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70158-20-2

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70158-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70158-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,1,5 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 70158-20:
(7*7)+(6*0)+(5*1)+(4*5)+(3*8)+(2*2)+(1*0)=102
102 % 10 = 2
So 70158-20-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H24O3/c1-4-6-7-12(5-2)10-16-13(15)9-8-11(3)14/h12H,4-10H2,1-3H3

70158-20-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethylhexyl 4-oxopentanoate

1.2 Other means of identification

Product number -
Other names levulinic acid-(2-ethyl-hexyl ester)

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:70158-20-2 SDS

70158-20-2Downstream Products

70158-20-2Relevant articles and documents

Inexpensive and tuneable protic ionic liquids based on sulfuric acid for the biphasic synthesis of alkyl levulinates

Chrobok, Anna,Gillner, Danuta,Matuszek, Karolina,Przypis, Marta,Swad?ba-Kwa?ny, Ma?gorzata

, (2020/04/23)

Alkyl levulinates are bio-derived chemicals, increasingly popular for their uses as solvents, additives and intermediates. However, efficient and recyclable catalysts for their synthesis are still the subject of intensive research. In this study, a wide range of alkyl levulinates was synthesized under mild conditions (room temperature, atmospheric pressure), using inexpensive and efficient Br?nsted acidic ionic liquids (ILs) based on sulfuric acid and off-the-shelf bases. Acidity of the ILs was closely related to their activity. The ILs could be easy separated and recycled, without significant changes in conversion or selectivity over 10 cycles (yields ca. 90–95%). Under optimized conditions, a 99% yield of pentyl levulinate (model reaction) was achieved. The method was demonstrated to be efficient in the synthesis of levulinates of C1-C16 linear, branched and cyclic alcohols. This innovative, green route to alkyl levulinates fits well within the sustainable development strategy.

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