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1002-43-3

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1002-43-3 Usage

General Description

3-Methylundecane is a chemical compound belonging to the class of alkanes, specifically an alkane with 11 carbon atoms and a methyl group attached to the third carbon atom. It is a colorless, flammable liquid with a faint odor and is commonly used in the production of perfumes and fragrances due to its pleasant smell. It is also used as an intermediate in the synthesis of other organic compounds and as a solvent in various industrial processes. 3-Methylundecane has low solubility in water and is considered to have low toxicity, making it a relatively safe chemical for handling and use in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1002-43-3 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, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1002-43:
(6*1)+(5*0)+(4*0)+(3*2)+(2*4)+(1*3)=23
23 % 10 = 3
So 1002-43-3 is a valid CAS Registry Number.

1002-43-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-METHYLUNDECANE

1.2 Other means of identification

Product number -
Other names 3-Methylhendecane

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:1002-43-3 SDS

1002-43-3Downstream Products

1002-43-3Relevant articles and documents

Synthesis, characterization and isomerization performance of micro/mesoporous materials based on H-ZSM-22 zeolite

Liu, Suyao,Ren, Jie,Zhang, Huaike,Lv, Enjing,Yang, Yong,Li, Yong-Wang

, p. 11 - 23 (2016)

Micro/mesoporous materials with different mesoporosities were prepared through recrystallization of H-ZSM-22 zeolite in alkaline solution with cetyltrimethylammonium bromide template (CTAB). The structure, morphology, pore properties, acidity and isomerization performance of the catalysts by using the resulting materials were characterized and assessed. The dissolution and recrystallization procedure introduced the well-developed mesoporous structure of MCM-41 type with the meso-scale channels of about 3 nm in size on the outer surfaces of the microporous H-ZSM-22 zeolites, forming the micro/mesoporous materials, which possessed increased weak B acid sites at the pore mouths and a reduced amount of total acid sites. It is shown that the presence of well-developed mesopores could remarkably improve the selectivity to multi-branched products and suppress the side cracking reactions in n-dodecane isomerization. The micro/mesoporous Pt/ZSM-22/MCM-41 bifunctional catalyst with suitable recrystallization degree exhibits high isomerization selectivity under high conversion in long-chain n-alkane isomerization compared to the original microporous Pt/H-ZSM-22 catalyst.

Unusual pathway of the tantalum-catalyzed carboalumination reaction of alkenes with triethylaluminum

Sultanov, Rifkat M.,Samoilova, Elena V.,Popod'Ko, Natal'Ya R.,Tulyabaev, Artur R.,Sabirov, Denis Sh.,Dzhemilev, Usein M.

supporting information, p. 6619 - 6623 (2013/11/19)

Carboalumination of 1-alkenes (1-hexene, 1-octene, 1-decene) with Et 3Al in the presence of catalytic amounts of TaCl5 results in a mixture of 2-(R-substituted)- and 3-(R-substituted)-n-butylaluminums (1:1 ratio) in total yields of 75-85%. The TaCl5-catalyzed reaction of bicyclo[2.2.1]hept-2-ene, endo-tricyclo[5.2.1.02,6]deca-3,8-diene, and (exo/endo)-5-methylbicyclo[2.1.1]hept-2-ene with Et3Al leads to the formation of diethyl[2-exo-(2′-norbornylethyl)]aluminums in high yields. DFT calculations confirm the thermodynamic preference of the final exo product. The multistep reaction mechanisms for the formation of the resultant organoaluminums through tantalacyclopentanes as key intermediates are also discussed.

NEW REACTION OF α-OLEFINS WITH DIETHYLMAGNESIUM, CATALYZED BY Cp2ZrCl2

Dzhemilev, U. M.,Vostrikova, O. S.,Sultanov, R. M.

, p. 193 - 195 (2007/10/02)

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