Cas 78424-64-3,6-Phenylsulfanyl-5,6-dihydro-4H-pyran-3-carboxylic acid ethyl ester

78424-64-3

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Basic information

Product Name: 6-Phenylsulfanyl-5,6-dihydro-4H-pyran-3-carboxylic acid ethyl ester
Synonyms: 6-Phenylsulfanyl-5,6-dihydro-4H-pyran-3-carboxylic acid ethyl ester
CAS NO:78424-64-3
Molecular Formula:
Molecular Weight: 264.345
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: 6-Phenylsulfanyl-5,6-dihydro-4H-pyran-3-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 6-Phenylsulfanyl-5,6-dihydro-4H-pyran-3-carboxylic acid ethyl ester(78424-64-3)
EPA Substance Registry System: 6-Phenylsulfanyl-5,6-dihydro-4H-pyran-3-carboxylic acid ethyl ester(78424-64-3)

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: 78424-64-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 78424-64-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,4,2 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78424-64:
(7*7)+(6*8)+(5*4)+(4*2)+(3*4)+(2*6)+(1*4)=153
153 % 10 = 3
So 78424-64-3 is a valid CAS Registry Number.

78424-64-3Upstream product

78424-63-2 ethyl 2-acetoxy-6-phenylthio-2,3,5,6-tetrahydro-4H-pyran-3-carboxylate

78424-64-3Downstream Products

78424-64-3Relevant academic research and scientific papers

SYNTHETIC STUDIES ON IRIDOID TERPENES VIA REGIOSELECTIVE SULFENYLATION OF β-KETOESTERS AND OXIDATIVE CLEAVAGE OF β-THIOALCOHOLS - A NOVEL SYNTHETIC ROUTE TO (+/-)-LOGANIN -

Hiroi, Kunio,Miura, Hideyuki,Kotsuji, Kumiko,Sato, Shuko

, p. 559 - 562 (2007/10/02)

Regioselective sulfenylation of ethyl 2-oxocyclopentanecarboxylate (3) and methyl 7,7-ethylenedioxy-3-oxobicyclooctane-2-carboxylate (12), followed by NaBH4 reduction and subsequent oxidative ring cleavage with lead(IV) acetate gave ethyl 2-acetoxy

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