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1,1'-Binaphthalene, 2-iodo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

402745-52-2

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402745-52-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 402745-52-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,2,7,4 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 402745-52:
(8*4)+(7*0)+(6*2)+(5*7)+(4*4)+(3*5)+(2*5)+(1*2)=122
122 % 10 = 2
So 402745-52-2 is a valid CAS Registry Number.

402745-52-2SDS

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 2-iodo-1-naphthalen-1-ylnaphthalene

1.2 Other means of identification

Product number -
Other names 2-iodo-1,1'-binaphthyl

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:402745-52-2 SDS

402745-52-2Upstream product

402745-52-2Relevant academic research and scientific papers

Further Structural Modification of Sulfur-Stabilized Silicon Cations with Binaphthyl Backbones

Shaykhutdinova, Polina,Oestreich, Martin

, p. 2221 - 2229 (2019)

The synthesis and spectroscopic characterization of two novel cationic silicon-sulfur Lewis pairs with a chiral 4,4′-disubstituted binaphthyl silepine backbone are described. Both Lewis acids induce significant enantioselectivity in the model Diels-Alder reaction of cyclohexa-1,3-diene and chalcone but additional substitution of the binaphthyl backbone exerts a minimal effect on enantioinduction compared to previously reported Lewis acids. Another silicon cation with a chiral spirocyclic backbone induces enantioselectivity in the same range but its synthesis is laborious.

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