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79378-15-7

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79378-15-7 Usage

Appearance

Yellow solid The compound is a yellow-colored solid in its pure form.

Solubility

Soluble in organic solvents It can dissolve in organic solvents, such as ethanol, acetone, and dichloromethane.

Morpholine ring

Present The compound contains a morpholine ring, which is a five-membered heterocyclic ring with one oxygen and four carbon atoms.

Nitrophenyl group

Present The compound also contains a nitrophenyl group, which is a phenyl ring substituted with a nitro group (-NO2).

Use in synthesis

Building block for pharmaceuticals and fine chemicals Due to its unique structure, the compound is a useful building block for the synthesis of various pharmaceuticals and fine chemicals.

Application

Organic synthesis reagent It is commonly used as a reagent in organic synthesis for the preparation of biologically active compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 79378-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,7 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79378-15:
(7*7)+(6*9)+(5*3)+(4*7)+(3*8)+(2*1)+(1*5)=177
177 % 10 = 7
So 79378-15-7 is a valid CAS Registry Number.

79378-15-7SDS

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-morpholino-1-(4-nitrophenyl)ethan-1-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:79378-15-7 SDS

79378-15-7Relevant articles and documents

THIA-TETRAAZAACENAPHTHYLENE KINASE INHIBITORS

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Page/Page column 115, (2008/06/13)

The present invention is directed to novel thia-tetraazaacenaphthylene compounds of Formula (I): and pharmaceutically acceptable forms thereof and their synthesis and use as inhibitors of ATP-protein kinase interactions.

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