Cas 1001853-66-2,(2S,6S)-2-(4-benzenesulfonyloxyphenyl)-6-[2-(4-benzenesulfonyloxyphenyl)ethyl]tetrahydropyran-4-one

1001853-66-2

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Basic information

Product Name: (2S,6S)-2-(4-benzenesulfonyloxyphenyl)-6-[2-(4-benzenesulfonyloxyphenyl)ethyl]tetrahydropyran-4-one
Synonyms: (2S,6S)-2-(4-benzenesulfonyloxyphenyl)-6-[2-(4-benzenesulfonyloxyphenyl)ethyl]tetrahydropyran-4-one
CAS NO:1001853-66-2
Molecular Formula:
Molecular Weight: 592.691
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: (2S,6S)-2-(4-benzenesulfonyloxyphenyl)-6-[2-(4-benzenesulfonyloxyphenyl)ethyl]tetrahydropyran-4-one(CAS DataBase Reference)
NIST Chemistry Reference: (2S,6S)-2-(4-benzenesulfonyloxyphenyl)-6-[2-(4-benzenesulfonyloxyphenyl)ethyl]tetrahydropyran-4-one(1001853-66-2)
EPA Substance Registry System: (2S,6S)-2-(4-benzenesulfonyloxyphenyl)-6-[2-(4-benzenesulfonyloxyphenyl)ethyl]tetrahydropyran-4-one(1001853-66-2)

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: 1001853-66-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1001853-66-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,1,8,5 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1001853-66:
(9*1)+(8*0)+(7*0)+(6*1)+(5*8)+(4*5)+(3*3)+(2*6)+(1*6)=102
102 % 10 = 2
So 1001853-66-2 is a valid CAS Registry Number.

1001853-66-2Upstream product

98-09-9 benzenesulfonyl chloride

1001853-66-2Downstream Products

886204-71-3 (2S,4R,6S)-2-(4-benzenesulfonyloxyphenyl)-6-[2-(4-benzenesulfonyloxyphenyl)ethyl]-4-{4-methoxy-2,6-bis-[2-(trimethylsilyl)ethoxymethoxy]phenyl}-tetrahydropyran

1001853-66-2Relevant academic research and scientific papers

Catalytic asymmetric hetero-Diels-Alder route to a key intermediate for the synthesis of calyxin L

Washio, Takuya,Nambu, Hisanori,Anada, Masahiro,Hashimoto, Shunichi

, p. 2606 - 2612 (2007)

A catalytic asymmetric formal synthesis of diarylheptanoid natural product calyxin L has been achieved by incorporating an enantio- and diastereoselective hetero-Diels-Alder (HDA) reaction, a Suzuki-Miyaura coupling, and a stereocontrolled catalytic hydro

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