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2(1H)-Azecinone, 3,4,7,8,9,10-hexahydro-1-(phenylmethyl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138403-72-2

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138403-72-2 Usage

Classification

Hexahydroazecinone

Structure

Six-membered nitrogen-containing ring

Chirality

Chiral molecule, exists in (E) and (Z) isomers

Usage

Building block in the synthesis of pharmaceuticals and natural products

Reactivity

Versatile reactivity

Biological activity

Potential biological activity

(E)-isomer interest

Potential antineoplastic agent

(E)-isomer studies

Cytotoxicity and antitumor properties

Check Digit Verification of cas no

The CAS Registry Mumber 138403-72-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,4,0 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 138403-72:
(8*1)+(7*3)+(6*8)+(5*4)+(4*0)+(3*3)+(2*7)+(1*2)=122
122 % 10 = 2
So 138403-72-2 is a valid CAS Registry Number.

138403-72-2SDS

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 1-benzyl-2,3,4,5,8,9-hexahydroazecin-10-one

1.2 Other means of identification

Product number -
Other names 2(1H)-Azecinone,3,4,7,8,9,10-hexahydro-1-(phenylmethyl)-,(E)

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:138403-72-2 SDS

138403-72-2Upstream product

138403-72-2Relevant academic research and scientific papers

An Unexpected Reversal in the Stereochemistry of Transannular Cyclizations. A Stereoselective Synthesis of (+/-)-Epilupinine

Edstrom, Eric D.

, p. 5709 - 5712 (1991)

The transannular cyclizations of N-benzylhexahydroazec-5-en-2-one and N-benzylhexahydroazon-5-en-2-one using iodine or phenylselenyl bromide affords substituted quinolizidines and indolizidines, respectively.In the case of the ten-membered ring lactams an

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