Cas 1188296-99-2,N-[1-ethyl-3-(4-methoxyphenoxy)prop-2-yn-1-yl]-N-(furan-2-ylmethyl)-4-methylbenzenesulfonamide

1188296-99-2

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Basic information

Product Name: N-[1-ethyl-3-(4-methoxyphenoxy)prop-2-yn-1-yl]-N-(furan-2-ylmethyl)-4-methylbenzenesulfonamide
Synonyms: N-[1-ethyl-3-(4-methoxyphenoxy)prop-2-yn-1-yl]-N-(furan-2-ylmethyl)-4-methylbenzenesulfonamide
CAS NO:1188296-99-2
Molecular Formula:
Molecular Weight: 439.532
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: N-[1-ethyl-3-(4-methoxyphenoxy)prop-2-yn-1-yl]-N-(furan-2-ylmethyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[1-ethyl-3-(4-methoxyphenoxy)prop-2-yn-1-yl]-N-(furan-2-ylmethyl)-4-methylbenzenesulfonamide(1188296-99-2)
EPA Substance Registry System: N-[1-ethyl-3-(4-methoxyphenoxy)prop-2-yn-1-yl]-N-(furan-2-ylmethyl)-4-methylbenzenesulfonamide(1188296-99-2)

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: 1188296-99-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1188296-99-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,8,2,9 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1188296-99:
(9*1)+(8*1)+(7*8)+(6*8)+(5*2)+(4*9)+(3*6)+(2*9)+(1*9)=212
212 % 10 = 2
So 1188296-99-2 is a valid CAS Registry Number.

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1188296-99-2Relevant academic research and scientific papers

Gold catalysis: Switching the pathway of the furan-yne cyclization

Hashmi, A. Stephen K.,Rudolph, Matthias,Huck, Juergen,Frey, Wolfgang,Bats, Jan W.,Hamzic, Melissa

supporting information; experimental part, p. 5848 - 5852 (2009/12/06)

Changing tracks: By the use of alkynyl ethers as directing elements, the furan-yne cyclization enters a new reaction pathway. Instead of phenols, tetracycles containing two heteroatoms and two new stereocenters are formed (see scheme).

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