Cas 1221716-69-3,dimethyl-2-(3-fluorophenyl)-3-formyl-4-methylcyclopent-3-ene-1,1-dicarboxylate

1221716-69-3

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Basic information

Product Name: dimethyl-2-(3-fluorophenyl)-3-formyl-4-methylcyclopent-3-ene-1,1-dicarboxylate
Synonyms: dimethyl-2-(3-fluorophenyl)-3-formyl-4-methylcyclopent-3-ene-1,1-dicarboxylate
CAS NO:1221716-69-3
Molecular Formula:
Molecular Weight: 320.317
EINECS: N/A
Product Categories: N/A
Mol File: 1221716-69-3.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: dimethyl-2-(3-fluorophenyl)-3-formyl-4-methylcyclopent-3-ene-1,1-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: dimethyl-2-(3-fluorophenyl)-3-formyl-4-methylcyclopent-3-ene-1,1-dicarboxylate(1221716-69-3)
EPA Substance Registry System: dimethyl-2-(3-fluorophenyl)-3-formyl-4-methylcyclopent-3-ene-1,1-dicarboxylate(1221716-69-3)

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: 1221716-69-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1221716-69-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,1,7,1 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1221716-69:
(9*1)+(8*2)+(7*2)+(6*1)+(5*7)+(4*1)+(3*6)+(2*6)+(1*9)=123
123 % 10 = 3
So 1221716-69-3 is a valid CAS Registry Number.

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1221716-69-3Relevant articles and documents

Highly enantioselective Michael-cyclization cascade promoted by synergistic asymmetric aminocatalysis and Lewis acid catalysis

Yu, Chenguang,Zhang, Yinan,Zhang, Shilei,He, Jing,Wang, Wei

supporting information; experimental part, p. 1742 - 1744 (2010/05/18)

The novel dual cooperative asymmetric aminocatalysis and Lewis acid catalysis has been successfully developed for promoting cascade Michael-cyclization reaction with high enantio-, regio- and chemo-selectivity. The simple and practical process affords a one-pot approach to synthetically useful cyclopentenes.

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