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885701-71-3

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  • Phenyl-[(S)-1,1-spirobiindane-7,7-diyl]-phosphite, (11aS)-(-)-10,11,12,13-Tetrahydrodiindeno[7,1-de:1μ,7μ-fg][1,3,2]dioxaphosphocin-5-phenoxy

    Cas No: 885701-71-3

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  • (11aS)-(-)-10,11,12,13-Tetrahydrodiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-phenoxy, min. 98% (S)-ShiP

    Cas No: 885701-71-3

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885701-71-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 885701-71-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,7,0 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 885701-71:
(8*8)+(7*8)+(6*5)+(5*7)+(4*0)+(3*1)+(2*7)+(1*1)=203
203 % 10 = 3
So 885701-71-3 is a valid CAS Registry Number.

885701-71-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Phenoxy-10,11,12,13-tetrahydrodiindeno[7,1-de:1',7'-fg][1,3,2]d ioxaphosphocine

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

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

More Details:885701-71-3 SDS

885701-71-3Downstream Products

885701-71-3Relevant articles and documents

Highly regioselective asymmetric copper-catalyzed allylic alkylation with dialkylzincs using monodentate chiral spiro phosphoramidite and phosphite ligands

Shi, Wen-Jian,Wang, Li-Xin,Fu, Yu,Zhu, Shou-Fei,Zhou, Qi-Lin

, p. 3867 - 3872 (2003)

The copper complexes of chiral spiro phosphoramidite and phosphite ligands were found to be effective catalysts in the asymmetric allylic alkylations of cinnamyl halides with dialkylzincs. The allylic alkylation products were obtained in high regioselecti

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