Cas 370866-99-2,dithiocarbonic acid S-(cyclohex-2-enylmethyl-N-[2-(1H-indol-3-yl)ethyl]-carbamoyl)methyl O-ethyl ester

370866-99-2

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Basic information

Product Name: dithiocarbonic acid S-(cyclohex-2-enylmethyl-N-[2-(1H-indol-3-yl)ethyl]-carbamoyl)methyl O-ethyl ester
Synonyms: dithiocarbonic acid S-(cyclohex-2-enylmethyl-N-[2-(1H-indol-3-yl)ethyl]-carbamoyl)methyl O-ethyl ester
CAS NO:370866-99-2
Molecular Formula:
Molecular Weight: 416.609
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: dithiocarbonic acid S-(cyclohex-2-enylmethyl-N-[2-(1H-indol-3-yl)ethyl]-carbamoyl)methyl O-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: dithiocarbonic acid S-(cyclohex-2-enylmethyl-N-[2-(1H-indol-3-yl)ethyl]-carbamoyl)methyl O-ethyl ester(370866-99-2)
EPA Substance Registry System: dithiocarbonic acid S-(cyclohex-2-enylmethyl-N-[2-(1H-indol-3-yl)ethyl]-carbamoyl)methyl O-ethyl ester(370866-99-2)

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: 370866-99-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 370866-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,0,8,6 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 370866-99:
(8*3)+(7*7)+(6*0)+(5*8)+(4*6)+(3*6)+(2*9)+(1*9)=182
182 % 10 = 2
So 370866-99-2 is a valid CAS Registry Number.

370866-99-2Upstream product

370866-99-2Downstream Products

10283-63-3 2-[2-(1H-indol-3-yl)ethyl]octahydroisoquinolin-3-one

370866-99-2Relevant academic research and scientific papers

An easy entry into berbane and alloyohimbane alkaloids via a 6-exo radical cyclization

Kaoudi, Talbi,Miranda, Luis D.,Zard, Samir Z.

, p. 3125 - 3127 (2007/10/03)

(formula presented) The pharmacologically important tetracyclic berbane and pentacyclic alloyohimbane structures were prepared efficiently in four steps including a stereoselective 6-exo radical cyclization using xanthates as the radical source.

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