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5-Methylpentadecane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25117-33-3

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25117-33-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25117-33-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,1 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 25117-33:
(7*2)+(6*5)+(5*1)+(4*1)+(3*7)+(2*3)+(1*3)=83
83 % 10 = 3
So 25117-33-3 is a valid CAS Registry Number.
InChI:InChI=1/C16H34/c1-4-6-8-9-10-11-12-13-15-16(3)14-7-5-2/h16H,4-15H2,1-3H3

25117-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-methylpentadecane

1.2 Other means of identification

Product number -
Other names Pentadecane,5-methyl

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:25117-33-3 SDS

25117-33-3Downstream Products

25117-33-3Relevant academic research and scientific papers

Pd/SAPO-41 Bifunctional Catalysts with Enhanced Pd Dispersion Prepared by Ultrasonic-Assisted Impregnation: High Selectivity for n-Hexadecane Hydroisomerization

Bai, Xuefeng,Guo, Chunmu,Jia, Guozhi,Li, Tong,Maximov, A. L.,Su, Xiaofang,Wang, Wei,Wei, Xiaomeng,Wu, Wei

, p. 502 - 511 (2020/05/29)

Two series of Pd/SAPO-41 bifunctional catalysts were synthesized via the ultrasonic-assisted impregnation (xPd/S41-U) with different treating time and conventional incipient wetness impregnation methods (0.30Pd/S41-I) on the SAPO-41 molecular sieve, respe

Cobalt-catalyzed cross-coupling reaction between functionalized primary and secondary alkyl halides and aliphatic Grignard reagents

Cahiez, Gerard,Chaboche, Christophe,Duplais, Christophe,Giulliani, Arianna,Moyeux, Alban

scheme or table, p. 1484 - 1488 (2009/07/01)

The coupling of primary and secondary unactivated alkyl bromides with alkyl-Grignard reagents was performed in good yields under mild conditions by using a new catalytic system: consisting of cobalt chloride and tetramethylethylenediamine (CoCl2·2 LiI, 4TMEDA). The reaction is very chemoselective since ketone, ester and nitrile functions are tolerated.

Radical deoxygenation of tertiary alcohols via trifluoroacetates

Kim, Joong-Gon,Cho, Dae Hyan,Jang, Doo Ok

, p. 3031 - 3033 (2007/10/03)

Trifluoroacetates of tertiary alcohols undergo deoxygenation by Ph 2SiH2 in the presence of (tBuO)2 in excellent yields of the deoxy products without affecting the stereochemistry at β-carbon.

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