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14744-18-4

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14744-18-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14744-18-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,4 and 4 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14744-18:
(7*1)+(6*4)+(5*7)+(4*4)+(3*4)+(2*1)+(1*8)=104
104 % 10 = 4
So 14744-18-4 is a valid CAS Registry Number.

14744-18-4SDS

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 2,2,5,5-tetramethyloxolane-3,4-dione

1.2 Other means of identification

Product number -
Other names 2,2,5,5-tetramethyl-furan-3,4-dione

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:14744-18-4 SDS

14744-18-4Relevant articles and documents

Crystal and Molecular Structure and Spectra of 2',2',5,5,5',5',7,7-Octamethyl-2',5,5',7-tetrahydrofuro-1-oxa-3,4-diselenin-2-spiro-3'-furan-4'(3'H)-one from Selenium Dioxide Oxidation of 2,2,5,5-Tetramethyltetrahydrofuran-3-one. A Novel Six-membered Heterocyclic Ring System in ...

Kuronen, Pirjo,Laitalainen, Tarja,Orama, Olli

, p. 961 - 966 (2007/10/02)

When 2,2,5,5-tetramethyltetrahydrofuran-3-one 1 was oxidized with selenium dioxide in ethanol, the title heterocycle 4 was formed along with 2,2,5,5-tetramethyltetrahydro-3,4-furandione 2.The diselenide 4 represents a novel six-membered heterocycle in the chalcogen series.

SYNTHESIS AND STRUCTURE OF E,Z-ISOMERIC FIVE-MEMBERED CYCLIC α-KETO-N-METHYL NITRONES

Rodina, L. L.,Kuruts, I.,Korobitsyna, I. K.

, p. 1711 - 1722 (2007/10/02)

The respective E-isomeric nitrones were obtained by methylation of the monooximes of cyclic α-diketones.The photochemical transformation of five-membered cyclic E-α-keto-N-methyl nitrones into the thermodynamically less stable Z isomers was realized for the first time, and the conditions for the preparative realization of the process were determined.Detailed investigation of the IR, UV, PMR and 13C NMR spectra and the dipole moments of the obtained nitrones showed that the dipole moments and PMR spectra are most suitable for determinig the configuration (E or Z).

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