Cas 1359984-46-5,5-[4-(trifluoromethyl)phenyl]-2,3-dihydrothieno[3,2-c] pyridin-4(5H)-one

1359984-46-5

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Basic information

Product Name: 5-[4-(trifluoromethyl)phenyl]-2,3-dihydrothieno[3,2-c] pyridin-4(5H)-one
Synonyms: 5-[4-(trifluoromethyl)phenyl]-2,3-dihydrothieno[3,2-c] pyridin-4(5H)-one
CAS NO:1359984-46-5
Molecular Formula:
Molecular Weight: 297.301
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: 5-[4-(trifluoromethyl)phenyl]-2,3-dihydrothieno[3,2-c] pyridin-4(5H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 5-[4-(trifluoromethyl)phenyl]-2,3-dihydrothieno[3,2-c] pyridin-4(5H)-one(1359984-46-5)
EPA Substance Registry System: 5-[4-(trifluoromethyl)phenyl]-2,3-dihydrothieno[3,2-c] pyridin-4(5H)-one(1359984-46-5)

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: 1359984-46-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1359984-46-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,9,9,8 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1359984-46:
(9*1)+(8*3)+(7*5)+(6*9)+(5*9)+(4*8)+(3*4)+(2*4)+(1*6)=225
225 % 10 = 5
So 1359984-46-5 is a valid CAS Registry Number.

1359984-46-5Upstream product

1352009-60-9 1-[3-(dimethylamino)acryloyl]-N-(4-(trifluoromethyl)phenyl)cyclopropanecarboxamide

1359984-46-5Downstream Products

1359984-46-5Relevant academic research and scientific papers

Lawesson's reagent-initiated domino reaction of aminopropenoyl cyclopropanes: Synthesis of thieno[3,2-c]pyridinones

Huang, Peng,Zhang, Rui,Liang, Yongjiu,Dong, Dewen

, p. 1639 - 1644 (2012)

A convenient and efficient synthesis of substituted 2,3-dihydrothieno[3,2- c]pyridin-4(5H)-ones has been developed and relies upon a domino reaction of dimethylaminopropenoyl cyclopropanes initiated by Lawesson's reagent. A mechanism involving regioselect

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