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1002-17-1

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1002-17-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1002-17-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1002-17:
(6*1)+(5*0)+(4*0)+(3*2)+(2*1)+(1*7)=21
21 % 10 = 1
So 1002-17-1 is a valid CAS Registry Number.
InChI:InChI=1S/C12H26/c1-11(2)9-7-5-6-8-10-12(3)4/h11-12H,5-10H2,1-4H3

1002-17-1SDS

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 2,9-dimethyldecane

1.2 Other means of identification

Product number -
Other names 2,5-PYRAZINEDIAMINE

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:1002-17-1 SDS

1002-17-1Downstream Products

1002-17-1Relevant articles and documents

Electrochemical cross-coupling of biogenic di-acids for sustainable fuel production

Holzh?user, F. Joschka,Creusen, Guido,Moos, Gilles,Dahmen, Manuel,K?nig, Andrea,Artz, Jens,Palkovits, Stefan,Palkovits, Regina

, p. 2334 - 2344 (2019/05/21)

Direct electrocatalytic conversion of bio-derivable acids represents a promising technique for the production of value-added chemicals and tailor-made fuels from lignocellulosic biomass. In the present contribution, we report the electrochemical decarboxylation and cross-coupling of ethyl hydrogen succinate, methyl hydrogen methylsuccinate and methylhexanoic acid with isovaleric acid. The reactions were performed in aqueous solutions or methanol at ambient temperatures, following the principles of green chemistry. High conversions of the starting materials have been obtained with maximum yields between 42 and 61% towards the desired branched alkane products. Besides costly Pt electrodes also (RuxTi1-x)O2 on Ti electrodes exhibited a notable activity for cross-Kolbe electrolysis. As some of the products are insoluble in water, easy product isolation and reuse of the reaction solvent is enabled via phase separation. Several side products have been identified to evaluate the efficiency of the reaction and to elucidate the factors influencing the product selectivity. The yielded alkanes and esters were assessed with regard to their potential as fuels for internal combustion engines. While the longer alkanes constitute promising candidates for the compression-ignition engine, the smaller ester represents an interesting option for the spark-ignition engine.

Coupling Reaction of Grignard Reagents with α,ω-Dibromoalkanes in the Presence of Copper(I) Bromide-HMPA: Preparation of α,ω-Bis(vinylaryl)alkanes

Nishimura, Jun,Yamada, Noriyuki,Horiuchi, Yuzuru,Ueda, Eiji,Ohbayashi, Akihiro,Oku, Akira

, p. 2035 - 2037 (2007/10/02)

The coupling reaction of Grignard reagents with α,ω-dibromoalkanes took place smoothly in THF/HMPA (12:1) in the presence of a catalytic amount of copper(I) bromide and gave the products in 60-100 percent yields.Several α,ω-bis(vinylaryl)alkanes were prepared in reasonable yields by the application of this reaction.

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