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(S,E)-1-(3,7-dimethyl-3-vinylocta-1,6-dien-1-yl)-4-methoxybenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100428-91-9

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100428-91-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100428-91-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,4,2 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 100428-91:
(8*1)+(7*0)+(6*0)+(5*4)+(4*2)+(3*8)+(2*9)+(1*1)=79
79 % 10 = 9
So 100428-91-9 is a valid CAS Registry Number.

100428-91-9Relevant academic research and scientific papers

BIOSYNTHESIS OF BAKUCHIOL, A MEROTERPENE FROM PSORALEA CORYLIFOLIA

Banerji, Asoke,Chintalwar, Gajanan J.

, p. 1945 - 1948 (1983)

Biosynthesis of bakuchiol was examined using phenylalanine and mevalonic acid as substrates.It has been demonstrated that bakuchiol is derived from one phenylpropane (with the loss of one carbon atom) and two isoprenoid (C5) units.Key Word Inde

Enantioselective Synthesis of Quaternary Stereocenters via Chromium Catalysis

Xiong, Yang,Zhang, Guozhu

, p. 5094 - 5097 (2016)

Asymmetric allylation of aldehydes with γ-disubstituted allyl halides has been achieved in the presence of a sulfonamide/oxazoline chromium complex. A variety of synthetically useful α-homoallylic alcohols with two consecutive stereogenic centers, including one quaternary carbon, can be accessed in a highly diastereoselective and enantioselective manner.

Combining Palladium and Chiral Organocatalysis for the Enantioselective Deconjugative Allylation of Enals via Dienamine Intermediates

Hu, Guang,Brenner-Moyer, Stacey E.

, p. 866 - 873 (2022/01/04)

A catalytic enantioselective deconjugative allylation of enals is reported. A variety of enals underwent this transformation in high yield and ee, and products can be readily transformed into γ-allyl enals via a Cope rearrangement without erosion of ee. This transformation was used to install the quaternary stereocenter in (S)-bakuchiol, enabling completion of a concise formal synthesis.

Regioselective molybdenum-catalyzed allylic substitution of tertiary allylic electrophiles: Methodology development and applications

Khan, Ajmal,Khan, Shahid,Salman, Muhammad,Xu, Yaoyao,Zhang, Junjie

, p. 5481 - 5486 (2020/06/10)

The first molybdenum-catalyzed allylic sulfonylation of tertiary allylic electrophiles is described. The method employs a readily accessible catalyst (Mo(CO)6/2,2′-bipyridine, both are commercially available) and represents the first example of the use of a group 6 transition metal-catalyst for allylic sulfonylation of substituted tertiary allylic electrophiles to form carbon-sulfur bonds. This atom economic and operationally simple methodology is characterized by its relatively mild conditions, wide substrate scope, and excellent regioselectivity profile, thus unlocking a new platform to forge sulfone moieties, even in the context of late-stage functionalization and providing ample opportunities for further derivatization through traditional Suzuki cross-coupling reactions.

Synthesis of Chiral Tertiary Boronic Esters: Phosphonate-Directed Catalytic Asymmetric Hydroboration of Trisubstituted Alkenes

Chakrabarty, Suman,Takacs, James M.

, p. 6066 - 6069 (2017/05/09)

Highly enantioselective rhodium-catalyzed hydroboration of allylic phosphonates by pinacolborane affords chiral tertiary boronic esters. The β-borylated phosphonates are readily converted to chiral β- and γ-hydroxyphosphonates and aminophosphonates and to phosphonates bearing a quaternary carbon stereocenter. The utility of the latter is illustrated by the synthesis of (S)-(+)-bakuchiol methyl ether.

Anti-proliferative evaluation of monoterpene derivatives against leukemia

Gautam, Lekh Nath,Ling, Taotao,Lang, Walter,Rivas, Fatima

supporting information, p. 75 - 80 (2016/03/01)

The cure rate of pediatric acute lymphoblastic leukemia (ALL) has significantly improved in the past thirty years, however not all patient cohorts respond well to current chemotherapy regimens. Among the high risk patient cohort is infants with MLL-rearranged (MLL-r) B-ALL, which remains dismal with an overall survival rate 35%. Our program is interested in identifying new molecular scaffolds to better understand the underlying mechanisms and ultimately provide new targeted treatments. Based on a phenotypic screen, phenolic natural products were identified as promising scaffolds for further chemical evaluation. Herein we disclose the effects of a potent anti-proliferative compound 31 against human ALL leukemia cellular models.

A facile asymmetric synthesis of Δ3-2-Hydroxybakuchiol, Bakuchiol and ent-Bakuchiol

Xu, Qian-Qian,Zhao, Qun,Shan, Guang-Sheng,Yang, Xi-Cheng,Shi, Qi-Yuan,Lei, Xinsheng

, p. 10739 - 10746 (2013/12/04)

A facile asymmetric synthesis of Δ3-2-Hydroxybakuchiol, Bakuchiol, and ent-Bakuchiol is described through one common intermediate bearing a chiral all-carbon quaternary carbon center, which involves stereoselectively unconjugated alkylation of the α,β-unsaturated imide bearing Evans' auxiliary, Takai-Utimoto reaction, Negishi reaction, and Heck reaction as key steps.

A short synthesis of (+)-bakuchiol

Esumi, Tomoyuki,Yamamoto, Chihiro,Fukuyama, Yoshiyasu

, p. 1845 - 1847 (2013/09/12)

The concise enantioselective total synthesis of (+)-bakuchiol has been achieved using an asymmetric 1,4-addition to construct its all-carbon chiral quaternary center based on the induction of chirality by the (2′S)-2′-phenyloxazolidinone auxiliary, followed by a one-pot transformation under aldol reaction conditions. The synthesis was completed in four steps from (E)-geranic acid in an overall yield of 53%. Georg Thieme Verlag Stuttgart · New York.

Asymmetric construction of all-carbon quaternary stereocenters by chiral-auxiliary-mediated claisen rearrangement and total synthesis of (+)-Bakuchiol

Takao, Ken-Ichi,Shu, Sakamoto,Touati, Marianne Ayaka,Kusakawa, Yusuke,Tadano, Kin-Ichi

, p. 13330 - 13344 (2013/02/23)

An asymmetric Claisen rearrangement using Oppolzer's camphorsultam was developed. Under thermal conditions, a geraniol-derived substrate underwent the rearrangement with good stereoselectivity. The absolute configuration of the newly formed all-carbon quaternary stereocenter was confirmed by the total synthesis of (+)-bakuchiol from the rearrangement product.

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

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