Cas 943229-15-0,N-[2-(3,4-dimethoxyphenyl)cyclohexen-1-yl]-N-methyl-α-(methylthio)acetamide

943229-15-0

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Basic information

Product Name: N-[2-(3,4-dimethoxyphenyl)cyclohexen-1-yl]-N-methyl-α-(methylthio)acetamide
Synonyms: N-[2-(3,4-dimethoxyphenyl)cyclohexen-1-yl]-N-methyl-α-(methylthio)acetamide
CAS NO:943229-15-0
Molecular Formula:
Molecular Weight: 335.467
EINECS: N/A
Product Categories: N/A
Mol File: 943229-15-0.mol
Article Data: 1

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: N-[2-(3,4-dimethoxyphenyl)cyclohexen-1-yl]-N-methyl-α-(methylthio)acetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[2-(3,4-dimethoxyphenyl)cyclohexen-1-yl]-N-methyl-α-(methylthio)acetamide(943229-15-0)
EPA Substance Registry System: N-[2-(3,4-dimethoxyphenyl)cyclohexen-1-yl]-N-methyl-α-(methylthio)acetamide(943229-15-0)

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: 943229-15-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 943229-15-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,2,2 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 943229-15:
(8*9)+(7*4)+(6*3)+(5*2)+(4*2)+(3*9)+(2*1)+(1*5)=170
170 % 10 = 0
So 943229-15-0 is a valid CAS Registry Number.

943229-15-0Upstream product

943229-15-0Downstream Products

510-80-5 (3aS^*,7aS^*)-3a-(3,4-dimethoxyphenyl)-1-methyloctahydroindole

943229-15-0Relevant articles and documents

Stereoselective synthesis of cis and trans-fused 3a-aryloctahydroindoles using cyclization of N-vinylic α-(methylthio)acetamides: synthesis of (-)-mesembrane

Saito, Miho,Matsuo, Jun-ichi,Ishibashi, Hiroyuki

, p. 4865 - 4873 (2007)

Treatment of N-(2-arylcyclohex-1-en-1-yl)-α-(methylthio)acetamides with N-chlorosuccinimide (NCS) gave 3a-aryl-2,3,3a,4,5,6-hexahydro-3-(methylthio)indol-2-ones. Desulfurization of the cyclization products followed by a catalytic hydrogenation of the resu

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