ChemicalBook--->CAS DataBase List--->57196-61-9

57196-61-9

57196-61-9 Structure

57196-61-9 Structure
IdentificationBack Directory
[Name]

2-methyl-1,2,3,4-tetrahydroisoquinolin-2-ium-4,6-diol,chloride
[CAS]

57196-61-9
[Synonyms]

1,2,3,4-Tetrahydro-4,6-dihydroxy-2-
1,2,3,4-Tetrahydro-4,6-dihydroxy-2-methylisoquinoline HCl
2-methyl-1,2,3,4-tetrahydroisoquinolin-2-ium-4,6-diol,chloride
PhenylephrineHCl(1,2,3,4-tetrahydro-4,6-di hydroxy 2-methyl isoquinoline
PhenylephrineHCl(1,2,3,4-tetrahydro-4,8-di hydroxy 2-methyl isoquinoline
(4R)-4,6-DIHYDROXY-N-METHYL-1,2,3,4- TETRAHYDROISOQUINOLINE HYDROCHLORIDE
1,2,3,4-Tetrahydro-4,6-dihydroxy-2-methyl-isoquinoline HydrochlorideQ: What is 1,2,3,4-Tetrahydro-4,6-dihydroxy-2-methyl-isoquinoline Hydrochloride Q: What is the CAS Number of 1,2,3,4-Tetrahydro-4,6-dihydroxy-2-methyl-isoquinoline Hydrochloride Q: What is the storage condition of 1,2,3,4-Tetrahydro-4,6-dihydroxy-2-methyl-isoquinoline Hydrochloride Q: What are the applications of 1,2,3,4-Tetrahydro-4,6-dihydroxy-2-methyl-isoquinoline Hydrochloride
[Molecular Formula]

C10H14ClNO2
[MOL File]

57196-61-9.mol
[Molecular Weight]

215.677
Chemical PropertiesBack Directory
[Melting point ]

186-190°C (lit.)
[storage temp. ]

2-8°C
[solubility ]

soluble in Water; Methanol
[form ]

Solid
[color ]

White
[Major Application]

pharmaceutical small molecule
[InChI]

1S/C10H13NO2.ClH/c1-11-5-7-2-3-8(12)4-9(7)10(13)6-11;/h2-4,10,12-13H,5-6H2,1H3;1H
[InChIKey]

NQWCCJZOYHZSNW-UHFFFAOYSA-N
[SMILES]

[Cl-].[N+H]1(CC(c2c(ccc(c2)O)C1)O)C
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

2-Methyl-1,2,3,4-tetrahydro-4,(6,8)-isoquinolinediol Hydrochloride (Mixture of Isomers) is a product formed during the decomposition of Phenylephrine.
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