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1380575-45-0

1380575-45-0 Structure

1380575-45-0 Structure
IdentificationBack Directory
[Name]

5-Methyl-2-(1-Methylethoxy)-4- (4-piperidinyl)- BenzenaMine hydrochloride (1:2)
[CAS]

1380575-45-0
[Synonyms]

CR-14
LDK378 intermediate
5-Methyl-2-(1-Methylethoxy)-4-
2-Isopropoxy-5-methyl-4-(4-piperidyl)aniline Dihydrochloride
2-isopropoxy-5-methyl-4-(piperidin-4-yl)aniline hydrochloride
2-isopropoxy-5-Methyl-4-(piperidin-4-yl)aniline dihydrochloride
2-isopropoxy-5-methyl-4-(piperdin-4-yl) aniline dihydrochloride
2-ISOPROPOXY-5-METHYL-4-(PIPERIDINE-4- - YL)ANILINE DIHYDROCHLORIDE
(1-Methylethoxy)-4-(4-piperidinyl)- BenzenaMine hydrochloride (1:2)
5-methyl-4-(piperidin-4-yl)-2-(propan-2-yloxy)aniline dihydrochloride
5-methyl-2-(1-methylethoxy)-4-(4-piperidinyl)-phenylamine dihydrochloride
5-Methyl-2-(1-Methylethoxy)-4- (4-piperidinyl)- BenzenaMine hydrochloride
5-methyl-2-(1-methylethoxy)-4-(4-piperidinyl)- benzenamine (dihydrochloride)
5-Methyl-2-(1-Methylethoxy)-4- (4-piperidinyl)- BenzenaMine hydrochloride (1:2)
Benzenamine, 5-methyl-2-(1-methylethoxy)-4-(4-piperidinyl)- (hydrochloride)(1:2)
[Molecular Formula]

C15H26Cl2N2O
[MDL Number]

MFCD28387189
[MOL File]

1380575-45-0.mol
[Molecular Weight]

321.286
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C15H24N2O.ClH/c1-10(2)18-15-9-13(11(3)8-14(15)16)12-4-6-17-7-5-12;/h8-10,12,17H,4-7,16H2,1-3H3;1H
[InChIKey]

MUIYMJXNFJYXFP-UHFFFAOYSA-N
[SMILES]

CC1=CC(N)=C(OC(C)C)C=C1C1CCNCC1.Cl
Hazard InformationBack Directory
[Uses]

5-Methyl-2-(1-Methylethoxy)-4-(4-piperidinyl)- BenzenaMine hydrochloride (1:2) is a chemical intermediate for the preparation of ceritinib.
[Application]

5-Methyl-2-(1-Methylethoxy)-4-(4-piperidinyl)- BenzenaMine hydrochloride (1:2) is a chemical intermediate, also known as (4-(5-isopropoxy) -2-Methyl-4-amino-phenyl)-piperidine hydrochloride can be used in laboratory R&D synthesis process and chemical biological R&D process, and is an intermediate for the preparation of ceritinib.
[Preparation]

First use methanol to react with 4-(5-isopropoxy-2-methyl-4-nitrophenyl)pyridine, and then add wet palladium carbon to finally obtain 5-Methyl-2-(1-Methylethoxy)-4-(4-piperidinyl)- BenzenaMine hydrochloride (1:2).
Spectrum DetailBack Directory
[Spectrum Detail]

5-Methyl-2-(1-Methylethoxy)-4- (4-piperidinyl)- BenzenaMine hydrochloride (1:2)(1380575-45-0)1HNMR
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