Cas 398118-91-7,methyl (1R,3S,2'S,4'R,5'R)-1-(5'-benzoylamino-4'-methyl-1',3'-dioxane-2'-yl)-methyl-1,2,3,4-tetrahydrocarboline-3-carboxylate

398118-91-7

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Basic information

Product Name: methyl (1R,3S,2'S,4'R,5'R)-1-(5'-benzoylamino-4'-methyl-1',3'-dioxane-2'-yl)-methyl-1,2,3,4-tetrahydrocarboline-3-carboxylate
Synonyms: methyl (1R,3S,2'S,4'R,5'R)-1-(5'-benzoylamino-4'-methyl-1',3'-dioxane-2'-yl)-methyl-1,2,3,4-tetrahydrocarboline-3-carboxylate
CAS NO:398118-91-7
Molecular Formula:
Molecular Weight: 463.533
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: methyl (1R,3S,2'S,4'R,5'R)-1-(5'-benzoylamino-4'-methyl-1',3'-dioxane-2'-yl)-methyl-1,2,3,4-tetrahydrocarboline-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (1R,3S,2'S,4'R,5'R)-1-(5'-benzoylamino-4'-methyl-1',3'-dioxane-2'-yl)-methyl-1,2,3,4-tetrahydrocarboline-3-carboxylate(398118-91-7)
EPA Substance Registry System: methyl (1R,3S,2'S,4'R,5'R)-1-(5'-benzoylamino-4'-methyl-1',3'-dioxane-2'-yl)-methyl-1,2,3,4-tetrahydrocarboline-3-carboxylate(398118-91-7)

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: 398118-91-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 398118-91-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,8,1,1 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 398118-91:
(8*3)+(7*9)+(6*8)+(5*1)+(4*1)+(3*8)+(2*9)+(1*1)=187
187 % 10 = 7
So 398118-91-7 is a valid CAS Registry Number.

398118-91-7Upstream product

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398118-91-7Relevant academic research and scientific papers

Diasteroselective cyclizations with enantiopure malonaldehyde monocycloacetals

Bi, Lanrong,Zhao, Ming,Wang, Chao,Peng, Shiqi,Winterfeldt, Ekkehard

, p. 22 - 26 (2007/10/03)

The synthesis of a series of enantiopure malonaldehyde monocycloacetals is described. Treatment of 8b with L-tryptophan methyl ester, 5-methoxytryptamine, and tryptamine, respectively, in the Pictet-Spengler condensation gave the corresponding enantiomerically pure key precursors 1-3 and 17-21 in only two steps. Using a chiral amino-diol successfully realized the kinetic resolution of racemic carbolines 23 and 24.

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