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3-Octene-2,7-dione, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81056-91-9

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81056-91-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81056-91-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,0,5 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 81056-91:
(7*8)+(6*1)+(5*0)+(4*5)+(3*6)+(2*9)+(1*1)=119
119 % 10 = 9
So 81056-91-9 is a valid CAS Registry Number.

81056-91-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-2-octene-2,7-dione

1.2 Other means of identification

Product number -
Other names 3E-octen-2,7-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:81056-91-9 SDS

81056-91-9Upstream product

81056-91-9Downstream Products

81056-91-9Relevant academic research and scientific papers

A NEW SYNTHESIS OF β-NITRO CARBONYL COMPOUNDS FROM ALKYL VINYL KETONES WITH SODIUM NITRITE-ACETIC ACID IN TETRAHYDROFURAN

Miyakoshi, Tetuo,Saito, Shojiro,Kumanotani, Ju

, p. 1677 - 1678 (1981)

The reaction of alkyl vinyl ketones with sodium nitrite-acetic acid in THF gave the corresponding β-nitro carbonyl compounds in 42-82percent yield.

"Head-to-head" dimerization and dehydrodimerization of vinyl ketones catalyzed by modified rhodium(I) complexes

Kovalev, I. P.,Kolmogorov, Yu. N.,Strelenko, Yu. A.,Ignatenko, A. V.,Vinogradov, M. G.,Nikishin, G. I.

, p. 125 - 133 (2007/10/02)

The dimerization of vinyl ketones RC(O)CH=CH2, I (R = Me, tBu, Ph, p-MeC6H4, cyclopropyl, 2-(5-methylfuryl)) at 80 deg C in the presence of the catalytic system 2-MCl2 leads preferably to either α,β-unsaturated 1,6-diketones RC(O)C

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