Cas 1334535-28-2,(4aR,7aR,12bR)-10-fluoro-3-tosyl-1,2,3,4,4a,5,7a,8-octahydropyrido[3,4-d]carbazol-6(7H)-one

1334535-28-2

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Basic information

Product Name: (4aR,7aR,12bR)-10-fluoro-3-tosyl-1,2,3,4,4a,5,7a,8-octahydropyrido[3,4-d]carbazol-6(7H)-one
Synonyms: (4aR,7aR,12bR)-10-fluoro-3-tosyl-1,2,3,4,4a,5,7a,8-octahydropyrido[3,4-d]carbazol-6(7H)-one
CAS NO:1334535-28-2
Molecular Formula:
Molecular Weight: 414.501
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: (4aR,7aR,12bR)-10-fluoro-3-tosyl-1,2,3,4,4a,5,7a,8-octahydropyrido[3,4-d]carbazol-6(7H)-one(CAS DataBase Reference)
NIST Chemistry Reference: (4aR,7aR,12bR)-10-fluoro-3-tosyl-1,2,3,4,4a,5,7a,8-octahydropyrido[3,4-d]carbazol-6(7H)-one(1334535-28-2)
EPA Substance Registry System: (4aR,7aR,12bR)-10-fluoro-3-tosyl-1,2,3,4,4a,5,7a,8-octahydropyrido[3,4-d]carbazol-6(7H)-one(1334535-28-2)

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: 1334535-28-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1334535-28-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,4,5,3 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1334535-28:
(9*1)+(8*3)+(7*3)+(6*4)+(5*5)+(4*3)+(3*5)+(2*2)+(1*8)=142
142 % 10 = 2
So 1334535-28-2 is a valid CAS Registry Number.

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1334535-28-2Relevant academic research and scientific papers

Enantioselective Michael/Mannich polycyclization cascade of indolyl enones catalyzed by quinine-derived primary amines

Cai, Quan,Zheng, Chao,Zhang, Jun-Wei,You, Shu-Li

supporting information; experimental part, p. 8665 - 8669 (2011/11/06)

Three's a crowd: The title reaction provides a tetracylic core bearing three chiral centers (see scheme; Ts=4-toluenesulfonyl) with excellent enantioselectivity and good diastereoselectivity. The reaction was used to efficiently construct the (+)-kreysigi

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