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dibutyl (1-hydroxycyclohexyl)phosphonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60324-12-1

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60324-12-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60324-12-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,3,2 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60324-12:
(7*6)+(6*0)+(5*3)+(4*2)+(3*4)+(2*1)+(1*2)=81
81 % 10 = 1
So 60324-12-1 is a valid CAS Registry Number.

60324-12-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-dibutoxyphosphorylcyclohexan-1-ol

1.2 Other means of identification

Product number -
Other names -

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:60324-12-1 SDS

60324-12-1Downstream Products

60324-12-1Relevant academic research and scientific papers

METHOD FOR PRODUCING PHOSPHONATE HAVING ALCOHOLIC HYDROXY GROUP

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Page/Page column 7; 9, (2008/06/13)

A novel process for preparing in a high purity and in a high yield phosphonates having a secondary and/or tertiary alcoholic hydroxyl group at the end of a P-C bond chain thereof with the use of a phosphite and a carbonyl compound as raw materials.

METHOD FOR PRODUCING PHOSPHORUS COMPOUND HAVING PHOSPHATE-PHOSPHONATE BOND

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Page/Page column 12; 16, (2008/06/13)

A novel process for preparing in a high purity and in a high yield phosphorus compounds having a phosphate-phosphonate bond within one molecule, along with only a small amount of a by-product, without being restricted by the kind of a phosphonate having an alcoholic hydroxyl group which is a raw material, without using a catalyst such as magnesium chloride, but only using a nitrogen-containing basic compound.

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