Cas 148409-72-7,(E)-(S)-4-[(2S,3S,6S)-6-((R)-2-Benzyloxy-1-methyl-ethyl)-3-methyl-tetrahydro-pyran-2-yl]-2-methyl-pent-3-en-1-ol

148409-72-7

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Basic information

Product Name: (E)-(S)-4-[(2S,3S,6S)-6-((R)-2-Benzyloxy-1-methyl-ethyl)-3-methyl-tetrahydro-pyran-2-yl]-2-methyl-pent-3-en-1-ol
Synonyms:
CAS NO:148409-72-7
Molecular Formula:
Molecular Weight: 346.51
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: (E)-(S)-4-[(2S,3S,6S)-6-((R)-2-Benzyloxy-1-methyl-ethyl)-3-methyl-tetrahydro-pyran-2-yl]-2-methyl-pent-3-en-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: (E)-(S)-4-[(2S,3S,6S)-6-((R)-2-Benzyloxy-1-methyl-ethyl)-3-methyl-tetrahydro-pyran-2-yl]-2-methyl-pent-3-en-1-ol(148409-72-7)
EPA Substance Registry System: (E)-(S)-4-[(2S,3S,6S)-6-((R)-2-Benzyloxy-1-methyl-ethyl)-3-methyl-tetrahydro-pyran-2-yl]-2-methyl-pent-3-en-1-ol(148409-72-7)

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: 148409-72-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 148409-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,4,0 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 148409-72:
(8*1)+(7*4)+(6*8)+(5*4)+(4*0)+(3*9)+(2*7)+(1*2)=147
147 % 10 = 7
So 148409-72-7 is a valid CAS Registry Number.

148409-72-7Upstream product

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148409-72-7Relevant academic research and scientific papers

Synthetic studies of the ionophore antibiotic zincophorin. 2. Iterative sigmatropic construction of the C1-C11 subunit

Cywin, Charles L.,Kallmerten, James

, p. 1103 - 1106 (2007/10/02)

Advanced intermediates 22 and 23, representing the C1-C11 subunit of the ionophore zincophorin, have been prepared by a scheme incorporating sequential glycolate Claisen and [2,3] Wittig rearrangements to establish the key structural

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