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89723-54-6

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89723-54-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89723-54-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,2 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89723-54:
(7*8)+(6*9)+(5*7)+(4*2)+(3*3)+(2*5)+(1*4)=176
176 % 10 = 6
So 89723-54-6 is a valid CAS Registry Number.

89723-54-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name hex-1-en-1-one

1.2 Other means of identification

Product number -
Other names 1-Hexen-1-one

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:89723-54-6 SDS

89723-54-6Downstream Products

89723-54-6Relevant articles and documents

Oxygen bridged Homobinuclear Mn(II) compounds with Anthranilic acid: Theoretical calculations, oxidation and catalase activity

Su, Esra,Guven, Alaettin,Kani, Ibrahim

, (2018/02/07)

Two new homobinuclear manganese compounds with mixed ligands, [Mn2(μ1,1–2-NH2C6H4COO)2(phen)4](ClO4)2(CH3OH) (1), and [Mn2(μ1,3–2-NH2C6H4COO)2(bipy)4](ClO4)2 (2) (NH2C6H4COOH?=?anthranilic acid, bipy?=?2,2′-bipyridine, phen?=?1,10- phenanthroline) were synthesized and thoroughly characterized by elemental analysis, IR, UV and single crystal X-ray crystallography. X-ray structure analysis shows that in the mono- and bidentate carboxylate bridged compounds, Mn–Mn distances of 1 and 2 are 3,461??, and 4,639??, respectively. The energy of the compounds was determined with a DFT (Density Functional Theory) calculation on B3LYP/6-31G(d,p) optimized geometry by using the B3LYP/6-31G(d,p) basis set. These compounds acts as biomimetic catalyst and show catalase-like activity for the hydrogen peroxide dismutation at room temperature in different solvents with remarkable activity (TOF, Turnover frequency?=?mol of subst./(mol of cat. × time)) up to 12640?h?1 with 1, and 17910?h?1 with 2 in Tris–HCl buffer). Moreover, the catalytic activity of 1 and 2 has been studied for oxidation of alcohols (cinnamyl alcohol, benzyl alcohol, cyclohexanol, 1-octanol and 1-heptanol) and alkenes (cyclohexene, styrene, ethyl benzene, 1-octene and 1-hexene) in a homogeneous catalytic system consisting t-butylhydroperoxide (TBHP) as an oxidant in acetonitrile. Both compounds exhibited very high activity in the oxidation of cyclohexene to cyclohexanone (~80% selectivity, ~99% conversion in 1?h, TOF?=?243?h?1 and 226?h?1) and cinnamyl alcohol to cinnamaldehyde (~64% selectivity) as the main product with very high TOF value (9180?h?1 and 13040?h?1 in the first minute of reaction) (~100% conversion in 0.5?h) with TBHP at 70?°C in acetonitrile, for 1 and 2, respectively.

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