Basic information

Product Name: Cyclohexanone, 2-(4-morpholinylphenylmethyl)-
Synonyms:
CAS NO:26598-89-0
Molecular Formula: C17H23NO2
Molecular Weight: 273.375
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Cyclohexanone, 2-(4-morpholinylphenylmethyl)-(CAS DataBase Reference)
NIST Chemistry Reference: Cyclohexanone, 2-(4-morpholinylphenylmethyl)-(26598-89-0)
EPA Substance Registry System: Cyclohexanone, 2-(4-morpholinylphenylmethyl)-(26598-89-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 26598-89-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 26598-89-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,5,9 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 26598-89:
(7*2)+(6*6)+(5*5)+(4*9)+(3*8)+(2*8)+(1*9)=160
160 % 10 = 0
So 26598-89-0 is a valid CAS Registry Number.

26598-89-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	2-[(4-morpholin-2-ylphenyl)methyl]cyclohexan-1-one

1.2 Other means of identification

Product number	-
Other names	Cyclohexanone,2-(4-morpholinylphenylmethyl)

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:26598-89-0 SDS

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26598-89-0Relevant academic research and scientific papers

Diastereoselektive Synthese neuartiger Mannich-Basen mittels Titanderivaten

Seebach, Dieter,Betschart, Claudia,Schiess, Martin

, p. 1593 - 1597 (1984)

Trichlorotitanium dialkylamino-alkoxides (2; titanates of N,O-hemiacetals) are generated either from the corresponding lithium alkoxides and titanium tetrachloride (Scheme I) or by addition of trichloro-dialkylamino-titanium to aldehydes.The electrophilic

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