Cas 298709-72-5,2,2-dimethyl-propionic acid 2-[1-(2,3-dimethoxy-phenyl)-cyclohex-2-enyl]-ethyl ester

298709-72-5

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Basic information

Product Name: 2,2-dimethyl-propionic acid 2-[1-(2,3-dimethoxy-phenyl)-cyclohex-2-enyl]-ethyl ester
Synonyms: 2,2-dimethyl-propionic acid 2-[1-(2,3-dimethoxy-phenyl)-cyclohex-2-enyl]-ethyl ester
CAS NO:298709-72-5
Molecular Formula:
Molecular Weight: 346.467
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-dimethyl-propionic acid 2-[1-(2,3-dimethoxy-phenyl)-cyclohex-2-enyl]-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2,2-dimethyl-propionic acid 2-[1-(2,3-dimethoxy-phenyl)-cyclohex-2-enyl]-ethyl ester(298709-72-5)
EPA Substance Registry System: 2,2-dimethyl-propionic acid 2-[1-(2,3-dimethoxy-phenyl)-cyclohex-2-enyl]-ethyl ester(298709-72-5)

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: 298709-72-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 298709-72-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,8,7,0 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 298709-72:
(8*2)+(7*9)+(6*8)+(5*7)+(4*0)+(3*9)+(2*7)+(1*2)=205
205 % 10 = 5
So 298709-72-5 is a valid CAS Registry Number.

298709-72-5Upstream product

298709-72-5Downstream Products

298709-73-6 2,2-dimethyl-propionic acid 2-[1-(2,3-dimethoxy-phenyl)-4-oxo-cyclohex-2-enyl]-ethyl ester

298709-72-5Relevant academic research and scientific papers

Diastereoselective synthesis of 3,4-dimethoxy-7-morphinanone: A potential route to morphine

Yamada, Osamu,Ogasawara, Kunio

, p. 2785 - 2788 (2007/10/03)

Diastereoselective synthesis of racemic 3,4-dimethoxy-7-morphinanone from racemic 2-(2,3-dimethoxyphenyl)cyclohexen-1-ol has been achieved. The relative structure has been determined by transformation of the product into the known 3,4-dimethoxy-6-morphina

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