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2609-49-6

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2609-49-6 Usage

Chemical Properties

clear slightly viscous yellow-orange to dark red

Check Digit Verification of cas no

The CAS Registry Mumber 2609-49-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,0 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2609-49:
(6*2)+(5*6)+(4*0)+(3*9)+(2*4)+(1*9)=86
86 % 10 = 6
So 2609-49-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H16NO5P/c1-3-16-18(15,17-4-2)9-10-5-7-11(8-6-10)12(13)14/h5-8H,3-4,9H2,1-2H3

2609-49-6 Well-known Company Product Price

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  • TCI America

  • (D5208)  Diethyl (4-Nitrobenzyl)phosphonate  >97.0%(GC)

  • 2609-49-6

  • 5g

  • 1,100.00CNY

  • Detail

2609-49-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(diethoxyphosphorylmethyl)-4-nitrobenzene

1.2 Other means of identification

Product number -
Other names diethyl 4-nitrophenylmethanephosphonate

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:2609-49-6 SDS

2609-49-6Relevant articles and documents

Novel chiral bis-dipolar 6,6'-disubstituted binaphthol derivatives for second-order nonlinear optics: Synthesis and linear and nonlinear optical properties

Deussen,Hendrickx,Boutton,Krog,Clays,Bechgaard,Persoons,Bj?rnholm

, p. 6841 - 6852 (1996)

A number of thermally and optically stable, bis-dipolar chiral molecules based on two geometries of the binaphthol (BN) system with different acceptors/substituents have been synthesized for the first time, and the synthetic routes are reported: optically

From polynorbornene to the complementary polynorbornene by replication

Lin, Nai-Ti,Lin, Shu-Yi,Lee, Shern-Long,Chen, Chun-Hsien,Hsu, Chao-Hsiung,Hwang, Lian Pin,Xie, Zhen-Yu,Chen, Chung-Hsuan,Huang, Shou-Ling,Luh, Tien-Yau

, p. 4481 - 4485 (2007)

In undergoing a DNA-like replication process, the single-stranded polynorbornene acts as a template for norbornene monomer adhesion through ester linkages (see scheme). Polymerization of the adhered monomers affords the corresponding unsymmetric double-st

Visible-light-mediated phosphonylation reaction: formation of phosphonates from alkyl/arylhydrazines and trialkylphosphites using zinc phthalocyanine

Hosseini-Sarvari, Mona,Koohgard, Mehdi

, p. 5905 - 5911 (2021/07/12)

In this work, we developed a ligand- and base-free visible-light-mediated protocol for the photoredox syntheses of arylphosphonates and, for the first time, alkyl phosphonates. Zinc phthalocyanine-photocatalyzed Csp2-P and Csp3-P bond formations were efficiently achieved by reacting aryl/alkylhydrazines with trialkylphosphites in the presence of air serving as an abundant oxidant. The reaction conditions tolerated a wide variety of functional groups.

ANTIMALARIAL COMPOUNDS

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Page/Page column 36-38, (2020/10/20)

Antimalarial compounds of the formula: in which n is 1 or 2; X is C or N; R1 is a moiety comprising a secondary amine and a tertiary amine joined by a C2 to C4 alkyl chain; and R2 is CF3, F, or H, or an analog, combination, derivative, prodrug, stereoisomer, or pharmaceutically acceptable salt thereof. Pharmaceutical compounds including the antimalarial compounds. Methods of treating or preventing malaria comprising administering an effective amount of the antimalarial compounds.

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