Product Name:	(2R,5R)-1,6-Diphenylhexane-2,5-diaMine dihydrochloride
Synonyms:	(2R,5R)-1,6-Diphenylhexane-2,5-diaMinedihydrochloride;(2R,5R)-1,6-Diphenyl-2,5-hexanediaMinehydrochloride; (2R,5R)-1,6-diphenylhexane-2,5-diaMine;2,5-Hexanediamine,1,6-diphenyl-,hydrochloride(1:2),(2R,5R)-; (2R,5R)-1,6-DIPHENYLChemicalbookHEXANE-2,5-DIAMINE2HCL; (2R,5R)-1,6-Diphenylhexane-2,5-diamine2HydrochloricAcidSalt; FAVORITESCOMPARE(2R,5R)-1,6-DIPHENYLHEXANE-2,5-DIAMINEDIHYDROCHLORIDE1247119-31-8; (2R,5R)-1,6-Diphenyl-hexane-2,5-Diamine,?dihydrogen?chloride
CAS:	1247119-31-8
MF:	C18H25ClN2
MW:	304.8575
EINECS	700-856-1

(2R,5R)-1,6-Diphenylhexane-2,5-diaMine dihydrochloride

Melting point	>200°C (Dec.)
Solubility	DMSO (slight, with heating, ultrasound), methanol (slight), water (slight, with heating)
Storage temp.	Inert atmosphere,Room Temperature

Form	Solid
Color	White to off-white

Usage

Uses

1. Asymmetric Catalysis / Chiral Ligand

Serves as a chiral diamine ligand or precursor, used to construct highly efficient chiral metal catalysts, and is widely applied in highly selective reactions such as asymmetric hydrogenation and addition reactions.

2. Pharmaceutical Intermediate

Used in the synthesis of chiral drugs, chiral alkaloids, or central nervous system (CNS) drugs, and is an important synthetic building block for constructing chiral pharmacophores or stereocenters.

3. Organic Synthesis & Scientific Research

Employed in research on asymmetric synthesis methodologies, development of novel catalytic systems, and the construction of natural products and drug molecules, and holds significant scientific and innovative value.

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