Cas 320342-52-7,3-(5-allyl-2,2-dimethyl-[1,3]dioxan-5-yl)-1-(5-triisopropylsilanyloxy-furan-3-yl)-propan-1-ol

320342-52-7

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Basic information

Product Name: 3-(5-allyl-2,2-dimethyl-[1,3]dioxan-5-yl)-1-(5-triisopropylsilanyloxy-furan-3-yl)-propan-1-ol
Synonyms: 3-(5-allyl-2,2-dimethyl-[1,3]dioxan-5-yl)-1-(5-triisopropylsilanyloxy-furan-3-yl)-propan-1-ol
CAS NO:320342-52-7
Molecular Formula:
Molecular Weight: 452.707
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: 3-(5-allyl-2,2-dimethyl-[1,3]dioxan-5-yl)-1-(5-triisopropylsilanyloxy-furan-3-yl)-propan-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: 3-(5-allyl-2,2-dimethyl-[1,3]dioxan-5-yl)-1-(5-triisopropylsilanyloxy-furan-3-yl)-propan-1-ol(320342-52-7)
EPA Substance Registry System: 3-(5-allyl-2,2-dimethyl-[1,3]dioxan-5-yl)-1-(5-triisopropylsilanyloxy-furan-3-yl)-propan-1-ol(320342-52-7)

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: 320342-52-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 320342-52-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,0,3,4 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 320342-52:
(8*3)+(7*2)+(6*0)+(5*3)+(4*4)+(3*2)+(2*5)+(1*2)=87
87 % 10 = 7
So 320342-52-7 is a valid CAS Registry Number.

320342-52-7Upstream product

80522-42-5 triisopropylsilyl trifluoromethanesulfonate

320342-52-7Downstream Products

320342-52-7Relevant academic research and scientific papers

Synthetic studies on azadirachtin: Asymmetric synthesis of the tetracyclic decalin part of azadirachtin

Kanoh,Ishihara,Yamamoto,Murai

, p. 1878 - 1893 (2000)

A synthesis of the tetracyclic decalin part of azadirachtin in the naturally occurring form is described. The key reactions involve the Corey-Bakshi-Shibata (CBS) asymmetric reduction of the ketone, and an intramolecular Diels-Alder (IMDA) reaction.

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