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(21aR)-10-(3-aminopropyl)octadecahydro-2H-pyrido[1,2-f][1,6]diazacyclooctadecin-11(6H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53602-28-1

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53602-28-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53602-28-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,0 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 53602-28:
(7*5)+(6*3)+(5*6)+(4*0)+(3*2)+(2*2)+(1*8)=101
101 % 10 = 1
So 53602-28-1 is a valid CAS Registry Number.

53602-28-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (18R)-6-(3-aminopropyl)-1,6-diazabicyclo[16.4.0]docosan-7-one

1.2 Other means of identification

Product number -
Other names Neooncinotine

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:53602-28-1 SDS

53602-28-1Downstream Products

53602-28-1Relevant academic research and scientific papers

Efficient syntheses of oncinotine and neooncinotine

Hou, Duen-Ren,Cheng, Hsiu-Yi,Wang, Eng-Chi

, p. 6094 - 6099 (2007/10/03)

We have synthesized two natural alkaloids, oncinotine (1) and neooncinotine (2), by means of efficient ring-closing metathesis (RCM) reactions. The required dienes for RCM were assembled from three basic components: 2-allylpiperidine (5), 9-decenoic acid (6), and diamines 7. We developed two different methods to achieve the linkage: the Michael addition of acrylamide and two amidations of succinic anhydride. The Grubbs catalyst was used to form the 17- and 18-membered lactams in 50% and 68% yields, respectively.

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