Cas 43010-46-4,(S,E)-4-(3,7-dimethyl-3-vinylocta-1,6-dien-1-yl)phenyl acetate

43010-46-4

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Basic information

Product Name: (S,E)-4-(3,7-dimethyl-3-vinylocta-1,6-dien-1-yl)phenyl acetate
Synonyms: (S,E)-4-(3,7-dimethyl-3-vinylocta-1,6-dien-1-yl)phenyl acetate
CAS NO:43010-46-4
Molecular Formula:
Molecular Weight: 298.425
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: (S,E)-4-(3,7-dimethyl-3-vinylocta-1,6-dien-1-yl)phenyl acetate(CAS DataBase Reference)
NIST Chemistry Reference: (S,E)-4-(3,7-dimethyl-3-vinylocta-1,6-dien-1-yl)phenyl acetate(43010-46-4)
EPA Substance Registry System: (S,E)-4-(3,7-dimethyl-3-vinylocta-1,6-dien-1-yl)phenyl acetate(43010-46-4)

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: 43010-46-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 43010-46-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,0,1 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 43010-46:
(7*4)+(6*3)+(5*0)+(4*1)+(3*0)+(2*4)+(1*6)=64
64 % 10 = 4
So 43010-46-4 is a valid CAS Registry Number.

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43010-46-4Relevant academic research and scientific papers

Hypoxia-inducible factor-1 and nuclear factor-κB inhibitory meroterpene analogues of bakuchiol, a constituent of the seeds of Psoralea corylifolia

Wu, Cheng-Zhu,Hong, Seong Su,Cai, Xing Fu,Dat, Nguyen Tien,Nan, Ji-Xing,Hwang, Bang Yeon,Lee, Jung Joon,Lee, Dongho

, p. 2619 - 2623 (2008)

Two new meroterpenoids, 12,13-dihydro-12,13-dihydroxybakuchiol (2) and (12′S)-bisbakuchiol C (3), were isolated from the seeds of Psoralea corylifolia L. (Fabaceae). The structures of 2 and 3 were elucidated by spectroscopic and chemical methods. Six mero

Synthesis and evaluation of bakuchiol derivatives as potential anticancer agents

Wu, Cheng-Zhu,Liu, Da-Chuan,Guo, Xing,Dai, Yiqun,Ma, Tao,Li, Hong-Mei,Huo, Qiang

, (2018/03/09)

A series of bakuchiol derivatives were synthesized and evaluated for their anti-proliferative and the inhibitory activities on SMMC7721 cell line migration using PX-478 as a positive control. The results showed (S,E)-4-(7-methoxy-3,7-dimethyl-3-vinyloct-1

Bakuchiol derivatives as novel and potent cytotoxic agents: A report

Majeed, Rabiya,Reddy, Mallepally V.,Chinthakindi, Praveen K.,Sangwan, Payare L.,Hamid, Abid,Chashoo, Gousia,Saxena, Ajit K.,Koul, Surrinder

experimental part, p. 55 - 67 (2012/04/10)

A library of 28 compounds comprising of acyl, amino, halo, nitro, styryl and cyclized derivatives of bakuchiol have been evaluated against a panel of eight human cancer cell lines. Bioevaluation studies have resulted in the identification of potent cytoto

Novel bisstyryl derivatives of bakuchiol: Targeting oral cavity pathogens

Mallepally V. Reddy,Niranjan Thota,Payare L. Sangwan,Pankaj Malhotra,Furqan Ali,Inshad A. Khan,Swapandeep S. Chimni,Koul, Surrinder

experimental part, p. 3125 - 3134 (2010/09/03)

Novel bisstyryl derivatives of bakuchiol using Heck coupling reaction as the key step were synthesized and screened against a panel of six oral cavity pathogens for their antimicrobial activity. Four compounds (9-12) showed two to fourfold and four to eig

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