Cas 104750-14-3,8-Benzyl-3-methyl-6,7-dihydro-5-thia-benzo[3,4]cyclohepta[1,2-b]naphthalene

104750-14-3

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Basic information

Product Name: 8-Benzyl-3-methyl-6,7-dihydro-5-thia-benzo[3,4]cyclohepta[1,2-b]naphthalene
Synonyms: 8-Benzyl-3-methyl-6,7-dihydro-5-thia-benzo[3,4]cyclohepta[1,2-b]naphthalene
CAS NO:104750-14-3
Molecular Formula:
Molecular Weight: 366.527
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: 8-Benzyl-3-methyl-6,7-dihydro-5-thia-benzo[3,4]cyclohepta[1,2-b]naphthalene(CAS DataBase Reference)
NIST Chemistry Reference: 8-Benzyl-3-methyl-6,7-dihydro-5-thia-benzo[3,4]cyclohepta[1,2-b]naphthalene(104750-14-3)
EPA Substance Registry System: 8-Benzyl-3-methyl-6,7-dihydro-5-thia-benzo[3,4]cyclohepta[1,2-b]naphthalene(104750-14-3)

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: 104750-14-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 104750-14-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,7,5 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 104750-14:
(8*1)+(7*0)+(6*4)+(5*7)+(4*5)+(3*0)+(2*1)+(1*4)=93
93 % 10 = 3
So 104750-14-3 is a valid CAS Registry Number.

104750-14-3Upstream product

72675-07-1 4-(bis-methylsulfanyl-methylene)-8-methyl-3,4-dihydro-2H-benzo[b]thiepin-5-one

104750-14-3Downstream Products

104750-14-3Relevant academic research and scientific papers

CYCLOAROMATIZATION OF α-OXOKETENDITHIOACETALS WITH BENZYLMAGNESIUM CHLORIDE: A NOVEL NAPHTHALENE ANNELATION REACTION

Balu, Maliakel P.,Singh, Gurdeep,Ila, Hiriyakkanavar,Junjappa, Hiriyakkanavar

, p. 117 - 120 (2007/10/02)

α-Oxoketendithioacetals derived from acyclic and cyclic ketones are shown to react with benzylmagnesium chloride to give novel naphthoannelated aromatic compounds by sequential 1,4- and 1,2-additions followed by subsequent cycloaromatization of the resulting carbinols.

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