Cas 207920-74-9,[(1S,2S)-1-((S)-2-Benzyloxy-1-methyl-ethyl)-2-methyl-but-3-enyloxy]-tert-butyl-dimethyl-silane

207920-74-9

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Basic information

Product Name: [(1S,2S)-1-((S)-2-Benzyloxy-1-methyl-ethyl)-2-methyl-but-3-enyloxy]-tert-butyl-dimethyl-silane
Synonyms: [(1S,2S)-1-((S)-2-Benzyloxy-1-methyl-ethyl)-2-methyl-but-3-enyloxy]-tert-butyl-dimethyl-silane
CAS NO:207920-74-9
Molecular Formula:
Molecular Weight: 348.601
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: [(1S,2S)-1-((S)-2-Benzyloxy-1-methyl-ethyl)-2-methyl-but-3-enyloxy]-tert-butyl-dimethyl-silane(CAS DataBase Reference)
NIST Chemistry Reference: [(1S,2S)-1-((S)-2-Benzyloxy-1-methyl-ethyl)-2-methyl-but-3-enyloxy]-tert-butyl-dimethyl-silane(207920-74-9)
EPA Substance Registry System: [(1S,2S)-1-((S)-2-Benzyloxy-1-methyl-ethyl)-2-methyl-but-3-enyloxy]-tert-butyl-dimethyl-silane(207920-74-9)

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: 207920-74-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 207920-74-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,9,2 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 207920-74:
(8*2)+(7*0)+(6*7)+(5*9)+(4*2)+(3*0)+(2*7)+(1*4)=129
129 % 10 = 9
So 207920-74-9 is a valid CAS Registry Number.

207920-74-9Upstream product

207920-74-9Downstream Products

207920-74-9Relevant academic research and scientific papers

Improved Synthesis of the C8-C23 Segment of Aplysiatoxins via Asymmetric Dihydroxylation of the Chiral Homoallylic Alcohol

Toshima, Hiroaki,Ichihara, Akitami

, p. 599 - 602 (2007/10/03)

Important intermediate 2 of the segment (3) possessing four sequential asymmetric centers (C9-C12) of aplysiatoxins was synthesized via dihydroxylation of 5 in only 7 steps from methyl (S)-3-hydroxy-2-methylpropionate.Another promising compound (10a) was

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