Welcome to LookChem.com Sign In|Join Free

CAS

  • or

14852-31-4

Post Buying Request

14852-31-4 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

14852-31-4 Usage

Chemical Properties

white adhering fine powder

Uses

2-Hexadecanol is a volatile component and fatty alcohol identified in the petroleum ether extraction of leaves of Tecoma radicans.

Check Digit Verification of cas no

The CAS Registry Mumber 14852-31-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,8,5 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 14852-31:
(7*1)+(6*4)+(5*8)+(4*5)+(3*2)+(2*3)+(1*1)=104
104 % 10 = 4
So 14852-31-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H34O/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16(2)17/h16-17H,3-15H2,1-2H3

14852-31-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-HEXADECANOL

1.2 Other means of identification

Product number -
Other names Hexadecanol-2

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:14852-31-4 SDS

14852-31-4Relevant articles and documents

The question of remote steric effects

Menger,Nelson Jr., Kingsley H.

, p. 1347 - 1348 (1994)

Remote steric effects, thought to arise from long hydrocarbon chains coiling about reactive sites, are absent in three non-aqueous systems designed to maximize the effect.

Organoruthenium-supported polyoxotungstate - Synthesis, structure and oxidation of n-hexadecane with air

Meng, Rui-Qi,Wang, Bin,Sui, Hui-Min,Li, Bao,Song, Wei,Wu, Li-Xin,Zhao, Bing,Bi, Li-Hua

, p. 1935 - 1942 (2013)

A ruthenium complex, KNa[Ru2(C6H6) 2(CH3COO)6] (Ru-KNa), and its polyoxotungstate derivative, Na6[{Ru(C6H6)}2W 8O28(OH)2]·16H2O (Ru-Na), have been successfully isolated from routine synthetic reactions and characterized by X-ray single-crystal structure analysis, IR spectroscopy and elemental analysis. A remarkable aspect of Ru-KNa is that it has two ligand types, benzene and acetate, and the acetate ligands are connected exclusively by a central Na cation to form a dimeric sandwich-type structure, which is further connected by K cations to construct the 3D structures. Based on complex Ru-KNa, the compound Ru-Na was synthesized, and it consists of two {Ru(C 6H6)} units linked to a [W8O 28(OH)2]10- fragment by three Ru-O(W) bonds to result in an assembly with idealized C2 symmetry in which the polyanions form 3D structures by the connection of Na chains. Subsequently, the compound Ru-Na was anchored on (3-aminopropyl)triethoxysilane (apts) modified SBA-15 to prepare the solid catalysts, which were characterized by powder XRD, N2 adsorption measurements and FTIR spectroscopy. Finally, the catalytic efficiency of Ru-Na was assessed in the oxidation of n-hexadecane with air without any additives and solvents. The results indicated that Ru-Na is a heterogeneous catalyst and exhibits higher catalytic activity than previously reported Ru-containing polyoxotungstates. Copyright

Effect of precursor on the catalytic properties of Ni2P/SiO2 in methyl palmitate hydrodeoxygenation

Shamanaev, Ivan V.,Deliy, Irina V.,Aleksandrov, Pavel V.,Gerasimov, Evgeny Yu.,Pakharukova, Vera P.,Kodenev, Evgeny G.,Ayupov, Artem B.,Andreev, Andrey S.,Lapina, Olga B.,Bukhtiyarova, Galina A.

, p. 30372 - 30383 (2017/02/23)

The effect of phosphorus precursor on the physicochemical and catalytic properties of silica-supported nickel phosphide catalysts in the hydrodeoxygenation (HDO) of aliphatic model compound methyl palmitate (C15H31COOCH3) has been considered. Nickel aceta

A practical olefin hydroboration under liquid-liquid phase transfer catalysis conditions

Albanese, Domenico,Landini, Dario,Maia, Angelamaria,Penso, Michele

, p. 997 - 998 (2007/10/03)

The hydroboration of a series of representative olefins under LL-PTC conditions, followed by oxidative workup provides the corresponding alcohols in excellent yields and regio- and stereoselectivity.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 14852-31-4