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32364-41-3

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32364-41-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32364-41-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,3,6 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 32364-41:
(7*3)+(6*2)+(5*3)+(4*6)+(3*4)+(2*4)+(1*1)=93
93 % 10 = 3
So 32364-41-3 is a valid CAS Registry Number.

32364-41-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethenylcyclopropan-1-ol,4-methylbenzenesulfonic acid

1.2 Other means of identification

Product number -
Other names 1-ethenyl-1-tosyloxycyclopropane

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:32364-41-3 SDS

32364-41-3Relevant articles and documents

Total Synthesis of Gelsemoxonine through a Spirocyclopropane Isoxazolidine Ring Contraction

Diethelm, Stefan,Carreira, Erick M.

supporting information, p. 6084 - 6096 (2015/05/27)

Plants of the species Gelsemium have found application in traditional Asian medicine for over a thousand years. Gelsemoxonine represents a novel constituent of this plant incorporating a highly functionalized azetidine at its core. We herein report a full

Versatile Synthesis of Enantiomerically Pure 2-Alkoxy-1-ethynylcyclopropanes and Their Application in the Synthesis of Enantiomerically Pure Bicyclo-oct-1-en-3-ones

Braese, Stefan,Schoemenauer, Sten,McGaffin, Gregory,Stolle, Andreas,Meijere, Armin de

, p. 545 - 555 (2007/10/03)

A variety of chiral, nonracemic 2-alkoxy-1-alkynylcylopropanes 7 were synthesized in good to very good yields from enantiomerically pure glycidol derivatives (glycidol tosylate, epichlorohydrin) by boron trifluoride promoted addition of lithium trimethyls

Palladium(0) catalyzed substitution reactions of cyclopropyl group containing allylic esters

Stolle, Andreas,Salauen, Jacques,De Meijere, Armin

, p. 4593 - 4596 (2007/10/02)

Complete regioselectivity is observed in palladium(0) catalyzed allylic substitution reactions of 1-vinylcyclopropyl 3 and cyclopropylldeneethyl esters 6 with a series of soft carbon nucleophiles to give γ-cyclopropylidene-1,3-dicarbonyl and 1-carbonyl-2-sulfonyl compounds. Highly functionalized mathylenecyclopropanes are thus obtained in good to excellent yields from easily accessible 1-vinylcyclopropyl tosylates 3d.

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