Ambient temperature

8: KOH / aq. ethanol

9: BF₃

10: LiAlH₄

11: methanol

With potassium hydroxide; lithium aluminium tetrahydride; boron trifluoride; sodium hydride; sodium cyanoborohydride; triethylamine; N-chlorobenzotriazole; calcium carbonate; lithium chloride; methyl iodide; In tetrahydrofuran; pyridine; methanol; ethanol; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide; acetone;
DOI:10.1016/S0040-4039(01)90397-1

Reference yield:

: 80249-88-3
C₁₉H₂₁N₃O

: 7240-76-8,80264-66-0,107893-05-0
C₂₀H₂₅N₂O⁽¹⁺⁾*I^(1-)

Guidance literature:: Multi-step reaction with 3 steps

1: BF₃

2: LiAlH₄

3: methanol

With lithium aluminium tetrahydride; boron trifluoride; In methanol;
DOI:10.1016/S0040-4039(01)90397-1