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2-Naphthalenol, 1-[4-[(1R)-1-phenylethoxy]-1-phthalazinyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

828300-87-4

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828300-87-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 828300-87-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,2,8,3,0 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 828300-87:
(8*8)+(7*2)+(6*8)+(5*3)+(4*0)+(3*0)+(2*8)+(1*7)=164
164 % 10 = 4
So 828300-87-4 is a valid CAS Registry Number.

828300-87-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[4-[(1R)-1-phenylethoxy]-2H-phthalazin-1-ylidene]naphthalen-2-one

1.2 Other means of identification

Product number -
Other names -

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:828300-87-4 SDS

828300-87-4Relevant academic research and scientific papers

Readily available biaryl P,N ligands for asymmetric catalysis

Knoepfel, Thomas F.,Aschwanden, Patrick,Ichikawa, Takashi,Watanabe, Takumi,Carreira, Erick M.

, p. 5971 - 5973 (2007/10/03)

A short and modular synthesis of novel P,N ligands (pinap; see scheme; X = O or NH) is presented. A covalently bound chiral group allows the separation of the atropisomeric diastereomers, thus avoiding resolution involving chiral Pd-amine complexes. The utility of the ligands is demonstrated for three reactions catalyzed by different transition metals; in each case products are obtained with high enantiomeric excess (up to 99% ee).

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