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13042-46-1

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13042-46-1 Usage

General Description

1,3-Dioxan-5-amine, 2-phenyl-, cis-(9CI) is a chemical compound with the molecular formula C9H11NO2. It is a member of the amine class of organic compounds and is characterized by a dioxane ring with an amine group and a phenyl group attached. This chemical has potential applications in the pharmaceutical and agricultural industries and may be used as a building block in the synthesis of other organic compounds. However, it is important to note that 1,3-Dioxan-5-amine, 2-phenyl-, cis-(9CI) may have potential hazards associated with its handling and use, and appropriate precautions should be taken when working with this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 13042-46-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,4 and 2 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13042-46:
(7*1)+(6*3)+(5*0)+(4*4)+(3*2)+(2*4)+(1*6)=61
61 % 10 = 1
So 13042-46-1 is a valid CAS Registry Number.

13042-46-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-(2-phenyl-[1,3]dioxan-5-yl)-amine

1.2 Other means of identification

Product number -
Other names cis-(2-phenyl-1,3-dioxan-5-yl)amine

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:13042-46-1 SDS

13042-46-1Relevant articles and documents

Toward fullerene-based X-ray contrast agents: Design and synthesis of non-ionic, highly-iodinated derivatives of C60

Wharton, Tim,Wilson, Lon J

, p. 561 - 564 (2002)

An X-ray contrast agent precursor based on C60 has been designed, synthesized, and characterized. The compound is the monoadduct of a malonodiamide containing six iodine atoms and eight acetal-protected alcohols with multiple hindered rotations

Ammonium Chloride-Promoted Rapid Synthesis of Monosubstituted Ureas under Microwave Irradiation

Lan, Chunling Blue,Auclair, Karine

, p. 5135 - 5146 (2021/10/19)

Monosubstituted ureas are important scaffolds in organic chemistry. They appear in various biologically active compounds and serve as versatile precursors in synthesis. Monosubstituted ureas were originally prepared using toxic and hazardous phosgene equivalents. Modern methods include transamidation of urea and nucleophilic addition to cyanate salts, both of which suffer from a narrow substrate scope due to the need for a strong acid and prolonged reaction times. We hereby report that ammonium chloride can promote the reaction between amines and potassium cyanate to generate monosubstituted ureas in water. This method proceeds rapidly under microwave irradiation and tolerates a broad range of functional groups. Unlike previous strategies, it is compatible with other nucleophiles, acid-labile moieties, and most of the common protecting groups. The products precipitate out of solution, allowing facile isolation without column chromatography.

Toward the development of chemoprevention agents. Part II: Chemo-enzymatic synthesis and anti-inflammatory activities of a new class of 5-amino-2-substitutedphenyl-1,3-dioxacycloalkanes

Gu, Keli,Bi, Lanrong,Zhao, Ming,Wang, Chao,Ju, Jingfang,Peng, Shiqi

, p. 6273 - 6290 (2008/04/05)

A new series of optically pure 5-amino-2-substitutedphenyl-1,3-dioxacycloalkanes were designed and synthesized via a chemo-enzymatic combined method to develop new chemoprevention agents. Twenty-four of newly synthesized compounds significantly inhibited xylene-induced rat ear edema and exhibited comparable or better anti-inflammatory activities than the reference drug aspirin. Treatment of these anti-inflammatory agents did not prolong the tail bleeding time in rat. In addition, 5-amino-2-substitutedphenyl-1,3-dioxacycloalkanes exhibited good membrane permeability based on in vitro Caco-2 cell monolayer permeability assay. Furthermore, some preliminary structure-activity relationships were further analyzed among these compounds. Taken together, 5-amino-2-substitutedphenyl-1,3-dioxacycloalkanes may represent a new class of anti-inflammatory drugs with safer pharmacological profile.

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