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1552-41-6

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1552-41-6 Usage

General Description

(4-CYANOBENZYL)PHOSPHONIC ACID DIETHYL ESTER is a chemical compound with the molecular formula C14H17N2O3P. It is a diethyl ester derivative of (4-cyanobenzyl)phosphonic acid, which is a phosphonic acid with a cyanobenzyl group. (4-CYANOBENZYL)PHOSPHONIC ACID DIETHYL ESTER is commonly used as a precursor in organic synthesis and pharmaceutical research. It is also used as a building block in the production of certain pharmaceuticals and agrochemicals. Additionally, it exhibits potential biological activity and is being studied for its potential applications in medicine and technology. Due to its unique structure and properties, (4-CYANOBENZYL)PHOSPHONIC ACID DIETHYL ESTER is of interest to researchers and industries in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 1552-41-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,5 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1552-41:
(6*1)+(5*5)+(4*5)+(3*2)+(2*4)+(1*1)=66
66 % 10 = 6
So 1552-41-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H16NO3P/c1-3-15-17(14,16-4-2)10-12-7-5-11(9-13)6-8-12/h5-8H,3-4,10H2,1-2H3

1552-41-6 Well-known Company Product Price

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  • TCI America

  • (D3323)  Diethyl (4-Cyanobenzyl)phosphonate  >98.0%(GC)

  • 1552-41-6

  • 5g

  • 1,180.00CNY

  • Detail
  • TCI America

  • (D3323)  Diethyl (4-Cyanobenzyl)phosphonate  >98.0%(GC)

  • 1552-41-6

  • 25g

  • 3,850.00CNY

  • Detail

1552-41-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Diethyl (4-Cyanobenzyl)phosphonate

1.2 Other means of identification

Product number -
Other names (4-Cyanobenzyl)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:1552-41-6 SDS

1552-41-6Relevant articles and documents

N-alkylation of indole compounds in modified Wittig-Horner reaction

Singh, Anil K.,Asefa, Abera

, p. 1491 - 1494 (2007)

N-Ethyl-3-styrylindoles are prepared under modified Wittig-Horner reaction conditions. Copyright Taylor & Francis Group, LLC.

Self-assembly and luminescence of oligo(p-phenylene vinylene) amphiphiles

Hulvat, James F.,Sofos, Marina,Tajima, Keisuke,Stupp, Samuel I.

, p. 366 - 372 (2005)

We have synthesized a series of amphiphilic molecules consisting of oligo(phenylene vinylene) (OPV) asymmetrically end-substituted with a hydrophilic poly(ethylene glycol) (PEG) segment and a hydrophobic alkyl chain. This amphiphilic structure induces sel

Supramolecular metallacycles with a 'pseudo double-paracyclophane' structure based on flexible π-conjugated linkers

Shen,El Sayed Moussa,Yao,Lescop

, p. 11560 - 11563 (2015)

The straightforward synthesis of new supramolecular metallacycles having a 'pseudo double-paracyclophane' structure is presented. They are obtained from the reaction of a pre-assembled Cu(i) bimetallic precursor bearing short intermetallic distances with

Determination and application of the excited-state substituent constants of pyridyl and substituted phenyl groups

Cao, Chao-Tun,Yan, Lu,Cao, Chenzhong

, (2021/05/21)

Thirty six 1-pyridyl-2-arylethenes XCH=CHArY (abbreviated XAEY) were synthesized, in which, X is 2-pyridyl, 3-pyridyl and 4-pyridyl and Y is OMe, Me, H, Br, Cl, F, CF3, and CN. Their ultraviolet absorption spectra were measured in anhydrous ethanol, and their wavelengths of absorption maximum λmax were recorded. Also, the 234 λmax values of 1-substituted phenyl-2-arylethylene compounds (XAEY, where X is substituted phenyl) were collected. The excited-state substituent constants (Formula presented.) of three pyridyl groups and 23 substituted phenyl groups (total of 26) were obtained by means of curve-fitting method. Taking the λmax values of 358 samples of bi-arylethene derivatives as a data set and 126 samples of bi-aryl Schiff bases (including nine compounds synthesized by this work) as another data set, quantitative correlation analyses were performed by employing the obtained (Formula presented.) as a parameter, and good results were obtained for the two data sets. The reliability of the obtained (Formula presented.) values was verified. The results of this paper can provide excited-state substituent constants for the study and application of optical properties of conjugated organic compounds containing aryl groups.

OPTICAL DATA COMMUNICATION SYSTEM COMPRISING PARA-PHENYLENEVINYLENES AND SPECIFIC PARA-PHENYLENEVINYLENES

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Page/Page column 51; 52, (2020/01/08)

An optical data communication system comprising para-phenylenevinylenes, a receiver for an optical data communication system comprising para-phenylenevinylenes, a transmitter for an optical data communication system comprising para-phenylenevinylenes, the use of para- phenylenevinylenes in an optical data communication system, specific para-phenylenevinylenes and their preparation.

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