Cas 107515-71-9,Butyl-[3-ethyl-5-methyl-5-phenylselanylmethyl-dihydro-furan-(2E)-ylidene]-amine

107515-71-9

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Basic information

Product Name: Butyl-[3-ethyl-5-methyl-5-phenylselanylmethyl-dihydro-furan-(2E)-ylidene]-amine
Synonyms:
CAS NO:107515-71-9
Molecular Formula:
Molecular Weight: 352.378
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: Butyl-[3-ethyl-5-methyl-5-phenylselanylmethyl-dihydro-furan-(2E)-ylidene]-amine(CAS DataBase Reference)
NIST Chemistry Reference: Butyl-[3-ethyl-5-methyl-5-phenylselanylmethyl-dihydro-furan-(2E)-ylidene]-amine(107515-71-9)
EPA Substance Registry System: Butyl-[3-ethyl-5-methyl-5-phenylselanylmethyl-dihydro-furan-(2E)-ylidene]-amine(107515-71-9)

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: 107515-71-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 107515-71-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,5,1 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 107515-71:
(8*1)+(7*0)+(6*7)+(5*5)+(4*1)+(3*5)+(2*7)+(1*1)=109
109 % 10 = 9
So 107515-71-9 is a valid CAS Registry Number.

107515-71-9Upstream product

10264-16-1 N-butyl-butyramide

107515-71-9Downstream Products

107515-92-4 4-Butylaminomethyl-2-methyl-1-phenylselanyl-hexan-2-ol

107515-71-9Relevant academic research and scientific papers

Organoselenium-Induced Cyclization of Olefinic Imidates and Amides. Selective Synthesis of Lactams or Iminolactones

Toshimitsu, Akio,Terao, Keiji,Uemura, Sakae

, p. 2018 - 2026 (2007/10/02)

Lactams were formed selectively by the cyclization of olefinic imidates through the addition of a phenylseleno group to the double bond.Similar cyclization of olefinic amides, on the other hand, afforded either iminolactones or lactams depending on the st

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