Cas 135241-38-2,(5S,9aS)-5-(3,4,5-Trimethoxy-phenyl)-6,7,8,9,9a,10-hexahydro-5H-1,3-dioxa-5a-aza-cyclopenta[b]anthracene

135241-38-2

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Basic information

Product Name: (5S,9aS)-5-(3,4,5-Trimethoxy-phenyl)-6,7,8,9,9a,10-hexahydro-5H-1,3-dioxa-5a-aza-cyclopenta[b]anthracene
Synonyms:
CAS NO:135241-38-2
Molecular Formula:
Molecular Weight: 397.471
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: (5S,9aS)-5-(3,4,5-Trimethoxy-phenyl)-6,7,8,9,9a,10-hexahydro-5H-1,3-dioxa-5a-aza-cyclopenta[b]anthracene(CAS DataBase Reference)
NIST Chemistry Reference: (5S,9aS)-5-(3,4,5-Trimethoxy-phenyl)-6,7,8,9,9a,10-hexahydro-5H-1,3-dioxa-5a-aza-cyclopenta[b]anthracene(135241-38-2)
EPA Substance Registry System: (5S,9aS)-5-(3,4,5-Trimethoxy-phenyl)-6,7,8,9,9a,10-hexahydro-5H-1,3-dioxa-5a-aza-cyclopenta[b]anthracene(135241-38-2)

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: 135241-38-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 135241-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,2,4 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 135241-38:
(8*1)+(7*3)+(6*5)+(5*2)+(4*4)+(3*1)+(2*3)+(1*8)=102
102 % 10 = 2
So 135241-38-2 is a valid CAS Registry Number.

135241-38-2Upstream product

135241-38-2Downstream Products

135241-39-3 4-(5S,9aR)-6,7,8,9,9a,10-Hexahydro-5H-1,3-dioxa-5a-aza-cyclopenta[b]anthracen-5-yl-2,6-dimethoxy-phenol

135241-38-2Relevant academic research and scientific papers

Asymmetric Synthesis XXIV. Benzoquinolizidine Analogues of Podophyllotoxin via CN(R,S) Method.

Lienard, Philippe,Royer, Jacques,Quirion, Jean-Charles,Husson, Henri-Philippe

, p. 2489 - 2492 (2007/10/02)

The alkylation of 2-cyano-6-phenyloxazolopiperidin synthon 1 gave after reduction, the optically active pivotal amine 4.Bischler-Napieralski reaction of different aryl amides derived from 4 furnished the podophyllotoxin analogues 7, 8, and 9 after NaBH4 r

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