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1,3-Dioxane, 2-(3-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5663-26-3

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5663-26-3 Usage

Structure

Nitro-substituted aromatic compound with a dioxane ring

Usage

Production of various chemical products and pharmaceuticals

Carcinogenicity

Group 2B carcinogen (IARC classification)

Health effects

Linked to adverse health effects, including potential risks to the reproductive and developmental systems

Safety

Handle and use with caution, follow proper safety protocols to minimize potential health hazards

Check Digit Verification of cas no

The CAS Registry Mumber 5663-26-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,6 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5663-26:
(6*5)+(5*6)+(4*6)+(3*3)+(2*2)+(1*6)=103
103 % 10 = 3
So 5663-26-3 is a valid CAS Registry Number.

5663-26-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-nitrophenyl)-1,3-dioxane

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:5663-26-3 SDS

5663-26-3Downstream Products

5663-26-3Relevant academic research and scientific papers

Highly efficient and chemoselective acetalization of carbonyl compounds catalyzed by new and reusab e zirconyl triflate, zr0(0tf)2

Moghadam, Majid,Mohammadpoor-Baltork, Iraj,Tangestaninejad, Shahram,Mirkhani, Valiollah,Yazdani, Parvin,Ghorjipoor, Saeedeh

experimental part, p. 131 - 135 (2009/09/30)

Various types of aromatic aldehydes were efficiently converted to their corresponding 1,3-dioxanes and 1,3-dioxolane with 1,3-propanediol and ethylene glycol, respectively, in the presence of catalytic amount of ZrO(OTf) 2 in acetonitrile at room temperature. The catalyst can be reused several times without loss of its catalytic activity. Very short reaction times, selective acetalization of aromatic aldehydes in the presence of aliphatic aldehydes and ketones, very mild reaction conditions, reusability of the catalyst, and easy workup are noteworthy advantages of this method.

Iodine-catalyzed, efficient and mild procedure for highly chemoselective acetalization of carbonyl compounds under neutral aprotic conditions

Karimi, Babak,Golshani, Behzad

, p. 784 - 788 (2007/10/03)

Various types of carbonyl compounds are efficiently converted to their 1,3-dioxanes by the use of 1,3-bis(trimethylsiloxy)propane (BTSP) and a catalytic amount of iodine (3-7 mol%) under essentially neutral aprotic condition.

ELECTRONIC EFFECT OF 1,3-DIOXACYCLANE SUBSTITUENTS IN NITROBENZALDEHYDE ACETALS

Ovchinnikov, V. V.,Evstaf'eva, Yu. G.,Latypova, V. Z.,Bogoveeva, G. A.,Cherkasov, R. A.

, p. 196 - 199 (2007/10/02)

The electronic effect of 1,3-dioxacyclane substituents in p- and m-nitrobenzaldehyde acetals was studied by IR spectroscopy and electrochemical reduction.In the investigated compounds the electron-withdrawing effect of the 1,3-dioxolane fragments is more

RADICAL-ANIONS GENERATED FROM CYCLIC ACETALS OF NITROBENZALDEHYDE, 2-NITRO-1,3-PROPANEDIOL, AND THEIR HETERO ANALOGS

Kukovitskii, D. M.,Zorin, V. V.,Zelechonok, Yu. B.,Zlot-skii, S. S.,Rakhmankulov, D. L.,Todres, Z. V.

, p. 132 - 136 (2007/10/02)

The potassium salts of the radical-anions of 2-nitrophenyl-1,3-diheterocycloalkanes and 5-alkyl-5-nitro-1,3-diheterocycloalkanes were generated in the liquid phase.The ESR spectra of the radical anions were analyzed, and it was concluded that the 1,3-dihe

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