Cas 862469-22-5,2-{5-methoxy-4-methyl-2-[(methylsulfonyl)oxy]phenyl}-propane-1,2-diol

862469-22-5

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Basic information

Product Name: 2-{5-methoxy-4-methyl-2-[(methylsulfonyl)oxy]phenyl}-propane-1,2-diol
Synonyms: 2-{5-methoxy-4-methyl-2-[(methylsulfonyl)oxy]phenyl}-propane-1,2-diol
CAS NO:862469-22-5
Molecular Formula:
Molecular Weight: 290.337
EINECS: N/A
Product Categories: N/A
Mol File: 862469-22-5.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: 2-{5-methoxy-4-methyl-2-[(methylsulfonyl)oxy]phenyl}-propane-1,2-diol(CAS DataBase Reference)
NIST Chemistry Reference: 2-{5-methoxy-4-methyl-2-[(methylsulfonyl)oxy]phenyl}-propane-1,2-diol(862469-22-5)
EPA Substance Registry System: 2-{5-methoxy-4-methyl-2-[(methylsulfonyl)oxy]phenyl}-propane-1,2-diol(862469-22-5)

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: 862469-22-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 862469-22-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,4,6 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 862469-22:
(8*8)+(7*6)+(6*2)+(5*4)+(4*6)+(3*9)+(2*2)+(1*2)=195
195 % 10 = 5
So 862469-22-5 is a valid CAS Registry Number.

862469-22-5Upstream product

862469-22-5Downstream Products

862469-22-5Relevant articles and documents

Strategies for the total asymmetric synthesis of heliannuols K and L: Scope and limitations

Lecornue, Frederic,Paugam, Renee,Ollivier, Jean

, p. 2589 - 2598 (2007/10/03)

Kulinkovich reactions of oxa-esters bearing terminal double bonds afford cyclopropanols by intramolecular cyclization. These can undergo Saegusa oxidation to provide β-chlorooxacycloalkanones and can then be then dehydrohalogenated into oxacycloalkenones.

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