Cas 74207-05-9,(1S,6S)-6-{[2-(1H-Indol-3-yl)-ethylcarbamoyl]-methyl}-cyclohex-3-enecarboxylic acid methyl ester

74207-05-9

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Basic information

Product Name: (1S,6S)-6-{[2-(1H-Indol-3-yl)-ethylcarbamoyl]-methyl}-cyclohex-3-enecarboxylic acid methyl ester
Synonyms: (1S,6S)-6-{[2-(1H-Indol-3-yl)-ethylcarbamoyl]-methyl}-cyclohex-3-enecarboxylic acid methyl ester
CAS NO:74207-05-9
Molecular Formula:
Molecular Weight: 340.422
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: (1S,6S)-6-{[2-(1H-Indol-3-yl)-ethylcarbamoyl]-methyl}-cyclohex-3-enecarboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (1S,6S)-6-{[2-(1H-Indol-3-yl)-ethylcarbamoyl]-methyl}-cyclohex-3-enecarboxylic acid methyl ester(74207-05-9)
EPA Substance Registry System: (1S,6S)-6-{[2-(1H-Indol-3-yl)-ethylcarbamoyl]-methyl}-cyclohex-3-enecarboxylic acid methyl ester(74207-05-9)

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: 74207-05-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 74207-05-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,2,0 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 74207-05:
(7*7)+(6*4)+(5*2)+(4*0)+(3*7)+(2*0)+(1*5)=109
109 % 10 = 9
So 74207-05-9 is a valid CAS Registry Number.

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74207-05-9Relevant academic research and scientific papers

STUDIES ON THE SYNTHESES OF HETEROCYCLIC AND NATURAL COMPOUNDS. PART 948. A SIMPLE AND CONVENIENT SYNTHESIS OF YOHIMBANE AND ALLOYOHIMBANE

Kametani, Tetsuji,Suzuki, Toshio,Unno, Katsuo

, p. 3819 - 3824 (2007/10/02)

A simple method for the stereoselective synthesis of yohimbane (7) and alloyohimbane (5) via the diazoketone (2) from the anhydride (8), a symmetrical starting material, was examined.The preparation of pentacyclic ring systems contained in yohimbine and r

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