Cas 494838-83-4,2-[2-(2-chloro-ethyl)-4,5-dimethoxy-phenyl]-3-methyl-cyclopent-2-enone

494838-83-4

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Basic information

Product Name: 2-[2-(2-chloro-ethyl)-4,5-dimethoxy-phenyl]-3-methyl-cyclopent-2-enone
Synonyms: 2-[2-(2-chloro-ethyl)-4,5-dimethoxy-phenyl]-3-methyl-cyclopent-2-enone
CAS NO:494838-83-4
Molecular Formula:
Molecular Weight: 294.778
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: 2-[2-(2-chloro-ethyl)-4,5-dimethoxy-phenyl]-3-methyl-cyclopent-2-enone(CAS DataBase Reference)
NIST Chemistry Reference: 2-[2-(2-chloro-ethyl)-4,5-dimethoxy-phenyl]-3-methyl-cyclopent-2-enone(494838-83-4)
EPA Substance Registry System: 2-[2-(2-chloro-ethyl)-4,5-dimethoxy-phenyl]-3-methyl-cyclopent-2-enone(494838-83-4)

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: 494838-83-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 494838-83-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,4,8,3 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 494838-83:
(8*4)+(7*9)+(6*4)+(5*8)+(4*3)+(3*8)+(2*8)+(1*3)=214
214 % 10 = 4
So 494838-83-4 is a valid CAS Registry Number.

494838-83-4Upstream product

494838-83-4Downstream Products

480445-13-4 2-[2-(2-azido-ethyl)-4,5-dimethoxy-phenyl]-3-methyl-cyclopent-2-enone

494838-83-4Relevant academic research and scientific papers

Thermal rearrangements of α-(ω-azidoalkyl) enones

Molander, Gary A.,Bibeau, Christopher T.

, p. 5385 - 5388 (2002)

The thermal rearrangement of α-(ω-azidoalkyl) enones has been investigated. A variety of these substrates were synthesized and subjected to thermal rearrangement to investigate the scope and generality of their transformation to bicyclic lactams.

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