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128893-72-1

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128893-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128893-72-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,8,9 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 128893-72:
(8*1)+(7*2)+(6*8)+(5*8)+(4*9)+(3*3)+(2*7)+(1*2)=171
171 % 10 = 1
So 128893-72-1 is a valid CAS Registry Number.

128893-72-1SDS

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 diethyl [(3,5-di-tert-butyl-4-oxocyclohexa-2,5-dien-1-ylidene)methyl]phosphonate

1.2 Other means of identification

Product number -
Other names Diethyl 3,5-di-tert-butyl-4-oxo-2,5-cyclohexadienylidenemethylphosphonate

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:128893-72-1 SDS

128893-72-1Relevant articles and documents

7-substituted quinone methides as inhibitors for unsaturated monomers

-

, (2008/06/13)

Ethylenically unsaturated monomers are protected from premature polymerization during manufacture and storage by the incorporation therein of an effective stabilizing amount of a 7-substituted quinone methide compound.

α-SUBSTITUIERTE PHOSPHONATE 55. EIN NEUES TRIPHOSPHONAT AUS BISPHOSPHONO-CHINONMETHID UND DIALKYLPHOSPHIT

Gross, Hans,Ozegowski, Sigrid,Costisella, Burkhard

, p. 7 - 13 (2007/10/02)

By oxidation of 3,5-di-tert-butyl-4-hydroxyphenylmethanephosphonate (4) or the analogous arylsubstituted bisphosphonate (5) with PbO2 the hitherto unknown 7-mono- or 7.7-bisphosphonylated quinonemethides (13) or (11), resp., are formed in good yields.The quinonemethides simply added dialkylphosphite to form the bisphosphonate (5) or the trisphosphonate (13), the latter having a remarkable stability.The structures of the quinonemethides (13) and (11) as well as of the tris-phosphonate (12) could be proved unambiguously by IR-, 1H-, 13C- and 31P-NMR spectra.

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