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Phosphonisocyanatidic acid, methyl-, phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17848-02-1

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17848-02-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17848-02-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,4 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17848-02:
(7*1)+(6*7)+(5*8)+(4*4)+(3*8)+(2*0)+(1*2)=131
131 % 10 = 1
So 17848-02-1 is a valid CAS Registry Number.

17848-02-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [isocyanato(methyl)phosphoryl]oxybenzene

1.2 Other means of identification

Product number -
Other names phenyl isocyanatomethylphosphonate

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:17848-02-1 SDS

17848-02-1Relevant academic research and scientific papers

Catalytic synthesis of phosphoryl isocyanates

Goryunov,Molchanova,Goryunova,Baulina,Petrovskii,Mikhailovskaya,Buyanovskaya,Nifant'ev

, p. 2626 - 2628 (2005)

A general efficient method for the synthesis of phosphoryl isocyanates was developed. The method involves reactions of phosphoryl chlorides with sodium cyanate in the presence of anhydrous magnesium chloride as a catalyst.

N-Alkyl-N'-[(alkyl/aryl)(alkoxy/aroxy)phosphoryl]ureas: Synthesis and extraction properties toward f-elements

Goryunov,Baulina,Goryunova,Matveeva,Safiulina,Nifant'ev

, p. 141 - 148 (2014)

A reaction of chlorophosphonates R1R2P(O)Cl with NaOCN and subsequent treatment with octylamine lead to phosphorylureas R 1R2P(O)NHC(O)NHC8H17-n (R 1 = EtO, PhO; R2 = Me, Ph). Their extraction capability toward UVI and a number of tervalent lanthanides (LaIII, NdIII, HoIII, YbIII) was studied. Efficiency and selectivity of these ligands in the extraction of f-elements from nitric acid solutions to chloroform were compared with extraction properties of a model phosphine oxide-type phosphorylurea MePhP(O)NHC(O)NHC8H 17-n and carbamoylphosphine oxide Ph2P(O)CH 2C(O)NBu2.

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