Cas 89353-91-3,(1beta,2alpha,11alpha,12alpha)-1,2,11,12-tetrahydroxy-11,20-epoxypicrasa-3,13(21)-dien-16-one

89353-91-3

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Basic information

Product Name: (1beta,2alpha,11alpha,12alpha)-1,2,11,12-tetrahydroxy-11,20-epoxypicrasa-3,13(21)-dien-16-one
Synonyms: Shinjulactone A
CAS NO:89353-91-3
Molecular Formula: C₂₀H₂₆O₇
Molecular Weight: 378.4162
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: 611.1°C at 760 mmHg
Flash Point: 219.1°C
Appearance: N/A
Density: 1.47g/cm³
Vapor Pressure: 1.73E-17mmHg at 25°C
Refractive Index: 1.649
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (1beta,2alpha,11alpha,12alpha)-1,2,11,12-tetrahydroxy-11,20-epoxypicrasa-3,13(21)-dien-16-one(CAS DataBase Reference)
NIST Chemistry Reference: (1beta,2alpha,11alpha,12alpha)-1,2,11,12-tetrahydroxy-11,20-epoxypicrasa-3,13(21)-dien-16-one(89353-91-3)
EPA Substance Registry System: (1beta,2alpha,11alpha,12alpha)-1,2,11,12-tetrahydroxy-11,20-epoxypicrasa-3,13(21)-dien-16-one(89353-91-3)

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: 89353-91-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 89353-91-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,3,5 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89353-91:
(7*8)+(6*9)+(5*3)+(4*5)+(3*3)+(2*9)+(1*1)=173
173 % 10 = 3
So 89353-91-3 is a valid CAS Registry Number.

89353-91-3Upstream product

89353-91-3Downstream Products

981-15-7 ailanthone

89353-91-3Relevant academic research and scientific papers

Constituents of Seeds of Ailanthus altissima SWINGLE. Isolation and Structures of Shinjuglycosides A, B, C, and D

Yoshimura, Shin,Ishibashi, Masami,Tsuyuki, Takahiko,Takahashi, Takeyoshi,Matsushita, Kazuhiro

, p. 2496 - 2501 (1984)

Four bitter quassinoid glycosides, shinjuglycosides A, B, C, and D were isolated from seeds of Ailanthus altissima SWINGLE and their structures were established to be 2-β-D-glycopyranosides of chaparrin, shinjulactone A, amarolide 11-acetate, and amarolide, respectively, from spectral data and enzymatic or acid-catalyzed hydrolysis.

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