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165683-59-0

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165683-59-0 Usage

Classification

Cyclic ketone

Structure

Contains an oxaspiro ring structure

Potential pharmacological and biological activities

Studied for its potential as a psychoactive substance

Regulations and controls

Subject to regulations and controls in many countries

Need for further research

More research is needed to fully understand its properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 165683-59-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,6,8 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 165683-59:
(8*1)+(7*6)+(6*5)+(5*6)+(4*8)+(3*3)+(2*5)+(1*9)=170
170 % 10 = 0
So 165683-59-0 is a valid CAS Registry Number.

165683-59-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-oxa-3-azaspiro[5.5]undecane-2,11-dione

1.2 Other means of identification

Product number -
Other names 1-Oxa-3-azaspiro[5.5]undecane-2,7-dione(9CI)

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:165683-59-0 SDS

165683-59-0Downstream Products

165683-59-0Relevant articles and documents

Tandem Zinc Mediated Reductive Cleavage-Reductive Amination as a New Approach to Substituted Pyrrolidines from Homoallylic Amines

Vanucci, Corinne,Brusson, Xavier,Verdel, Valerie,Zana, Frederique,Dhomane, Hamid,Lhommet, Gerard

, p. 2971 - 2974 (2007/10/02)

N-Boc or N-Cbz homoallylic amines are converted in four steps into pyrrolidines through a sequence involving as a key-step a tandem zinc mediated reductive amination from an intermediate 1,3-oxazin-2-one

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