Cas 135149-67-6,(1R,2S,3S,4R)-3-Methoxy-2-[(2R,3R)-2-methyl-3-(3-methyl-but-2-enyl)-oxiranyl]-1-phenylsulfanylmethyl-cyclohexane-1,4-diol

135149-67-6

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Basic information

Product Name: (1R,2S,3S,4R)-3-Methoxy-2-[(2R,3R)-2-methyl-3-(3-methyl-but-2-enyl)-oxiranyl]-1-phenylsulfanylmethyl-cyclohexane-1,4-diol
Synonyms: (1R,2S,3S,4R)-3-Methoxy-2-[(2R,3R)-2-methyl-3-(3-methyl-but-2-enyl)-oxiranyl]-1-phenylsulfanylmethyl-cyclohexane-1,4-diol
CAS NO:135149-67-6
Molecular Formula:
Molecular Weight: 392.56
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: (1R,2S,3S,4R)-3-Methoxy-2-[(2R,3R)-2-methyl-3-(3-methyl-but-2-enyl)-oxiranyl]-1-phenylsulfanylmethyl-cyclohexane-1,4-diol(CAS DataBase Reference)
NIST Chemistry Reference: (1R,2S,3S,4R)-3-Methoxy-2-[(2R,3R)-2-methyl-3-(3-methyl-but-2-enyl)-oxiranyl]-1-phenylsulfanylmethyl-cyclohexane-1,4-diol(135149-67-6)
EPA Substance Registry System: (1R,2S,3S,4R)-3-Methoxy-2-[(2R,3R)-2-methyl-3-(3-methyl-but-2-enyl)-oxiranyl]-1-phenylsulfanylmethyl-cyclohexane-1,4-diol(135149-67-6)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 135149-67-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 135149-67-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,1,4 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 135149-67:
(8*1)+(7*3)+(6*5)+(5*1)+(4*4)+(3*9)+(2*6)+(1*7)=126
126 % 10 = 6
So 135149-67-6 is a valid CAS Registry Number.

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135149-67-6Relevant academic research and scientific papers

Fumagalone, a reversible inhibitor of type 2 methionine aminopeptidase and angiogenesis

Zhou, Guochun,Tsai, Chiawei W.,Liu, Jun O.

, p. 3452 - 3454 (2003)

Fumagillin and ovalicin constitute a family of structurally related natural products that possess antiangiogenic activity. We report the synthesis of a new fumagillin analogue, fumagalone, in which the spiroepoxide group is replaced with an aldehyde. Fuma

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