Cas 888949-16-4,(5S)-2-methyl-5-[(1S)-1-tert-butoxycarbonylamino-2-tert-butyldiphenylsilanyloxyethyl]-3-oxo-2,3,4,5-tetrahydropyridazine

888949-16-4

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Basic information

Product Name: (5S)-2-methyl-5-[(1S)-1-tert-butoxycarbonylamino-2-tert-butyldiphenylsilanyloxyethyl]-3-oxo-2,3,4,5-tetrahydropyridazine
Synonyms: (5S)-2-methyl-5-[(1S)-1-tert-butoxycarbonylamino-2-tert-butyldiphenylsilanyloxyethyl]-3-oxo-2,3,4,5-tetrahydropyridazine
CAS NO:888949-16-4
Molecular Formula:
Molecular Weight: 509.721
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: (5S)-2-methyl-5-[(1S)-1-tert-butoxycarbonylamino-2-tert-butyldiphenylsilanyloxyethyl]-3-oxo-2,3,4,5-tetrahydropyridazine(CAS DataBase Reference)
NIST Chemistry Reference: (5S)-2-methyl-5-[(1S)-1-tert-butoxycarbonylamino-2-tert-butyldiphenylsilanyloxyethyl]-3-oxo-2,3,4,5-tetrahydropyridazine(888949-16-4)
EPA Substance Registry System: (5S)-2-methyl-5-[(1S)-1-tert-butoxycarbonylamino-2-tert-butyldiphenylsilanyloxyethyl]-3-oxo-2,3,4,5-tetrahydropyridazine(888949-16-4)

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: 888949-16-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 888949-16-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,8,9,4 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 888949-16:
(8*8)+(7*8)+(6*8)+(5*9)+(4*4)+(3*9)+(2*1)+(1*6)=264
264 % 10 = 4
So 888949-16-4 is a valid CAS Registry Number.

888949-16-4Upstream product

888949-16-4Downstream Products

888949-16-4Relevant academic research and scientific papers

Investigation of a route to ibotenic acid analogues via a reduced pyroglutamate template

Ahmed, Omar,Hitchcock, Peter B.,Young, Douglas W.

, p. 1596 - 1603 (2006)

Two alternative "ring switch" based syntheses have been shown to give access to the reduced protected homochiral analogues, 27, 28 and 36, of the CNS active compound ibotenic acid. The Royal Society of Chemistry 2006.

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