Cas 113180-49-7,(+/-)-1-<(4-methylphenyl)sulfonyl>-4-<3-methyl-1-<<2-(trimethylsilyl)ethoxy>methoxy>-2-butenyl>-1H-indole

113180-49-7

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Basic information

Product Name: (+/-)-1-<(4-methylphenyl)sulfonyl>-4-<3-methyl-1-<<2-(trimethylsilyl)ethoxy>methoxy>-2-butenyl>-1H-indole
Synonyms: (+/-)-1-<(4-methylphenyl)sulfonyl>-4-<3-methyl-1-<<2-(trimethylsilyl)ethoxy>methoxy>-2-butenyl>-1H-indole
CAS NO:113180-49-7
Molecular Formula:
Molecular Weight: 485.72
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: (+/-)-1-<(4-methylphenyl)sulfonyl>-4-<3-methyl-1-<<2-(trimethylsilyl)ethoxy>methoxy>-2-butenyl>-1H-indole(CAS DataBase Reference)
NIST Chemistry Reference: (+/-)-1-<(4-methylphenyl)sulfonyl>-4-<3-methyl-1-<<2-(trimethylsilyl)ethoxy>methoxy>-2-butenyl>-1H-indole(113180-49-7)
EPA Substance Registry System: (+/-)-1-<(4-methylphenyl)sulfonyl>-4-<3-methyl-1-<<2-(trimethylsilyl)ethoxy>methoxy>-2-butenyl>-1H-indole(113180-49-7)

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: 113180-49-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 113180-49-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,1,8 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 113180-49:
(8*1)+(7*1)+(6*3)+(5*1)+(4*8)+(3*0)+(2*4)+(1*9)=87
87 % 10 = 7
So 113180-49-7 is a valid CAS Registry Number.

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113180-49-7Relevant academic research and scientific papers

Probing ergot alkaloid biosynthesis: Intermediates in the formation of ring C

Kozikowski, Alan P.,Chen, Chinpiao,Wu, Jiang-Ping,Shibuya, Masaaki,Kim, Chun-Gyu,Floss, Heinz G.

, p. 2482 - 2488 (2007/10/02)

The mode of C-ring formation in ergot alkaloid biosynthesis was probed by synthesizing two potential intermediates, compounds 6 and 7, in deuterated form from the prenylated indole 8. Both compounds were incorporated into the ergot alkaloid elymoclavine b

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