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14053-20-4

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14053-20-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14053-20-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,5 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14053-20:
(7*1)+(6*4)+(5*0)+(4*5)+(3*3)+(2*2)+(1*0)=64
64 % 10 = 4
So 14053-20-4 is a valid CAS Registry Number.

14053-20-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-ethyloxymethyl-2,2,7,8-tetramethyl-chroman-6-ol

1.2 Other means of identification

Product number -
Other names 5-ethoxymethyl-2,2,7,8-tetramethyl-chroman-6-ol

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:14053-20-4 SDS

14053-20-4Downstream Products

14053-20-4Relevant articles and documents

Oxidations of Vitamin E (α-Tocopherol) and Its Model Compound 2,2,5,7,8-Pentamethyl-6-hydroxychroman. A New Dimer

Suarna, Cacang,Craig, Donald C.,Cross, Keith J.,Southwell-Keely, Peter T.

, p. 1281 - 1284 (2007/10/02)

Oxidation of α-tocopherol (1a) with tert-butyl hydroperoxide in reagent-grade chloroform gave a new dimeric product which appeared to be both aromatic quinonoid.Repetition of the reaction with the tocopherol model compound 2,2,5,7,8-pentamethyl-6-hydroxychroman (1b) gave the corresponding dimer in high yield (30percent).This product was shown by two-dimensional, long-range proton-carbon correlation NMR spectra and subsequently by X-ray diffraction to be 2,3-dihydro-3,3,5,6,9,10,11a(R)-heptamethyl-7a(S)-(3-hydroxy-3-methylbutyl)-1H-pyranoxanthene-8(7aH),11(11aH)-dione (16b).It appeared to be formed by Diels-Alder addition of the intermediate quinone methide 7b to 2-(3-hydroxy-3-methylbutyl)-3,5,6-trimethylbenzo-1,4-quinone (14b), a known product of oxidation.

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