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Benzylphosphonic acid ethyl p-nitrophenyl ester is a chemical compound with the molecular formula C14H14NO5P. It is a derivative of benzylphosphonic acid, featuring an ethyl group and a p-nitrophenyl ester functional group. This organic compound is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a key intermediate in the production of certain pesticides and other chemical compounds. Its structure allows for the formation of esters and other derivatives, making it a versatile building block in organic chemistry. The compound is characterized by its reactivity and stability, which are influenced by the presence of the nitro group on the phenyl ring, and it is often used in research and industrial settings for the development of new chemical entities.

3015-70-1

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3015-70-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3015-70-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,1 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3015-70:
(6*3)+(5*0)+(4*1)+(3*5)+(2*7)+(1*0)=51
51 % 10 = 1
So 3015-70-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H16NO5P/c1-2-20-22(19,12-13-6-4-3-5-7-13)21-15-10-8-14(9-11-15)16(17)18/h3-11H,2,12H2,1H3

3015-70-1SDS

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 1-[benzyl(ethoxy)phosphoryl]oxy-4-nitrobenzene

1.2 Other means of identification

Product number -
Other names ethyl 4-nitrophenyl benzylphosphonate

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:3015-70-1 SDS

3015-70-1Downstream Products

3015-70-1Relevant academic research and scientific papers

Direct Aryloxylation/Alkyloxylation of Dialkyl Phosphonates for the Synthesis of Mixed Phosphonates

Huang, Hai,Denne, Johanna,Yang, Chou-Hsun,Wang, Haobin,Kang, Jun Yong

, p. 6624 - 6628 (2018/05/14)

A strategy for the direct functionalization strategy of inertial dialkyl phosphonates with hydroxy compounds to afford diverse mixed phosphonates with good yields and functional-group tolerance has been developed. Mechanistic investigations involving both NMR studies and DFT studies suggest that an unprecedented highly reactive PV species (phosphoryl pyridin-1-ium salt), a key intermediate for this new synthetic transformation, is generated in situ from dialkyl phosphonate in the presence of Tf2O/pyridine.

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