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92628-12-1

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92628-12-1 Usage

Type of compound

Cyclic ketone

Ring structure

Seven-membered ring

Presence of nitrogen atom

Yes

Spiro junction

Yes

Class

Spiro compounds

Known for

Diverse chemical and biological properties

Potential applications

Medicinal chemistry and drug discovery

Unique structural features

May contribute to potential biological activities and pharmacological properties

Further research needed

To explore potential biological activities and pharmacological properties

Check Digit Verification of cas no

The CAS Registry Mumber 92628-12-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,6,2 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 92628-12:
(7*9)+(6*2)+(5*6)+(4*2)+(3*8)+(2*1)+(1*2)=141
141 % 10 = 1
So 92628-12-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H18N2O3/c1-16-9(14)8-13-7-3-5-11(10(13)15)4-2-6-12-11/h12H,2-8H2,1H3

92628-12-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-methyl-1,9-diazaspiro[4.5]decan-10-one

1.2 Other means of identification

Product number -
Other names -

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:92628-12-1 SDS

92628-12-1Downstream Products

92628-12-1Relevant articles and documents

Spiro- and Bicyclic Azalactams by Hydrolysis of α-Chlorinated Bicyclic Amidines

Loefas, Stefan,Ahlberg, Per

, p. 583 - 586 (2007/10/02)

The synthetic potential of α-chlorinated bicyclic amidines to form spiro- and bicyclic azalactams on hydrolysis has been investigated.Thus, 2a,b, prepared by chlorination of 1a,b with carbon tetrachloride in DMF, were treated with water via hydrolysis of the amidine function and an intramolecular substitution, 2a, afforded the azaspirolactam 6a, and 2b gave the isomers 6b and 6c in the ratio 22:78, respectively.Similarly, α-chlorinated DBU 3b gave the bicyclic azalactam 10.A high-yield preparative method for obtaining the bicyclic amidine 1a was worked out on the basis of Reissert's method from 1893, starting from diethyl malonate and α-bromopropylphthalimide.

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