Cas 94061-32-2,(4E,5S)-4-ethylidene-6-methyl-1,3,4,5,6,7-hexahydro-2,5-ethanoazocino[4,3-b]indol-6-ol

94061-32-2

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Basic information

Product Name: (4E,5S)-4-ethylidene-6-methyl-1,3,4,5,6,7-hexahydro-2,5-ethanoazocino[4,3-b]indol-6-ol
Synonyms:
CAS NO:94061-32-2
Molecular Formula: C₁₈H₂₂N₂O
Molecular Weight: 282.3801
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: 458.1°C at 760 mmHg
Flash Point: 230.8°C
Appearance: N/A
Density: 1.24g/cm³
Vapor Pressure: 3.48E-09mmHg at 25°C
Refractive Index: 1.675
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (4E,5S)-4-ethylidene-6-methyl-1,3,4,5,6,7-hexahydro-2,5-ethanoazocino[4,3-b]indol-6-ol(CAS DataBase Reference)
NIST Chemistry Reference: (4E,5S)-4-ethylidene-6-methyl-1,3,4,5,6,7-hexahydro-2,5-ethanoazocino[4,3-b]indol-6-ol(94061-32-2)
EPA Substance Registry System: (4E,5S)-4-ethylidene-6-methyl-1,3,4,5,6,7-hexahydro-2,5-ethanoazocino[4,3-b]indol-6-ol(94061-32-2)

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: 94061-32-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 94061-32-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,0,6 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 94061-32:
(7*9)+(6*4)+(5*0)+(4*6)+(3*1)+(2*3)+(1*2)=122
122 % 10 = 2
So 94061-32-2 is a valid CAS Registry Number.

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94061-32-2Relevant academic research and scientific papers

Structure determination and total synthesis of (+)-16-hydroxy-16,22- dihydroapparicine

Hirose, Tomoyasu,Noguchi, Yoshihiko,Furuya, Yujiro,Ishiyama, Aki,Iwatsuki, Masato,Otoguro, Kazuhiko,Omura, Satoshi,Sunazuka, Toshiaki

, p. 10741 - 10750 (2013)

Herein, we describe the first asymmetric total synthesis and determination of the relative and absolute stereochemistry of naturally occurring 16-hydroxy-16,22-dihydroapparicine. The key steps include 1) a novel phosphinimine-mediated cascade reaction to

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