Cas 1202397-23-6,(S)-1-(1-(isopropylsulfonyl)allyl)-4-methoxybenzene

1202397-23-6

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Basic information

Product Name: (S)-1-(1-(isopropylsulfonyl)allyl)-4-methoxybenzene
Synonyms: (S)-1-(1-(isopropylsulfonyl)allyl)-4-methoxybenzene
CAS NO:1202397-23-6
Molecular Formula:
Molecular Weight: 254.35
EINECS: N/A
Product Categories: N/A
Mol File: 1202397-23-6.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: (S)-1-(1-(isopropylsulfonyl)allyl)-4-methoxybenzene(CAS DataBase Reference)
NIST Chemistry Reference: (S)-1-(1-(isopropylsulfonyl)allyl)-4-methoxybenzene(1202397-23-6)
EPA Substance Registry System: (S)-1-(1-(isopropylsulfonyl)allyl)-4-methoxybenzene(1202397-23-6)

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: 1202397-23-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1202397-23-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,2,3,9 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1202397-23:
(9*1)+(8*2)+(7*0)+(6*2)+(5*3)+(4*9)+(3*7)+(2*2)+(1*3)=116
116 % 10 = 6
So 1202397-23-6 is a valid CAS Registry Number.

1202397-23-6Upstream product

488151-80-0 3-(p-methoxyphenyl)-2-propen-1-yl methyl carbonate

1202397-23-6Downstream Products

1202397-23-6Relevant articles and documents

Iridium-catalyzed, regio- and enantioselective allylic substitution with aromatic and aliphatic sulfinates

Ueda, Mitsuhiro,Hartwig, John F.

supporting information; experimental part, p. 92 - 94 (2010/03/04)

"Chemical Equation Presented" The iridium-catalyzed allylation of sodium sulfinate to form branched allylic sulfones is reported. The reactions between various sodium sulfinates and achiral allylic carbonates occur in good yields, with high selectivity fo

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