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Propanoic acid, 2,2-dimethyl-, (2R,3S)-4-[(2R)-2-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]-3,4-dihydro-6-[3 -[(4-methoxyphenyl)methoxy]propyl]-2-[(1E)-2-[(S)-(4-methylphenyl)sulfin yl]ethenyl]-2H-pyran-5-yl]-2,3-dimethylbutyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

851370-20-2

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851370-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 851370-20-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,3,7 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 851370-20:
(8*8)+(7*5)+(6*1)+(5*3)+(4*7)+(3*0)+(2*2)+(1*0)=152
152 % 10 = 2
So 851370-20-2 is a valid CAS Registry Number.

851370-20-2SDS

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 2,2-Dimethyl-propionic acid (2R,3S)-4-{(R)-6-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-2-[3-(4-methoxy-benzyloxy)-propyl]-6-[(E)-2-((S)-toluene-4-sulfinyl)-vinyl]-5,6-dihydro-4H-pyran-3-yl}-2,3-dimethyl-butyl ester

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 -
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More Details:851370-20-2 SDS

851370-20-2Upstream product

851370-20-2Relevant academic research and scientific papers

An approach to the imine ring system of pinnatoxins

Pelc, Matthew J.,Zakarian, Armen

, p. 1629 - 1631 (2007/10/03)

(Chemical Equation Presented) A concise stereoselective approach to the spirobicyclic imine fragment of pinnatoxins and pteriatoxins is described. The approach relies on a tandem reaction sequence involving consecutive sigmatropic rearrangements to build

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