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Propanal, 2,2-dimethyl-3-[[(4-methylphenyl)sulfonyl]oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18516-19-3

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18516-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18516-19-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,5,1 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 18516-19:
(7*1)+(6*8)+(5*5)+(4*1)+(3*6)+(2*1)+(1*9)=113
113 % 10 = 3
So 18516-19-3 is a valid CAS Registry Number.

18516-19-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,2-dimethyl-3-oxopropyl) 4-methylbenzenesulfonate

1.2 Other means of identification

Product number -
Other names 2,2-dimethyl-3-tosyloxypropanal

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:18516-19-3 SDS

18516-19-3Relevant academic research and scientific papers

Chemistry of Four-Membered Cyclic Nitrones. 5. Synthesis and Oxidation of 1-Hydroxyazetidines

Pennings, Marcel L. M.,Reinhoudt, David N.

, p. 4043 - 4048 (2007/10/02)

1-(Benzyloxy)azetidines 9 are prepared by reductive cyclization of the corresponding O-benzyl oximes (6) that have a leaving group at the β-position.Reduction of the unprotected oxime 6a with sodium cyanoborohydride in acetic acid affords 3,4,4-trimethyli

SYNTHESIS OF 1-HYDROXYAZETIDINES AND THEIR CONVERSION INTO 1,4-DIACETOXY-2-AZETIDINONES

Pennings, M.L.M.,Kuiper, D.,Reinhoudt, D.N.

, p. 825 - 828 (2007/10/02)

1-Hydroxyazetidines (5), prepared by reductive cyclization of O-benzyl-β-tosyloxy oximes 1 and subsequent debenzylation, can be oxidized selectively either to four-membered cyclic nitrones (6 and 7) or to 1,4-diacetoxy-2-azetidinones (9).

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