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10349-22-1

2-Naphthalenol, 1-[[(1-phenylethyl)imino]methyl]-, (R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 10349-22-1 Structure

  • Basic information

    1. Product Name: 2-Naphthalenol, 1-[[(1-phenylethyl)imino]methyl]-, (R)-
    2. Synonyms:
    3. CAS NO:10349-22-1
    4. Molecular Formula: C19H17NO
    5. Molecular Weight: 275.35
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10349-22-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Naphthalenol, 1-[[(1-phenylethyl)imino]methyl]-, (R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Naphthalenol, 1-[[(1-phenylethyl)imino]methyl]-, (R)-(10349-22-1)
    11. EPA Substance Registry System: 2-Naphthalenol, 1-[[(1-phenylethyl)imino]methyl]-, (R)-(10349-22-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 10349-22-1(Hazardous Substances Data)

10349-22-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10349-22-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,4 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10349-22:
(7*1)+(6*0)+(5*3)+(4*4)+(3*9)+(2*2)+(1*2)=71
71 % 10 = 1
So 10349-22-1 is a valid CAS Registry Number.

10349-22-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-N-(1-phenylethyl)-2-hydroxy-1-naphthaldimine

1.2 Other means of identification

Product number -
Other names (R)-N-1-(phenyl)ethyl-2-oxo-1-naphthaldimine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10349-22-1 SDS

10349-22-1Downstream Products

10349-22-1Relevant articles and documents

A simple and effective fluorescent chemosensor for the cascade recognition of Zn2+ and H2PO4- ions in protic media

Zhang, Mengyu,Lu, Wei,Zhou, Jinting,Du, Ganhong,Jiang, Liming,Ling, Jun,Shen, Zhiquan

, p. 1011 - 1015 (2014)

The chiral Schiff base N-(2-hydroxy-1-naphthyl)methylidene-(S)-α- phenylethylamine (1) was designed and synthesized as a fluorescent chemosensor based on the photoinduced electron transfer (PET) and CN isomerization mechanisms. The receptor exhibited a highly selective switch-on fluorescence response toward Zn2+ and especially avoided the interference of Cd2+ when the detection was conducted in unbuffered methanol solution. Furthermore, the in situ generated 1·ZnII-complex could be employed for the specific recognition of H2PO 4- by fluorescence turn-off signaling through a ligand displacement process.

Synthesis, spectroscopy, catalysis and crystal structure of [Rh(η4-cod){(R)-N-(Ar)ethyl-2-oxo-1-naphthaldiminato- κ2N,O}] (Ar = C6H5, 3-/4-MeOC 6H4, and 4-BrC6H4)

Enamullah, Mohammed,Royhan Uddin,Hogarth, Graeme,Janiak, Christoph

experimental part, p. 173 - 180 (2012/06/30)

Condensation of 2-hydroxy-1-naphthaldehyde with (R)-(Ar)ethylamine yields the enantiopure Schiff bases, (R)-N-(Ar)ethyl-2-hydroxy-1-naphthaldimine (Ar = C6H5, 3-/4-MeOC6H4, 4-BrC 6H4). Thes

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