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930-56-3

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930-56-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 930-56-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 0 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 930-56:
(5*9)+(4*3)+(3*0)+(2*5)+(1*6)=73
73 % 10 = 3
So 930-56-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O/c1-4-3-6(4)5(2)7/h4,6H,3H2,1-2H3

930-56-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-methylcyclopropyl)ethanone

1.2 Other means of identification

Product number -
Other names Ketone,methyl 2-methylcyclopropyl

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:930-56-3 SDS

930-56-3Relevant articles and documents

Quantitative production of butenes from biomass-derived γ-valerolactone catalysed by hetero-atomic MFI zeolite

Lin, Longfei,Sheveleva, Alena M.,da Silva, Ivan,Parlett, Christopher M. A.,Tang, Zhimou,Liu, Yueming,Fan, Mengtian,Han, Xue,Carter, Joseph H.,Tuna, Floriana,McInnes, Eric J. L.,Cheng, Yongqiang,Daemen, Luke L.,Rudi?, Svemir,Ramirez-Cuesta, Anibal J.,Tang, Chiu C.,Yang, Sihai

, p. 86 - 93 (2019/12/30)

The efficient production of light olefins from renewable biomass is a vital and challenging target to achieve future sustainable chemical processes. Here we report a hetero-atomic MFI-type zeolite (NbAlS-1), over which aqueous solutions of γ-valerolactone (GVL), obtained from biomass-derived carbohydrates, can be quantitatively converted into butenes with a yield of >99% at ambient pressure under continuous flow conditions. NbAlS-1 incorporates simultaneously niobium(v) and aluminium(iii) centres into the framework and thus has a desirable distribution of Lewis and Br?nsted acid sites with optimal strength. Synchrotron X-ray diffraction and absorption spectroscopy show that there is cooperativity between Nb(v) and the Br?nsted acid sites on the confined adsorption of GVL, whereas the catalytic mechanism for the conversion of the confined GVL into butenes is revealed by in situ inelastic neutron scattering, coupled with modelling. This study offers a prospect for the sustainable production of butene as a platform chemical for the manufacture of renewable materials.

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