Cas 1002121-41-6,6-methoxy-2,2-dimethyl-1,2,8,8a-tetrahydro-3a-aza-cyclopenta[a]inden-3-one

1002121-41-6

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Basic information

Product Name: 6-methoxy-2,2-dimethyl-1,2,8,8a-tetrahydro-3a-aza-cyclopenta[a]inden-3-one
Synonyms: 6-methoxy-2,2-dimethyl-1,2,8,8a-tetrahydro-3a-aza-cyclopenta[a]inden-3-one
CAS NO:1002121-41-6
Molecular Formula:
Molecular Weight: 231.294
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: 6-methoxy-2,2-dimethyl-1,2,8,8a-tetrahydro-3a-aza-cyclopenta[a]inden-3-one(CAS DataBase Reference)
NIST Chemistry Reference: 6-methoxy-2,2-dimethyl-1,2,8,8a-tetrahydro-3a-aza-cyclopenta[a]inden-3-one(1002121-41-6)
EPA Substance Registry System: 6-methoxy-2,2-dimethyl-1,2,8,8a-tetrahydro-3a-aza-cyclopenta[a]inden-3-one(1002121-41-6)

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: 1002121-41-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1002121-41-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,2,1,2 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1002121-41:
(9*1)+(8*0)+(7*0)+(6*2)+(5*1)+(4*2)+(3*1)+(2*4)+(1*1)=46
46 % 10 = 6
So 1002121-41-6 is a valid CAS Registry Number.

1002121-41-6Upstream product

1002121-20-1 2,2-dimethyl-pent-4-enoic acid (4-methoxy-phenyl)-amide

1002121-41-6Downstream Products

1002121-41-6Relevant academic research and scientific papers

Copper(II) carboxylate-promoted intramolecular carboamination of alkenes for the synthesis of polycyclic lactams

Fuller, Peter H.,Chemler, Sherry R.

, p. 5477 - 5480 (2008/09/17)

The copper(II) carboxylate-promoted intramolecular carboamination reactions of variously substituted y-alkenyl amides have been investigated. These oxidative cyclization reactions efficiently provide polycyclic lactams, useful intermediates in nitrogen he

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