Cas 1007599-19-0,5-[4-hydroxy-6-(4-hydroxyphenethyl)tetrahydro-2H-pyran-2-yl]-3-methoxybenzene-1,2-diol

1007599-19-0

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Basic information

Product Name: 5-[4-hydroxy-6-(4-hydroxyphenethyl)tetrahydro-2H-pyran-2-yl]-3-methoxybenzene-1,2-diol
Synonyms: 5-[4-hydroxy-6-(4-hydroxyphenethyl)tetrahydro-2H-pyran-2-yl]-3-methoxybenzene-1,2-diol
CAS NO:1007599-19-0
Molecular Formula:
Molecular Weight: 360.407
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: 5-[4-hydroxy-6-(4-hydroxyphenethyl)tetrahydro-2H-pyran-2-yl]-3-methoxybenzene-1,2-diol(CAS DataBase Reference)
NIST Chemistry Reference: 5-[4-hydroxy-6-(4-hydroxyphenethyl)tetrahydro-2H-pyran-2-yl]-3-methoxybenzene-1,2-diol(1007599-19-0)
EPA Substance Registry System: 5-[4-hydroxy-6-(4-hydroxyphenethyl)tetrahydro-2H-pyran-2-yl]-3-methoxybenzene-1,2-diol(1007599-19-0)

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: 1007599-19-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1007599-19-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,7,5,9 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1007599-19:
(9*1)+(8*0)+(7*0)+(6*7)+(5*5)+(4*9)+(3*9)+(2*1)+(1*9)=150
150 % 10 = 0
So 1007599-19-0 is a valid CAS Registry Number.

1007599-19-0Upstream product

1172115-60-4 C₂₈H₃₂O₁₀

1007599-19-0Downstream Products

1007599-19-0Relevant academic research and scientific papers

Synthesis of a novel diarylheptanoid isolated from Zingiber officinale

Parker, Gregory D.,Seden, Peter T.,Willis, Christine L.

scheme or table, p. 3686 - 3689 (2009/10/04)

Syntheses of 4-acetoxy-2,6-disubstituted tetrahydropyrans via Prins cyclisation of homoallylic alcohols with benzylic aldehydes are described and the methodology is applied in the total synthesis of diarylheptanoid 1 confirming both the structure and abso

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