Cas 1067236-41-2,(3S,5S,6R,7aS)-3-(1,3-benzodioxol-5-yl)-5-benzyloxy-1-[(4-methylphenyl)sulfonyl]-2,3,5,6,7,7a-hexahydro-1H-6-indolol

1067236-41-2

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Basic information

Product Name: (3S,5S,6R,7aS)-3-(1,3-benzodioxol-5-yl)-5-benzyloxy-1-[(4-methylphenyl)sulfonyl]-2,3,5,6,7,7a-hexahydro-1H-6-indolol
Synonyms: (3S,5S,6R,7aS)-3-(1,3-benzodioxol-5-yl)-5-benzyloxy-1-[(4-methylphenyl)sulfonyl]-2,3,5,6,7,7a-hexahydro-1H-6-indolol
CAS NO:1067236-41-2
Molecular Formula:
Molecular Weight: 519.618
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: (3S,5S,6R,7aS)-3-(1,3-benzodioxol-5-yl)-5-benzyloxy-1-[(4-methylphenyl)sulfonyl]-2,3,5,6,7,7a-hexahydro-1H-6-indolol(CAS DataBase Reference)
NIST Chemistry Reference: (3S,5S,6R,7aS)-3-(1,3-benzodioxol-5-yl)-5-benzyloxy-1-[(4-methylphenyl)sulfonyl]-2,3,5,6,7,7a-hexahydro-1H-6-indolol(1067236-41-2)
EPA Substance Registry System: (3S,5S,6R,7aS)-3-(1,3-benzodioxol-5-yl)-5-benzyloxy-1-[(4-methylphenyl)sulfonyl]-2,3,5,6,7,7a-hexahydro-1H-6-indolol(1067236-41-2)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
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Hazardous Substances Data: 1067236-41-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1067236-41-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,7,2,3 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1067236-41:
(9*1)+(8*0)+(7*6)+(6*7)+(5*2)+(4*3)+(3*6)+(2*4)+(1*1)=142
142 % 10 = 2
So 1067236-41-2 is a valid CAS Registry Number.

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1067236-41-2Relevant academic research and scientific papers

An expedient route to montanine-type amaryllidaceae alkaloids: Total syntheses of (-)-brunsvigine and (-)-manthine

Hong, An-Wei,Cheng, Tsung-Hui,Raghukumar, Vellingiri,Sha, Chin-Kang

, p. 7580 - 7585 (2008/12/22)

(Chemical Equation Presented) The first total syntheses of (-)-brunsvigine (1) and (-)-manthine (2) were accomplished in 10 and 18 steps, respectively. (-)-Quinic acid was converted to enone 12 in live steps. Iodination of enone 12 followed by stereoselec

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