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Acetamide, N,N'-[1,1'-binaphthalene]-2,2'-diylbis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

93621-65-9

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93621-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93621-65-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,6,2 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 93621-65:
(7*9)+(6*3)+(5*6)+(4*2)+(3*1)+(2*6)+(1*5)=139
139 % 10 = 9
So 93621-65-9 is a valid CAS Registry Number.

93621-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[1-(2-acetamidonaphthalen-1-yl)naphthalen-2-yl]acetamide

1.2 Other means of identification

Product number -
Other names 1,1'-Binaphthyl,2,2'-diacetamido

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:93621-65-9 SDS

93621-65-9Relevant academic research and scientific papers

AXIALLY DISSYMMETRIC bis(AMINOPHOSPHINE)S DERIVED FROM 2,2 prime -DIAMINO-1,1 prime -BINAPHTHYL. SYNTHESIS AND APPLICATION TO RHODIUM(I)-CATALYZED ASYMMETRIC HYDROGENATIONS.

Miyano,Nawa,Mori,Hashimoto

, p. 2171 - 2176 (2007/10/02)

Axially dissymmetric bisphosphine ligands, (R)- and (S)-2,2 prime -bis(diphenylphosphinoamino)-1,1 prime -binaphthyl (BDPAB) and (R)-2,2 prime -bis left bracket N-(diphenylphosphino)methylamino right bracket -1,1 prime -binaphthyl (Me-BDPAB) were conveniently prepared from 2,2 prime -diamino-1,1 prime -binaphthyl. The rhodium(I)-catalyzed asymmetric hydrogenation of alpha -acylamidoacrylic acids and esters gave the corresponding amino acids of up to 95% optical purity. The sign of the centro-chirality of the product amino acids was always the same to that of axial chirality of the ligand in both cases of BDPAB and Me-BDPAB.

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