Cas 1330122-27-4,2-(heptafluoropropyl)-7a-phenyl-3-(2-thienylcarbonyl)octahydro-1-benzofuran-2-yl acetate

1330122-27-4

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Basic information

Product Name: 2-(heptafluoropropyl)-7a-phenyl-3-(2-thienylcarbonyl)octahydro-1-benzofuran-2-yl acetate
Synonyms: 2-(heptafluoropropyl)-7a-phenyl-3-(2-thienylcarbonyl)octahydro-1-benzofuran-2-yl acetate
CAS NO:1330122-27-4
Molecular Formula:
Molecular Weight: 538.483
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: 2-(heptafluoropropyl)-7a-phenyl-3-(2-thienylcarbonyl)octahydro-1-benzofuran-2-yl acetate(CAS DataBase Reference)
NIST Chemistry Reference: 2-(heptafluoropropyl)-7a-phenyl-3-(2-thienylcarbonyl)octahydro-1-benzofuran-2-yl acetate(1330122-27-4)
EPA Substance Registry System: 2-(heptafluoropropyl)-7a-phenyl-3-(2-thienylcarbonyl)octahydro-1-benzofuran-2-yl acetate(1330122-27-4)

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: 1330122-27-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1330122-27-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,0,1,2 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1330122-27:
(9*1)+(8*3)+(7*3)+(6*0)+(5*1)+(4*2)+(3*2)+(2*2)+(1*7)=84
84 % 10 = 4
So 1330122-27-4 is a valid CAS Registry Number.

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1330122-27-4Relevant academic research and scientific papers

Synthesis of fluoroacylated 4,5-dihydrofurans and fluoroalkylated tetrahydrofurans by the radical cyclization using manganese(III) acetate. Part II

Yilmaz, Mehmet,Pekel, A. Tarik

experimental part, p. 628 - 635 (2011/10/01)

Manganese(III) acetate-based radical cyclizations of various fluorinated 1,3-dicarbonyl compounds with alkenes produced 3-fluoroacylated 4,5-dihydrofurans and 2-acetyloxy-2-fluoroalkylated tetrahydrofurans in good yields. Mechanism was proposed for the fo

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