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81800-50-2

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81800-50-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81800-50-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,8,0 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 81800-50:
(7*8)+(6*1)+(5*8)+(4*0)+(3*0)+(2*5)+(1*0)=112
112 % 10 = 2
So 81800-50-2 is a valid CAS Registry Number.

81800-50-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,7,7-trimethylbicyclo[4.1.0]hept-3-en-5-one

1.2 Other means of identification

Product number -
Other names -

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:81800-50-2 SDS

81800-50-2Relevant articles and documents

Cobalt- and manganese-substituted ferrites as efficient single-site heterogeneous catalysts for aerobic oxidation of monoterpenic alkenes under solvent-free conditions

Menini, Luciano,Pereira, Marcio C.,Parreira, Luciana A.,Fabris, Jose D.,Gusevskaya, Elena V.

, p. 355 - 364 (2008/09/18)

Cobalt- and manganese-substituted ferrites were used as heterogeneous catalysts for liquid-phase aerobic oxidation of various monoterpenic alkenes. The materials were prepared by co-precipitation and characterized by Moessbauer spectroscopy, powder X-ray diffractometry, magnetization measurements, and elemental analysis. The results show that isomorphic substitution of iron in the ferrite crystalline structure occurred preferentially at octahedral positions and strongly affected its catalytic properties in the oxidation of monoterpenes. Various valuable oxygenated monoterpenic compounds were obtained with high combined selectivities (75-95%) at ca. 40% substrate conversions. Oxidations of β-pinene and 3-carene led almost exclusively to allylic mono-oxygenated derivatives, whereas limonene and α-pinene gave both epoxides and allylic products. The use of inexpensive catalyst and oxidant, solvent-free conditions, and high final product concentrations (ca. 40 wt%) are significant practical advantages of this environmentally friendly process. The catalysts undergo no metal leaching and can be easily recovered by the application of an external magnet and reused.

PRODUCTS OF THE CATALYTIC LIQUID-PHASE OXIDATION OF 3-CARENE

Vyglazov, O. G.,Manukov, E. N.,Fedorishcheva, M. N.,Ariko, N. G.,Chuiko, V. A.,Bazhina, G. N.

, p. 283 - 287 (2007/10/02)

The liquid-phase oxidation of 3-carene in the presence of various catalytic systems has been studied.The possibility has been shown of the directed preparation of 3-carene oxide, of ketones with a carane skeleton and a 7-membered ring, or of aromatic tertiary alcohols.

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