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2-(morpholin-4-ylmethyl)cyclohexanone hydrochloride (1:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37408-97-2

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37408-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37408-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,4,0 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 37408-97:
(7*3)+(6*7)+(5*4)+(4*0)+(3*8)+(2*9)+(1*7)=132
132 % 10 = 2
So 37408-97-2 is a valid CAS Registry Number.

37408-97-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(morpholin-4-ylmethyl)cyclohexan-1-one,hydrochloride

1.2 Other means of identification

Product number -
Other names 1-(4-Morpholinylmethyl)-2-cyclohexanone hydrochloride

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:37408-97-2 SDS

37408-97-2Downstream Products

37408-97-2Relevant academic research and scientific papers

Synthesis and cytotoxic evaluation of some Mannich bases of alicyclic ketones

Dimmock,Chamankhah,Seniuk,Allen,Kao,Halleran

, p. 668 - 671 (2007/10/03)

A number of Mannich bases of alicyclic ketones containing one and two basic centres were prepared in order to evaluate the theory of sequential cytotoxicity and develop structure-activity relationships in these series of compounds. The compounds were evaluated in vitro against murine P388 D1 lymphocytic leukemia cells. The data generated supported the theory of sequential cytotoxicity and in general, compounds containing alicyclic rings of five and six carbon atoms possessed greater activity than the corresponding dodecyl analogues. Those Mannich bases containing dialkylamino groups were associated with greater cytotoxicity than related compounds possessing a basic heterocycle. Calculations of the atomic charges of the enone groups from selected compounds afforded some rationalization for the cytotoxic screening results.

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