Cas 1004513-72-7,(1R)-N-[(1R)-1-phenylethyl]-2,3,4,9-tetrahydro-1H-β-carboline-1-carboxamide

1004513-72-7

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Basic information

Product Name: (1R)-N-[(1R)-1-phenylethyl]-2,3,4,9-tetrahydro-1H-β-carboline-1-carboxamide
Synonyms:
CAS NO:1004513-72-7
Molecular Formula:
Molecular Weight: 319.406
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: (1R)-N-[(1R)-1-phenylethyl]-2,3,4,9-tetrahydro-1H-β-carboline-1-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: (1R)-N-[(1R)-1-phenylethyl]-2,3,4,9-tetrahydro-1H-β-carboline-1-carboxamide(1004513-72-7)
EPA Substance Registry System: (1R)-N-[(1R)-1-phenylethyl]-2,3,4,9-tetrahydro-1H-β-carboline-1-carboxamide(1004513-72-7)

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: 1004513-72-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1004513-72-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,4,5,1 and 3 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1004513-72:
(9*1)+(8*0)+(7*0)+(6*4)+(5*5)+(4*1)+(3*3)+(2*7)+(1*2)=87
87 % 10 = 7
So 1004513-72-7 is a valid CAS Registry Number.

1004513-72-7Upstream product

1004513-65-8 C₂₀H₂₁N₃O₂

1004513-72-7Downstream Products

1004513-72-7Relevant academic research and scientific papers

(R)-1-Phenylethylamine as chiral auxiliary in the diastereoselective synthesis of tetrahydro-β-carboline derivatives

Siwicka, Aleksandra,Wojtasiewicz, Krystyna,Leniewski, Andrzej,Maurin, Jan K.,Zawadzka, Anna,Czarnocki, Zbigniew

, p. 1033 - 1036 (2007)

Modified sodium borohydrides were used in the reduction of the imine moiety in compounds containing the (R)-1-arylethylamine motif as a chiral auxiliary. Diastereomeric products were formed with moderate to good stereoselectivity and were effectively sepa

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