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16041-56-8

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16041-56-8 Usage

General Description

(2R*,4AR*,8AR*)-2-METHYLOCTAHYDRO-4(1H)-QUINOLINONE is a chemical compound with a molecular formula of C10H17NO. It is a bicyclic amine that belongs to the class of quinolines, which are heterocyclic compounds containing a benzene ring fused to a pyridine ring. (2R*,4AR*,8AR*)-2-METHYLOCTAHYDRO-4(1H)-QUINOLINONE is used in organic synthesis as a building block for the preparation of other complex molecules. It is also potentially useful in medicinal chemistry due to its structural features, and it may have biological activity that could be of interest for pharmaceutical research. Additionally, (2R*,4AR*,8AR*)-2-METHYLOCTAHYDRO-4(1H)-QUINOLINONE may have other industrial applications, such as in the production of fine chemicals or specialty materials.

Check Digit Verification of cas no

The CAS Registry Mumber 16041-56-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,4 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16041-56:
(7*1)+(6*6)+(5*0)+(4*4)+(3*1)+(2*5)+(1*6)=78
78 % 10 = 8
So 16041-56-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H17NO/c1-7-6-10(12)8-4-2-3-5-9(8)11-7/h7-9,11H,2-6H2,1H3/t7-,8-,9-/m1/s1

16041-56-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,4aR,8aR)-2-Methyloctahydro-4(1H)-quinolinone

1.2 Other means of identification

Product number -
Other names 2e-methyl-4-oxo-decahydroquinoline

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:16041-56-8 SDS

16041-56-8Relevant articles and documents

STEREOCHEMISTRY OF NITROGEN HETEROCYCLES. 67. TRANSFORMATIONS OF STEREOISOMERIC 1-CHLORO-2-METHYL-4-KETO-trans-DECAHYDROQUINOLINES IN AN ACIDIC MEDIUM

Litvinenko, G. S.,Voronenko, L. A.,Isakova, L. A.

, p. 906 - 913 (2007/10/02)

It is shown that epimeric 1-chloro-2-methyl-4-keto-trans-decahydroquinolines in an acidic medium undergo intermolecular monochlorination in the α position relative to the carbonyl group with the formation of epimeric 3e-chloro- and 10a-chloro-2-methyl-4-keto-trans-decahydroquinolines and 2-methyl-4-keto-10-chloro-cis-decahydroquinolines.The mechanism of the transformations is examined, and an assumption regarding the possibility of cis-trans isomerization of the intermediately formed ?-chloronium complex is expressed.

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