Cas 1002352-65-9,(4S)-4-(4-methoxybenzyl)-3-[(2E)-2-methyl-1-(phenylsulfonyl)but-2-enyl]-1,3-oxazolidin-2-one

1002352-65-9

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Basic information

Product Name: (4S)-4-(4-methoxybenzyl)-3-[(2E)-2-methyl-1-(phenylsulfonyl)but-2-enyl]-1,3-oxazolidin-2-one
Synonyms: (4S)-4-(4-methoxybenzyl)-3-[(2E)-2-methyl-1-(phenylsulfonyl)but-2-enyl]-1,3-oxazolidin-2-one
CAS NO:1002352-65-9
Molecular Formula:
Molecular Weight: 401.483
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: (4S)-4-(4-methoxybenzyl)-3-[(2E)-2-methyl-1-(phenylsulfonyl)but-2-enyl]-1,3-oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (4S)-4-(4-methoxybenzyl)-3-[(2E)-2-methyl-1-(phenylsulfonyl)but-2-enyl]-1,3-oxazolidin-2-one(1002352-65-9)
EPA Substance Registry System: (4S)-4-(4-methoxybenzyl)-3-[(2E)-2-methyl-1-(phenylsulfonyl)but-2-enyl]-1,3-oxazolidin-2-one(1002352-65-9)

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: 1002352-65-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1002352-65-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,2,3,5 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1002352-65:
(9*1)+(8*0)+(7*0)+(6*2)+(5*3)+(4*5)+(3*2)+(2*6)+(1*5)=79
79 % 10 = 9
So 1002352-65-9 is a valid CAS Registry Number.

1002352-65-9Upstream product

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1002352-65-9Relevant academic research and scientific papers

Synthesis of tyrosine-derived tetrahydroisoquinolines by Lewis acid catalyzed cyclization of N-(phenylsulfonyl)alkyloxazolidinones

Tussetschlaeger, Stefan,Baro, Angelika,Laschat, Sabine,Frey, Wolfgang

, p. 5590 - 5602 (2008/09/17)

N-Boc-protected tyrosine esters 5a,b were converted into tetrahydroisoquinolines 13 and 14 in four steps by reduction and ring closure to oxazolidinones 9 and 10, addition of benzenesulfinic acid and aldehydes to sulfones 11 and 12 and subsequent Lewis ac

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