Cas 1445569-75-4,(4R,E)-3-(4-isopropyl-2,3-dimethoxyphenyl)-4-(2-methoxyvinyl)-4,5,5-trimethylcyclohex-2-enone

1445569-75-4

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Basic information

Product Name: (4R,E)-3-(4-isopropyl-2,3-dimethoxyphenyl)-4-(2-methoxyvinyl)-4,5,5-trimethylcyclohex-2-enone
Synonyms: (4R,E)-3-(4-isopropyl-2,3-dimethoxyphenyl)-4-(2-methoxyvinyl)-4,5,5-trimethylcyclohex-2-enone
CAS NO:1445569-75-4
Molecular Formula:
Molecular Weight: 372.505
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: (4R,E)-3-(4-isopropyl-2,3-dimethoxyphenyl)-4-(2-methoxyvinyl)-4,5,5-trimethylcyclohex-2-enone(CAS DataBase Reference)
NIST Chemistry Reference: (4R,E)-3-(4-isopropyl-2,3-dimethoxyphenyl)-4-(2-methoxyvinyl)-4,5,5-trimethylcyclohex-2-enone(1445569-75-4)
EPA Substance Registry System: (4R,E)-3-(4-isopropyl-2,3-dimethoxyphenyl)-4-(2-methoxyvinyl)-4,5,5-trimethylcyclohex-2-enone(1445569-75-4)

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: 1445569-75-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1445569-75-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,5,5,6 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1445569-75:
(9*1)+(8*4)+(7*4)+(6*5)+(5*5)+(4*6)+(3*9)+(2*7)+(1*5)=194
194 % 10 = 4
So 1445569-75-4 is a valid CAS Registry Number.

1445569-75-4Upstream product

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1445569-75-4Relevant academic research and scientific papers

Enantioselective total syntheses of pygmaeocins B and C

Obase, Akiko,Kageyama, Akihito,Manabe, Yuki,Ozawa, Tsukasa,Araki, Takaaki,Yokoe, Hiromasa,Kanematsu, Makoto,Yoshida, Masahiro,Shishido, Kozo

, p. 3666 - 3669 (2013)

The first enantioselective total syntheses of pygmaeocins B and C have been accomplished using an efficient and highly diastereoselective intramolecular Heck cyclization for the construction of a quaternary stereogenic center and the functionalized A-ring of the natural products as the key step.

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