Cas 116450-93-2,1H-Indene-1,3(2H)-dione, 2-[dihydro-5-[(phenylmethoxy)methyl]-2(3H)-furanylidene]-, (R)-

116450-93-2

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Basic information

Product Name: 1H-Indene-1,3(2H)-dione, 2-[dihydro-5-[(phenylmethoxy)methyl]-2(3H)-furanylidene]-, (R)-
Synonyms:
CAS NO:116450-93-2
Molecular Formula: C21H18O4
Molecular Weight: 334.372
EINECS: N/A
Product Categories: N/A
Mol File: 116450-93-2.mol

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: 1H-Indene-1,3(2H)-dione, 2-[dihydro-5-[(phenylmethoxy)methyl]-2(3H)-furanylidene]-, (R)-(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Indene-1,3(2H)-dione, 2-[dihydro-5-[(phenylmethoxy)methyl]-2(3H)-furanylidene]-, (R)-(116450-93-2)
EPA Substance Registry System: 1H-Indene-1,3(2H)-dione, 2-[dihydro-5-[(phenylmethoxy)methyl]-2(3H)-furanylidene]-, (R)-(116450-93-2)

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: 116450-93-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 116450-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,4,5 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 116450-93:
(8*1)+(7*1)+(6*6)+(5*4)+(4*5)+(3*0)+(2*9)+(1*3)=112
112 % 10 = 2
So 116450-93-2 is a valid CAS Registry Number.

116450-93-2Upstream product

116450-93-2Downstream Products

116450-93-2Relevant academic research and scientific papers

Condensation of a Chiral Tetrahydro-2-furanthione with Diazocarbonyl Compounds

Takano, Seiichi,Tomita, Schun'ichi,Takahashi, Michiyasu,Ogasawara, Kunio

, p. 1116 - 1117 (2007/10/02)

Reaction of (R)-5-(benzyloxymethyl)tetrahydro-2-furanthione (2), prepared from the corresponding furanone 1, with the diazocarbonyl compounds 3a-c in the presence of rhodium(II) acetate afforded the 2-(acylmethylene)tetrahydrofuran derivatives 4a-c in goo

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