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16165-72-3

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16165-72-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16165-72-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,6 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16165-72:
(7*1)+(6*6)+(5*1)+(4*6)+(3*5)+(2*7)+(1*2)=103
103 % 10 = 3
So 16165-72-3 is a valid CAS Registry Number.

16165-72-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Diethyl-n-Octadecylphosphonate, 98 %

1.2 Other means of identification

Product number -
Other names Octadecyl-phosphonsaeure-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:16165-72-3 SDS

16165-72-3Downstream Products

16165-72-3Relevant articles and documents

High yield synthesis of some phosphonic acid derivatives as surface tethers for energy harvesting technologies

Mungalimane, Amshumali

, p. 143 - 148 (2014)

Efficient synthesis of novel 6-(2-bromo-2-methyl propanoyloxy)hexyl phosphonic acid, dodecane di-phosphonic acid, 6-(thiophene-3-carbonyloxy)hexyl phosphonic acid, octadecyl phosphonic acid and such other derivatives are reported here. These derivatives have a potential application as tethers to nanoparticle surfaces that can promote efficient electron transfer process in solar energy conversion.

Synthesis and structural study of long-chain hydrocarbon alkylphosphonic acids

Gaboyard,Hervaud,Boutevin

, p. 877 - 891 (2007/10/03)

Long-chain dialkyl alkylphosphonates were synthesized by radical addition of dialkyl hydrogenphosphonates onto alkenes in presence of di(t-butyl) peroxide. This synthetic route leads to high yields between 94 and 97%. We performed chemical modifications of these phosphonates in order to obtain acidic derivatives. The structure of these compounds was characterized by NMR analyses and mass spectroscopy. We also studied their thermal behaviour and various crystalline phases were put in evidence by differential scanning calorimetry and optical microscopy. The thermal stability of these compounds was compared by thermogravimetric analyses.

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