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N-(2-aminophenyl)-N-[[3-[3-[4-[4-(hydroxymethyl)phenyl]-6-[(3-hydroxypyrrolidin-1-yl)methyl]-1,3-dioxan-2-yl]phenyl]phenyl]methyl]octanediamide is a complex organic compound with a molecular formula of C41H47N3O6. It is a derivative of octanedioic acid, featuring a long aliphatic chain and multiple aromatic rings. The structure includes various functional groups such as hydroxyl, amino, and pyrrolidinyl moieties, which contribute to its chemical properties and potential applications. N-(2-aminophenyl)-N-[[3-[3-[4-[4-(hydroxymethyl)phenyl]-6-[(3-hydroxypyrrolidin-1-yl)methyl]-1,3-dioxan-2-yl]phenyl]phenyl]methyl]octanediamide is characterized by its intricate arrangement of atoms and bonds, making it a challenging target for synthesis and a subject of interest in the field of organic chemistry.

5216-82-0

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5216-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5216-82-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,1 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5216-82:
(6*5)+(5*2)+(4*1)+(3*6)+(2*8)+(1*2)=80
80 % 10 = 0
So 5216-82-0 is a valid CAS Registry Number.

5216-82-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-bis((benzo[d][1,3]dioxol-5-yl)methylene)cyclohexanone

1.2 Other means of identification

Product number -
Other names 2,6-bis-(3,4-methylenedioxybenzylidene)cyclohexan-1-one

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:5216-82-0 SDS

5216-82-0Downstream Products

5216-82-0Relevant academic research and scientific papers

A novel and efficient direct aldol condensation from ketones and aromatic aldehydes catalyzed by proline-TEA through a new pathway

Wang, Jun-feng,Lei, Meng,Li, Qin,Ge, Ze-mei,Wang, Xin,Li, Run-tao

experimental part, p. 4826 - 4833 (2009/10/02)

A novel and efficient direct aldol condensation from various ketones and a wide range of aldehydes was catalyzed by l-proline-TEA (triethylamine) in MeOH at room temperature, affording the corresponding (E)-α,β-unsaturated ketones in excellent yields. By

APPROACHES TO THE TOTAL SYNTHESIS OF THE MONTANINE (AMARYLLIDACEAE) ALKALOIDS. PREPARATION OF ISOMERIC 3-ARYLOCTAHYDROINDOLES

Sanchez, Ignacio H.,Larraza, Maria Isabel,Rojas, Irma,Brena, Francisco Kuri,Flores, Humberto J.

, p. 3033 - 3039 (2007/10/02)

The preparation of various isomeric 3-arylooctahydroindoles, potential synthons for the total synthesis of the montanine-like Amaryllidaceae alkaloids, is described.

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