Cas 199588-37-9,3-Hexanoyl-3-phenylselanyl-4-[(1R,2R)-1,2,3-tris-(tert-butyl-dimethyl-silanyloxy)-propyl]-dihydro-furan-2-one

199588-37-9

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Basic information

Product Name: 3-Hexanoyl-3-phenylselanyl-4-[(1R,2R)-1,2,3-tris-(tert-butyl-dimethyl-silanyloxy)-propyl]-dihydro-furan-2-one
Synonyms:
CAS NO:199588-37-9
Molecular Formula:
Molecular Weight: 772.16
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-Hexanoyl-3-phenylselanyl-4-[(1R,2R)-1,2,3-tris-(tert-butyl-dimethyl-silanyloxy)-propyl]-dihydro-furan-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 3-Hexanoyl-3-phenylselanyl-4-[(1R,2R)-1,2,3-tris-(tert-butyl-dimethyl-silanyloxy)-propyl]-dihydro-furan-2-one(199588-37-9)
EPA Substance Registry System: 3-Hexanoyl-3-phenylselanyl-4-[(1R,2R)-1,2,3-tris-(tert-butyl-dimethyl-silanyloxy)-propyl]-dihydro-furan-2-one(199588-37-9)

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: 199588-37-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 199588-37-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,5,8 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 199588-37:
(8*1)+(7*9)+(6*9)+(5*5)+(4*8)+(3*8)+(2*3)+(1*7)=219
219 % 10 = 9
So 199588-37-9 is a valid CAS Registry Number.

199588-37-9Upstream product

199588-37-9Downstream Products

199588-37-9Relevant academic research and scientific papers

Asymmetric total synthesis of syringolide 1, a nonproteinaceous elicitor

Ishihara, Jun,Sugimoto, Tetsuya,Murai, Akio

, p. 16029 - 16040 (1997)

An asymmetric synthesis of syringolide 1, one of the elicitors produced by Pseudomonas syringae pv. tomato, is described. It was synthesized from 2- (t-oxocthyl)-2-buten-4-olide via 1,4-addition of alkenyl cuprate, asymmetric dihydroxylation, and intramolecular Michael reaction.

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