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1517-15-3

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1517-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1517-15-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,1 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1517-15:
(6*1)+(5*5)+(4*1)+(3*7)+(2*1)+(1*5)=63
63 % 10 = 3
So 1517-15-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H8O/c1-4-2-3-5(4)6/h4H,2-3H2,1H3

1517-15-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylcyclobutan-1-one

1.2 Other means of identification

Product number -
Other names 2-Methyl-cyclobutanon

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:1517-15-3 SDS

1517-15-3Relevant articles and documents

The first synthesis of spirocyclic sulfates from tertiary cyclopropanols and their reaction with normant homocuprates

Shklyaruck, Denis G.,Fedarkevich, Artsiom N.,Kozyrkov, Yurii Yu.

, p. 1855 - 1858 (2014)

Spirocyclic sulfates of 2- and 3-(hydroxyalkyl)cyclopropanols, obtainable through the Kulinkovich reaction from β-and γ-hydroxy carboxylic acid esters, respectively, were synthesized for the first time. The possibility of regio- and stereoselective alkyla

Howton,Buchman

, p. 4011 (1956)

Selective α-Methylation of Ketones

Frolov, Andriy I.,Ostapchuk, Eugeniy N.,Pashenko, Alexander E.,Chuchvera, Yaroslav O.,Rusanov, Eduard B.,Volochnyuk, Dmitriy M.,Ryabukhin, Sergey V.

, p. 7333 - 7346 (2021/06/28)

The convenient and scalable preparative approach for the two-step α-methylation of ketones is described. The optimized protocols for regioselective preparation of enaminones with further diastereoselective and functional groups tolerant hydrogenation to α-methylketones are developed. The scope and limitations of the proposed methodology are discussed. The advantages compared to known procedures are demonstrated. The unexpected role of acetone in the hydrogenation is suggested. The evaluation of the method for both early building block synthesis and late-stage CH-functionalization is shown. The elaborate procedures' preparability and scalability are demonstrated by the synthesis of several α-methyl ketones up to 100 g amount.

Pulling the levers of photophysics: How structure controls the rate of energy dissipation

Kuhlman, Thomas S.,Pittelkow, Michael,Solling, Theis I.,Moller, Klaus B.

supporting information, p. 2247 - 2250 (2013/03/28)

Internal conversion: The energy difference between the Franck-Condon and equilibrium geometries and the vibrational frequency of one or a few modes determine the relative importance of adiabatic and nonadiabatic dynamics and thus the rate of electronic en

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