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10138-59-7

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10138-59-7 Usage

Synthesis Reference(s)

Chemical and Pharmaceutical Bulletin, 28, p. 262, 1980 DOI: 10.1248/cpb.28.262

Check Digit Verification of cas no

The CAS Registry Mumber 10138-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,3 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10138-59:
(7*1)+(6*0)+(5*1)+(4*3)+(3*8)+(2*5)+(1*9)=67
67 % 10 = 7
So 10138-59-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H20O4/c1-3-15-11(13)9-7-5-6-8-10(9)12(14)16-4-2/h9-10H,3-8H2,1-2H3

10138-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl cyclohexane-1,2-dicarboxylate

1.2 Other means of identification

Product number -
Other names Cyclohexan-1,2-dicarbonsaeure-diaethylester

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:10138-59-7 SDS

10138-59-7Relevant articles and documents

CATALYTIC SYNTHESIS OF N-ALKYLOCTAHYDROISOINDOLES

Kozintsev, S. I.,Zhavrid, A. S.,Serzhanin, A. I.,Kozlov, N. S.

, p. 1346 - 1348 (1990)

Catalytic hydroamination of 1,2-bis(hydroxymethyl)cyclohexane by aliphatic nitriles over a nickel catalyst yielded a series of N-alkyl-substituted octahydroisoindoles.Conditions for their synthesis were selected.The IR, PMR, and mass spectra and the proba

Recyclable cobalt(0) nanoparticle catalysts for hydrogenations

Büschelberger, Philipp,Reyes-Rodriguez, Efrain,Sch?ttle, Christian,Treptow, Jens,Feldmann, Claus,Jacobi Von Wangelin, Axel,Wolf, Robert

, p. 2648 - 2653 (2018/05/30)

The search for new hydrogenation catalysts that replace noble metals is largely driven by sustainability concerns and the distinct mechanistic features of 3d transition metals. Several combinations of cobalt precursors and specific ligands in the presence of reductants or under high-thermal conditions were reported to provide active hydrogenation catalysts. This study reports a new method of preparation of small, monodisperse Co(0) nanoparticles (3-4 nm) from the reduction of commercial CoCl2 in the absence of ligands or surfactants. High catalytic activity was observed in hydrogenations of alkenes, alkynes, imines, and heteroarenes (2-20 bar H2). The magnetic properties enabled catalyst separation and multiple recyclings.

PROCESS FOR HYDROGENATION OF POLYCARBOXYLIC ACIDS OR DERIVATIVES THEROF

-

Paragraph 0041; 0042; 0043, (2013/06/27)

The disclosure provides a process for hydrogenation of polycarboxylic acids or derivatives thereof, including: hydrogenation of polycarboxylic acids or derivatives thereof in the presence of a catalyst, wherein the catalyst includes an active metal and a

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