Cas 478079-71-9,N-(3-FLUORO-4-MORPHOLINOPHENYL)-2-THIOPHENECARBOXAMIDE

478079-71-9

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Basic information

Product Name: N-(3-FLUORO-4-MORPHOLINOPHENYL)-2-THIOPHENECARBOXAMIDE
Synonyms: N-(3-FLUORO-4-MORPHOLINOPHENYL)-2-THIOPHENECARBOXAMIDE;N-[3-fluoro-4-(morpholin-4-yl)phenyl]thiophene-2-carboxamide
CAS NO:478079-71-9
Molecular Formula: C15H15FN2O2S
Molecular Weight: 306.36
EINECS: N/A
Product Categories: N/A
Mol File: 478079-71-9.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: N-(3-FLUORO-4-MORPHOLINOPHENYL)-2-THIOPHENECARBOXAMIDE(CAS DataBase Reference)
NIST Chemistry Reference: N-(3-FLUORO-4-MORPHOLINOPHENYL)-2-THIOPHENECARBOXAMIDE(478079-71-9)
EPA Substance Registry System: N-(3-FLUORO-4-MORPHOLINOPHENYL)-2-THIOPHENECARBOXAMIDE(478079-71-9)

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: 478079-71-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 478079-71-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,8,0,7 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 478079-71:
(8*4)+(7*7)+(6*8)+(5*0)+(4*7)+(3*9)+(2*7)+(1*1)=199
199 % 10 = 9
So 478079-71-9 is a valid CAS Registry Number.

478079-71-9Upstream product

2689-39-6 3-fluoro-4-(4-morpholinyl)nitrobenzene

478079-71-9Downstream Products

478079-71-9Relevant academic research and scientific papers

Synthesis, anti-inflammatory activity and in silico studies of some novel morpholine based carboxamides

Honavar, Premanand M.,Kumar, Vasantha,Nikhil,Kumar, Naveen,Sreenivasa,Vishwanatha,Poojary, Boja,Holla, B. Shivarama

, p. 901 - 906 (2020)

Two series of carboxamides were synthesized from 3-fluoro-4-morpholinoaniline and different substituted aromatic/heterocyclic carboxylic acids. All the compounds were characterized by IR, 1H NMR, 13C NMR and mass spectral data. The n

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