Cas 106375-27-3,3β-chloro-2β-hydroxy-1-<(p-methoxyphenyl)sulfonyl>aspidospermidin-8-one

106375-27-3

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Basic information

Product Name: 3β-chloro-2β-hydroxy-1-<(p-methoxyphenyl)sulfonyl>aspidospermidin-8-one
Synonyms: 3β-chloro-2β-hydroxy-1-<(p-methoxyphenyl)sulfonyl>aspidospermidin-8-one
CAS NO:106375-27-3
Molecular Formula:
Molecular Weight: 517.046
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: 3β-chloro-2β-hydroxy-1-<(p-methoxyphenyl)sulfonyl>aspidospermidin-8-one(CAS DataBase Reference)
NIST Chemistry Reference: 3β-chloro-2β-hydroxy-1-<(p-methoxyphenyl)sulfonyl>aspidospermidin-8-one(106375-27-3)
EPA Substance Registry System: 3β-chloro-2β-hydroxy-1-<(p-methoxyphenyl)sulfonyl>aspidospermidin-8-one(106375-27-3)

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: 106375-27-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 106375-27-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,3,7 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 106375-27:
(8*1)+(7*0)+(6*6)+(5*3)+(4*7)+(3*5)+(2*2)+(1*7)=113
113 % 10 = 3
So 106375-27-3 is a valid CAS Registry Number.

106375-27-3Upstream product

80664-35-3 (+/-)-2,3-didehydro-1-<(p-methoxyphenyl)sulfonyl>aspidospermidin-8-one

106375-27-3Downstream Products

473-99-4 14,15-dihydroeburnamenin-14-ol

106375-27-3Relevant academic research and scientific papers

METHODS FOR INDOLE ALKALOID SYNTHESIS: REACTIONS OF N-ARYLSULFONYLENAMINES WITH ELECTROPHILES. AN EXPEDITIOUS SYNTHESIS OF (+/-)-EBURNAMONINE.

Magnus, Philip,Pappalardo, Paul,Southwell, Ian

, p. 3215 - 3222 (2007/10/02)

Treatment of 4 with MCPBA gave 9.The pentacyclic amide 3 on exposure to cyanogen chloride gave the cis-chloro-hydrin 20, and the geminal dichloride 21.When 21 was treated with HCl/MeOH it rapidly rearranged to eburnamonine lactam 22.

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