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1069-83-6

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1069-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1069-83-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,6 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1069-83:
(6*1)+(5*0)+(4*6)+(3*9)+(2*8)+(1*3)=76
76 % 10 = 6
So 1069-83-6 is a valid CAS Registry Number.
InChI:InChI=1/4C2H5.2Al.O/c4*1-2;;;/h4*1H2,2H3;;;/rC8H20Al2O/c1-5-9(6-2)11-10(7-3)8-4/h5-8H2,1-4H3

1069-83-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name diethylalumanyloxy(diethyl)alumane

1.2 Other means of identification

Product number -
Other names Tetraaethyldialuminoxan

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:1069-83-6 SDS

1069-83-6Relevant articles and documents

Reactions of lanthanide acetylacetonates with triethylaluminum

Bulgakov,Kuleshov,Vafin,Ibragimov,Dzhemilev

, p. 299 - 304 (2008)

The reactions of lanthanide acetylacetonates Ln(acac)3· H2O (Ln = Nd, Tb, Ho, Lu) with Et3Al in toluene were studied by spectral methods (photoluminescence; taumetry; NMR, IR, and UV-vis spectroscopy) using GLC, volumetry,

Gavrilenko, V. V.,Chekulaeva, L. A.,Antonovich, V. A.,Zakharkin, L. I.

, (1980)

ORGANOMETALLIC REACTION MECHANISMS. XVIII. CONCERNING THE NATURE OF THE TRANSITION STATE IN THE REACTION OF TRIALKYLALUMINUM COMPOUNDS WITH KETONES

Ashby, E. C.,Smith, R. Scott

, p. 71 - 85 (2007/10/02)

Et2AlCH2AlEt2 (1) has been used as a mechanistic probe to determine the nature of the transition state in the reaction of two equivalents of a trialkylaluminum compound with a ketone in hydrocarbon solvent. 1 was prepared in benzene and the solution composition determined.Low temperature 1H NMR data of 1 as the mono(diethyl etherate) indicate that the ether oxygen is simultaneously coordinated to both aluminum atoms.The reactions of 1 with 4-t-butylcyclohexanone in hydrocarbon solvent were compared to the reactions of triethylaluminium with the same ketone.The results support the importance of a bridging alkyl group described by the formation of a six-centered transition state when two equivalents of a trialkylaluminum compound are allowed to react with a ketone in hydrocarbon solvent.The results also argue against a transition state described by two moles of trialkylaluminum compound complexed to the carbonyl oxygen atom.

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