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1067-88-5

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1067-88-5 Usage

General Description

Phosphonic acid, 1-propynyl-, diethyl ester, also known as propargylphosphonic acid diethyl ester, is a chemical compound derived from phosphonic acid and 1-propynyl. It is primarily used as a coupling agent and surface modifier in various industrial applications, including adhesives, coatings, and sealants. Phosphonic acid, 1-propynyl-, diethyl ester is known for its ability to improve adhesion and compatibility between different materials, making it valuable in enhancing the performance of various products. Additionally, it has potential applications in the synthesis of pharmaceuticals and agrochemicals. However, due to its potential hazards to human health and the environment, proper safety measures should be taken when handling and using this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 1067-88-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,6 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1067-88:
(6*1)+(5*0)+(4*6)+(3*7)+(2*8)+(1*8)=75
75 % 10 = 5
So 1067-88-5 is a valid CAS Registry Number.

1067-88-5SDS

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 1-diethoxyphosphorylprop-1-yne

1.2 Other means of identification

Product number -
Other names Prop-1-inyl-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:1067-88-5 SDS

1067-88-5Relevant articles and documents

Expanding the scope of Enantioselective FerroPHANE-promoted [3+2] annulations with α,β-unsaturated ketones

Pinto, Nathalie,Neel, Mathilde,Panossian, Armen,Retailleau, Pascal,Gilles Frison,Voituriez, Arnaud,Marinetti, Angela

scheme or table, p. 1033 - 1045 (2010/05/19)

The planar chiral 2-phospha [3]ferrocenophane I has been shown to be the first efficient nucleo- philic organocatalyst for the enantiose- lective synthesis of cyclopentenyl- phosphonates, through [3+2] cycliza- tions between diethyl allenylphospho- nate a

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