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(S)-2,2'-Diamino-1,1'-binaphthalene

(S)-2,2'-Diamino-1,1'-binaphthalene - CAS 18531-95-8

Name: (S)-2,2'-Diamino-1,1'-binaphthalene
Brand: BOC Sciences
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(S)-2,2'-Diamino-1,1'-binaphthalene (CAS# 18531-95-8) is a useful research chemical.

Catalog Number

BCC-00028

CAS

18531-95-8

IUPAC Name

1-(2-aminonaphthalen-1-yl)naphthalen-2-amine

Synonyms

1-(2-amino-1-naphthalenyl)-2-naphthalenamine; 1-(2-aminonaphthalen-1-yl)naphthalen-2-amine

Molecular Weight

284.35

Molecular Formula

C20H16N2

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CanonicalSMILES

Canonical SMILES

InChI

InChI

InChIKey

InChI Key

Purity

Purity

MDL

MDL

Shipping

Shipping

Formulation

Formulation

PhysicalState

Physical State

Appearance

Appearance

Storage

Storage

BoilingPoint

Boiling Point

MeltingPoint

Melting Point

FlashPoint

Flash Point

Density

Density

OpticalActivity

Optical Activity

Solubility

Solubility

pKValues

pK Values

RefractiveIndex

Refractive Index

HazardClass

Hazard Class

TSCA

TSCA

WGKGermany

WGK Germany

PackingGroups

Packing Groups

Physicochemical Properties

RelatedCASValue

?Related CAS

CanonicalSMILES

Canonical SMILES

InChI

InChI

InChIKey

InChI Key

Purity

Purity

MDL

MDL

Shipping

Shipping

Formulation

Formulation

PhysicalState

Physical State

Appearance

Appearance

Storage

Storage

BoilingPoint

Boiling Point

MeltingPoint

Melting Point

FlashPoint

Flash Point

Density

Density

OpticalActivity

Optical Activity

Solubility

Solubility

pKValues

pK Values

RefractiveIndex

Refractive Index

HazardClass

Hazard Class

TSCA

TSCA

WGKGermany

WGK Germany

PackingGroups

Packing Groups

Reference Reading

1. The interaction of r(+)- or s(-)-2,2'-diamino-1,1'-binaphthalene with a pd/silica catalyst in tetrahydrofuran.

G E Robinson, G Webb, N C Young, S D Jackson. Enantiomer. 2000 Dec; 5(6): 567-70. PMID: 11342292.

The interaction of 2,2'-diamino-1,1'-binaphthalene over a Pd/silica catalyst and its interaction with hydrogen in the system and with the solvent tetrahydrofuran, (THF) has been investigated. Three interactions have been identified, i) conversion of amine groups to hydroxy groups, ii) hydrogenation of one or more of the aromatic rings, and iii) reaction between the amine group(s) and the THF solvent.

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