Cas 668441-11-0,2-phenyl-3-[(1'S,2'R)-1'-(2',3'-O-isopropylidene-1',2',3'-trihydroxypropyl)]-5,6-dihydro-1,4-dithiin

668441-11-0

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Basic information

Product Name: 2-phenyl-3-[(1'S,2'R)-1'-(2',3'-O-isopropylidene-1',2',3'-trihydroxypropyl)]-5,6-dihydro-1,4-dithiin
Synonyms: 2-phenyl-3-[(1'S,2'R)-1'-(2',3'-O-isopropylidene-1',2',3'-trihydroxypropyl)]-5,6-dihydro-1,4-dithiin
CAS NO:668441-11-0
Molecular Formula:
Molecular Weight: 324.465
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-phenyl-3-[(1'S,2'R)-1'-(2',3'-O-isopropylidene-1',2',3'-trihydroxypropyl)]-5,6-dihydro-1,4-dithiin(CAS DataBase Reference)
NIST Chemistry Reference: 2-phenyl-3-[(1'S,2'R)-1'-(2',3'-O-isopropylidene-1',2',3'-trihydroxypropyl)]-5,6-dihydro-1,4-dithiin(668441-11-0)
EPA Substance Registry System: 2-phenyl-3-[(1'S,2'R)-1'-(2',3'-O-isopropylidene-1',2',3'-trihydroxypropyl)]-5,6-dihydro-1,4-dithiin(668441-11-0)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 668441-11-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 668441-11-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,8,4,4 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 668441-11:
(8*6)+(7*6)+(6*8)+(5*4)+(4*4)+(3*1)+(2*1)+(1*1)=180
180 % 10 = 0
So 668441-11-0 is a valid CAS Registry Number.

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668441-11-0Relevant academic research and scientific papers

Asymmetric induction in the coupling of 5,6-dihydro-1,4-dithiins with chiral aldehydes. A new synthetic approach to polyhydroxylated compounds

Caputo, Romualdo,Longobardo, Luigi,Palumbo, Giovanni,Pedatella, Silvana,Giordano, Federico

, p. 11857 - 11866 (1996)

A new strategy is designed to synthesize polyhydroxyl compounds (and/or carbohydrates) by coupling of 5,6-dihydro-1,4-dithiins - carrying a vinylic hydrogen atom - with chiral aldehydes and, in sequence, stereoselective removal of the dithiodimethylene di

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