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7413-09-4

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7413-09-4 Usage

General Description

Phosphonic acid, cyclohexyl-, diethyl ester is a chemical compound with the formula C10H21O3P. It is a colorless liquid with a fruity odor, and is commonly used as a corrosion inhibitor in industrial applications. Phosphonic acid, cyclohexyl-, diethyl ester is stable under normal temperatures and pressures, and is not considered to be highly flammable or reactive. It is also used as a lubricant additive to improve the anti-wear and extreme pressure performance of lubricants. Phosphonic acid, cyclohexyl-, diethyl ester is classified as a low hazard chemical, but proper handling and storage procedures should still be followed to minimize any potential risks.

Check Digit Verification of cas no

The CAS Registry Mumber 7413-09-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,1 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7413-09:
(6*7)+(5*4)+(4*1)+(3*3)+(2*0)+(1*9)=84
84 % 10 = 4
So 7413-09-4 is a valid CAS Registry Number.

7413-09-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name diethoxyphosphorylcyclohexane

1.2 Other means of identification

Product number -
Other names cyclohexyl-phosphonic acid diethyl ester

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:7413-09-4 SDS

7413-09-4Relevant articles and documents

Hydrophosphonylation of alkenes or nitriles by double radical transfer mediated by titanocene/propylene oxide

Midrier, Camille,Lantsoght, Mathias,Volle, Jean-No?l,Pirat, Jean-Luc,Virieux, David,Stevens, Christian V.

scheme or table, p. 6693 - 6696 (2012/01/04)

Hydrophosphonylation reactions have emerged as efficient processes for the functionalization of alkenes or alkynes. Synthesis of alkylphosphonates was achieved by an original double radical transfer mediated by titanocene and propylene oxide. By the same way, nitriles which are considered as inert functions in radical process lead to aminobisphosphonates.

Reactions of dialkyl phosphonates with hexacarbonylmolybdenum(0) and hexacarbonyltungsten(0). Structure of intermediates in the catalytic phosphorylation of alkenes

Kuramshin,Nikolaev,Cherkasov

, p. 1744 - 1749 (2007/10/03)

Reactions of dialkyl phosphonates with catalytic precursors in the phosphorylation of alkenes and aryl halides, homoligand molybdenum(0) and tungsten(0) carbonyl complexes, were studied by quantum-chemical and spectroscopic (IR and NMR) methods. Schemes w

Addition of dialkyl hydrogen phosphites to alkenes in the presence of carbonyl complexes of chromium subgroup metals and iron

Kuramshin,Kuramshina,Cherkasov

, p. 354 - 358 (2007/10/03)

Depending on the reactant ratio and order of their mixing, reactions of dialkyl hydrogen phosphite with alkenes in the presence of catalytic amounts of homoligand carbonyl complexes of iron or chromium subgroup metals yield phosphonates by two pathways: r

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