Cas 155814-63-4,(2S,6R,7R,9S,15S)-15-Benzyl-2,9,15-trimethyl-1,8,13,16-tetraoxa-dispiro[5.0.5.4]hexadecan-14-one

155814-63-4

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Basic information

Product Name: (2S,6R,7R,9S,15S)-15-Benzyl-2,9,15-trimethyl-1,8,13,16-tetraoxa-dispiro[5.0.5.4]hexadecan-14-one
Synonyms: (2S,6R,7R,9S,15S)-15-Benzyl-2,9,15-trimethyl-1,8,13,16-tetraoxa-dispiro[5.0.5.4]hexadecan-14-one
CAS NO:155814-63-4
Molecular Formula:
Molecular Weight: 374.477
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: (2S,6R,7R,9S,15S)-15-Benzyl-2,9,15-trimethyl-1,8,13,16-tetraoxa-dispiro[5.0.5.4]hexadecan-14-one(CAS DataBase Reference)
NIST Chemistry Reference: (2S,6R,7R,9S,15S)-15-Benzyl-2,9,15-trimethyl-1,8,13,16-tetraoxa-dispiro[5.0.5.4]hexadecan-14-one(155814-63-4)
EPA Substance Registry System: (2S,6R,7R,9S,15S)-15-Benzyl-2,9,15-trimethyl-1,8,13,16-tetraoxa-dispiro[5.0.5.4]hexadecan-14-one(155814-63-4)

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: 155814-63-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 155814-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,8,1 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 155814-63:
(8*1)+(7*5)+(6*5)+(5*8)+(4*1)+(3*4)+(2*6)+(1*3)=144
144 % 10 = 4
So 155814-63-4 is a valid CAS Registry Number.

155814-63-4Upstream product

155814-63-4Downstream Products

155897-76-0 (2S) methyl 2-hydroxy-2-methyl-3-phenylpropanoate

155814-63-4Relevant academic research and scientific papers

Dispiroketals in Synthesis (Part 6): Highly Stereoselective Alkylation of Dispiroketal Protected Lactate and Glycolate Enolates

Downham, Robert,Kim, Kun Soo,Ley, Steven V.,Woods, Martin

, p. 769 - 772 (2007/10/02)

Protected lactic acid enolates have been alkylated with a range of electrophiles to give the substituted adducts with moderate to excellent stereoselectivity.A chiral protected glycolic acid adduct has also been doubly alkylated with high stereoselectivit

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