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Morpholine-3-carboxylic acid amide is an organic compound derived from 3-Morpholinecarbonitrile (M723800). It is characterized by the presence of a morpholine ring and a carboxylic acid amide functional group, which contributes to its unique chemical properties and potential applications in various fields.

848488-74-4

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848488-74-4 Usage

Uses

Used in Pharmaceutical Industry:
Morpholine-3-carboxylic acid amide is used as a reactant in the synthesis of N-methyl pyrimidone derivatives. These derivatives have been identified as potent and orally bioavailable HIV integrase inhibitors, playing a crucial role in the development of antiretroviral drugs for the treatment of HIV/AIDS.

Check Digit Verification of cas no

The CAS Registry Mumber 848488-74-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,4,8 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 848488-74:
(8*8)+(7*4)+(6*8)+(5*4)+(4*8)+(3*8)+(2*7)+(1*4)=234
234 % 10 = 4
So 848488-74-4 is a valid CAS Registry Number.

848488-74-4SDS

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 morpholine-3-carboxamide

1.2 Other means of identification

Product number -
Other names 3-morpholinecarboxamide

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:848488-74-4 SDS

848488-74-4Relevant academic research and scientific papers

DIHYDROPYRIMIDINE COMPOUNDS AND THEIR APPLICATION IN PHARMACEUTICALS

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Paragraph 0512 - 0551, (2015/06/10)

Provided herein are dihydropyrimidine compounds and their pharmaceutical applications, especially for use in treating and preventing HBV diseases. Specifically, provided herein are compounds having Formula (I) or (Ia), or an enantiomer, a diastereoisomer, a tautomer, a hydrate, a solvate, or a pharmaceutically acceptable salt thereof, wherein the variables of the formulas are as defined in the specification. Also provided herein is the use of the compounds having Formula (I) or (Ia), or an enantiomer, a diastereoisomer, a tautomer, a hydrate, a solvate, or a pharmaceutically acceptable salt thereof for treating and preventing HBV diseases.

DIHYDROPYRIMIDINE COMPOUNDS AND THEIR APPLICATION IN PHARMACEUTICALS

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Paragraph 00232, (2014/03/25)

Provided herein are dihydropyrimidine compounds and their pharmaceutical applications, especially for use in treating and preventing HBV diseases. Specifically,provided herein are compounds having Formula (I) or (Ia), or an enantiomer, a diastereoisomer, a tautomer, a hydrate, a solvate, or a pharmaceutically acceptable salt thereof, wherein the variables of the formulas are as defined in the specification. Also provided herein is the use of the compounds having Formula (I) or (Ia), or an enantiomer, a diastereoisomer, a tautomer, a hydrate, a solvate, or a pharmaceutically acceptable salt thereof for treating and preventing HBV diseases.

BETA CARBOLINES AND USES THEREOF

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Page/Page column 46-47, (2009/06/27)

This invention provides beta-carboline compounds of formula I: wherein R1, R2, R3, R4, R5, G, and x are as described in the specification. The compounds are useful for treating cancer and inflammatory disorders.

QUINAZOLINE DERIVATIVES

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Page/Page column 106, (2008/06/13)

The invention concerns quinazoline derivatives of Formula (I) wherein each of R1, R3, R20, X1, X2, Z, W, (a) and (q) have any of the meanings defined in the description; processes for their preparation, pharmaceutical compositions containing them and their use in the manufacture of a medicament for use as an antiproliferative agent in the prevention or treatment of turnours which are sensitive to inhibition of erbB receptor tyrosine kinases, particularly EGFR tyrosine kinase.

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