Cas 1298093-53-4,2-methyl-7-[(tetrahydro-2H-pyran-2-yl)oxy]-2,3,4,6-tetrahydro-2,6-methanobenzo[b][1,5]dioxocin-4-ol

1298093-53-4

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Basic information

Product Name: 2-methyl-7-[(tetrahydro-2H-pyran-2-yl)oxy]-2,3,4,6-tetrahydro-2,6-methanobenzo[b][1,5]dioxocin-4-ol
Synonyms: 2-methyl-7-[(tetrahydro-2H-pyran-2-yl)oxy]-2,3,4,6-tetrahydro-2,6-methanobenzo[b][1,5]dioxocin-4-ol
CAS NO:1298093-53-4
Molecular Formula:
Molecular Weight: 306.359
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: 2-methyl-7-[(tetrahydro-2H-pyran-2-yl)oxy]-2,3,4,6-tetrahydro-2,6-methanobenzo[b][1,5]dioxocin-4-ol(CAS DataBase Reference)
NIST Chemistry Reference: 2-methyl-7-[(tetrahydro-2H-pyran-2-yl)oxy]-2,3,4,6-tetrahydro-2,6-methanobenzo[b][1,5]dioxocin-4-ol(1298093-53-4)
EPA Substance Registry System: 2-methyl-7-[(tetrahydro-2H-pyran-2-yl)oxy]-2,3,4,6-tetrahydro-2,6-methanobenzo[b][1,5]dioxocin-4-ol(1298093-53-4)

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: 1298093-53-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1298093-53-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,8,0,9 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1298093-53:
(9*1)+(8*2)+(7*9)+(6*8)+(5*0)+(4*9)+(3*3)+(2*5)+(1*3)=194
194 % 10 = 4
So 1298093-53-4 is a valid CAS Registry Number.

1298093-53-4Upstream product

154714-19-9 5-hydroxy-2,2-dimethyl-4H-benzo[d][1,3]dioxin-4-one

1298093-53-4Downstream Products

1298093-53-4Relevant academic research and scientific papers

Towards a library of chromene cannabinoids: A combinatorial approach on solid supports

Kapeller, Dagmar C.,Br?se, Stefan

, p. 161 - 164 (2011/03/19)

A novel solid-phase synthesis towards classical cannabinoids is presented. Starting from immobilized salicylaldehydes the desired THC-analogous tricycles are obtained in four atom-economic steps including cleavage. The reagents of the employed reactions (domino oxa-Michael-aldol, Wittig, and Diels-Alder) can be varied easily, providing the basis for a combinatorial approach. Overall yields range from 20-60%. Georg Thieme Verlag Stuttgart New York.

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