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ChemicalBook--->CAS DataBase List--->161829-92-1

161829-92-1

161829-92-1 Structure

161829-92-1 Structure
IdentificationBack Directory
[Name]

CIS-HEXAHYDROISOINDOLINE HYDROGEN CHLORIDE
[CAS]

161829-92-1
[Synonyms]

Cis-hexahydroisoindolineHCL
Cis-hexahydroisoindole, HCl
cis-Octahydroisoindole hydrochloride
Cis-Hexahydroisoindoline hydrochloride
CIS-HEXAHYDROISOINDOLINE HYDROGEN CHLORIDE
(3aR,7aS)-octahydro-1H-isoindole hydrochloride
(3aR,7aS)-rel-Octahydro-1H-isoindole hydrochloride
rel-(3aR,7aS)-Octahydro-1H-isoindole hydrochloride
(3aR,7aS)-octahydro-1H-isoindole hydrochloride (1:1)
(3aR,7aS)-rel-octahydro-1H-Isoindole, hydrochloride (1:1)
1H-Isoindole,octahydro-, hydrochloride, (3aR,7aS)-rel- (9CI)
(3aR,7aS)-2,3,3a,4,5,6,7,7a-Octahydro-1H-isoindole hydrochloride
5-[2-(4-{[(1S)-4-ethoxy-1-(ethoxycarbonyl)-4-oxobutyl]carbamoyl}phenyl)ethyl]-4-oxo-4,7-dihydro-1H-pyrrolo[2,3-d]pyrimidin-2-aminium
[EINECS(EC#)]

1806241-263-5
[Molecular Formula]

C8H16ClN
[MDL Number]

MFCD09026400
[MOL File]

161829-92-1.mol
[Molecular Weight]

161.672
Chemical PropertiesBack Directory
[Melting point ]

121-123 °C
[storage temp. ]

Sealed in dry,Room Temperature
[InChI]

InChI=1/C8H15N.ClH/c1-2-4-8-6-9-5-7(8)3-1;/h7-9H,1-6H2;1H/t7-,8+;
[InChIKey]

CLQIZUYXKFTUEB-KVZVIFLMNA-N
[SMILES]

[H][C@]12CCCC[C@@]1([H])CNC2.Cl |&1:1,6,r|
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P233-P260-P261-P264-P271-P280-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
[HS Code ]

2933998090
Hazard InformationBack Directory
[Description]

Cis-Octahydro-1H-isoindole hydrochloride is an important intermediate in the synthesis of mitiglinide which is a new oral hypoglycemic drug for the treatment of type II diabetes for the first marked in Japan
[Preparation]

Phthalimide was used as raw material to react with KOH. Benzyl bromide was subsequently added to the solution to obtain the N-benzylphthalimide. The addition of lithium tetrahydroaluminum, reducing compound N-benzylphthalimide, yields N-benzyldihydroisoindole. Finally, cis-Octahydro-1H-isoindole hydrochlorid is obtained by Pd/C catalysis and reduction
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