Cas 928258-34-8,3,3-dimethyl-9-((S)-N-methyl-S-phenylsulfonimidoylmethyl)-1,5-dioxaspiro[5.5]undec-8-ene

928258-34-8

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Basic information

Product Name: 3,3-dimethyl-9-((S)-N-methyl-S-phenylsulfonimidoylmethyl)-1,5-dioxaspiro[5.5]undec-8-ene
Synonyms: 3,3-dimethyl-9-((S)-N-methyl-S-phenylsulfonimidoylmethyl)-1,5-dioxaspiro[5.5]undec-8-ene
CAS NO:928258-34-8
Molecular Formula:
Molecular Weight: 349.494
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: 3,3-dimethyl-9-((S)-N-methyl-S-phenylsulfonimidoylmethyl)-1,5-dioxaspiro[5.5]undec-8-ene(CAS DataBase Reference)
NIST Chemistry Reference: 3,3-dimethyl-9-((S)-N-methyl-S-phenylsulfonimidoylmethyl)-1,5-dioxaspiro[5.5]undec-8-ene(928258-34-8)
EPA Substance Registry System: 3,3-dimethyl-9-((S)-N-methyl-S-phenylsulfonimidoylmethyl)-1,5-dioxaspiro[5.5]undec-8-ene(928258-34-8)

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: 928258-34-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 928258-34-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,8,2,5 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 928258-34:
(8*9)+(7*2)+(6*8)+(5*2)+(4*5)+(3*8)+(2*3)+(1*4)=198
198 % 10 = 8
So 928258-34-8 is a valid CAS Registry Number.

928258-34-8Upstream product

928258-34-8Downstream Products

697291-81-9 C₁₀H₁₂ClNO₃S

928258-34-8Relevant academic research and scientific papers

Asymmetric synthesis of substituted homoallyl alcohols, halomethyl tetrahydrofurans, and chloro-amino sulfones from allyltitanium sulfoximines and α-hetero aldehydes

Rajender,Gais, Hans-Joachim

, p. 579 - 582 (2007)

Asymmetric syntheses of the iodomethyl-substituted bicyclic tetrahydrofuran 22 and the chloro-amino sulfone 30 from the allylic sulfoximine 15 and the α-hetero aldehydes 2 and 23, respectively, are described. Further examples for the asymmetric synthesis

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