Cas 76579-70-9,(Z)-4-[1-[4-(2-dimethylamino-ethoxy)-phenyl]-4-methyl-2-phenyl-pent-1-enyl]phenol

76579-70-9

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Basic information

Product Name: (Z)-4-[1-[4-(2-dimethylamino-ethoxy)-phenyl]-4-methyl-2-phenyl-pent-1-enyl]phenol
Synonyms: (Z)-4-[1-[4-(2-dimethylamino-ethoxy)-phenyl]-4-methyl-2-phenyl-pent-1-enyl]phenol
CAS NO:76579-70-9
Molecular Formula:
Molecular Weight: 401.549
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: (Z)-4-[1-[4-(2-dimethylamino-ethoxy)-phenyl]-4-methyl-2-phenyl-pent-1-enyl]phenol(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-4-[1-[4-(2-dimethylamino-ethoxy)-phenyl]-4-methyl-2-phenyl-pent-1-enyl]phenol(76579-70-9)
EPA Substance Registry System: (Z)-4-[1-[4-(2-dimethylamino-ethoxy)-phenyl]-4-methyl-2-phenyl-pent-1-enyl]phenol(76579-70-9)

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: 76579-70-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 76579-70-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,5,7 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 76579-70:
(7*7)+(6*6)+(5*5)+(4*7)+(3*9)+(2*7)+(1*0)=179
179 % 10 = 9
So 76579-70-9 is a valid CAS Registry Number.

76579-70-9Upstream product

76579-70-9Downstream Products

76579-70-9Relevant academic research and scientific papers

Identification of novel inverse agonists of estrogen-related receptors ERRγ and ERRβ

Yu, Donna D.,Huss, Janice M.,Li, Hongzhi,Forman, Barry M.

, p. 1585 - 1599 (2017)

Estrogen-related receptors (ERRs, α, β, and γ) are orphan nuclear receptors most closely related in sequence to estrogen receptors (ERα and ERβ). Much attention has been paid recently to the functions of ERRs for their potential roles as new therapeutic t

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