Cas 1068012-35-0,(2R,2'R,6'R)-2-(1,3-dioxo[1,3]dithian-2-yl)tetrahydropyran

1068012-35-0

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Basic information

Product Name: (2R,2'R,6'R)-2-(1,3-dioxo[1,3]dithian-2-yl)tetrahydropyran
Synonyms: (2R,2'R,6'R)-2-(1,3-dioxo[1,3]dithian-2-yl)tetrahydropyran
CAS NO:1068012-35-0
Molecular Formula:
Molecular Weight: 369.506
EINECS: N/A
Product Categories: N/A
Mol File: 1068012-35-0.mol
Article Data: 1

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: (2R,2'R,6'R)-2-(1,3-dioxo[1,3]dithian-2-yl)tetrahydropyran(CAS DataBase Reference)
NIST Chemistry Reference: (2R,2'R,6'R)-2-(1,3-dioxo[1,3]dithian-2-yl)tetrahydropyran(1068012-35-0)
EPA Substance Registry System: (2R,2'R,6'R)-2-(1,3-dioxo[1,3]dithian-2-yl)tetrahydropyran(1068012-35-0)

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: 1068012-35-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1068012-35-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,8,0,1 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1068012-35:
(9*1)+(8*0)+(7*6)+(6*8)+(5*0)+(4*1)+(3*2)+(2*3)+(1*5)=120
120 % 10 = 0
So 1068012-35-0 is a valid CAS Registry Number.

1068012-35-0Upstream product

501-53-1 benzyl chloroformate

1068012-35-0Downstream Products

1067639-92-2 benzyl (R)-2-([1,3]dithian-2-yl)piperidine-1-carboxylate

1068012-35-0Relevant articles and documents

Intramolecular Michael-type additions to vinyl bissulfoxides: Enantioselective synthesis of chiral aldehydes

Gehring, Timo,Podlech, Joachim,Rothenberger, Alexander

, p. 2476 - 2487 (2008)

The diastereoselective auxiliary-based intramolecular Michael-type additions to alkylidene bissulfoxides derived from dithiane and dithiolane were investigated. Utilization of substrates bearing N- and O-nucleophilic functions led to the formation of the

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