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1001208-20-3

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1001208-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1001208-20-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,1,2,0 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1001208-20:
(9*1)+(8*0)+(7*0)+(6*1)+(5*2)+(4*0)+(3*8)+(2*2)+(1*0)=53
53 % 10 = 3
So 1001208-20-3 is a valid CAS Registry Number.

1001208-20-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ((1R,6S)-4-((tert-butyldimethylsilyl)oxy)-2-((2R,5R)-2,5-diphenylpyrrolidin-1-yl)-6-methylcyclohex-3-en-1-yl)methanol

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:1001208-20-3 SDS

1001208-20-3Upstream product

1001208-20-3Downstream Products

1001208-20-3Relevant academic research and scientific papers

Evolution of the total synthesis of (-)-Okilactomycin exploiting a tandem oxy-cope rearrangement/oxidation, a petasis-ferrier union/rearrangement, and ring-closing metathesis

Smith, Amos B. III,Bosanac, Todd,Basu, Kallol

supporting information; experimental part, p. 2348 - 2358 (2009/07/30)

An effective, asymmetric total synthesis of the antitumor antibiotic (-)-okilactomycin (1), as well as assignment of the absolute configuration,has been achieved exploiting a convergent strategy. Highlights of the s ynthesis include a diastereoselective o

Total synthesis of (-)-okilactomycin

Smith III, Amos B.,Basu, Kallol,Bosanac, Todd

, p. 14872 - 14874 (2008/09/20)

A highly convergent synthesis of (-)-okilactomycin is described. Key reactions of this synthesis include a strategy-level diastereoselective oxy-Cope rearrangement/oxidation sequence, a Petasis-Ferrier union/rearrangement tactic, and an efficient RCM reac

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