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4-(3,5-dibromo-4-methoxybenzylidene)-2-methyloxazol-5(4H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

346633-39-4

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346633-39-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 346633-39-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,6,6,3 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 346633-39:
(8*3)+(7*4)+(6*6)+(5*6)+(4*3)+(3*3)+(2*3)+(1*9)=154
154 % 10 = 4
So 346633-39-4 is a valid CAS Registry Number.

346633-39-4Relevant academic research and scientific papers

Synthesis and antiproliferative activity of marine bromotyrosine purpurealidin I and its derivatives

Bhat, Chinmay,Ilina, Polina,Tilli, Irene,Vorá?ová, Manuela,Bruun, Tanja,Barba, Victoria,Hribernik, Nives,Lillsunde, Katja-Emilia,M?ki-Lohiluoma, Eero,Rüffer, Tobias,Lang, Heinrich,Yli-Kauhaluoma, Jari,Kiuru, Paula,Tammela, P?ivi

, (2018)

The first total synthesis of the marine bromotyrosine purpurealidin I (1) using trifluoroacetoxy protection group and its dimethylated analog (29) is reported along with 16 simplified bromotyrosine derivatives lacking the tyramine moiety. Their cytotoxici

A natural product spermatinamine derivative and its preparation and use (by machine translation)

-

, (2017/08/08)

The invention belongs to the technical field of pharmaceutical and chemical industry, discloses a natural product of the alkaloid derivatives of spermatinamine design and its synthetic method and its application of antibacterial on. In the present inventi

An improved total synthesis of spermatinamine, an inhibitor of isoprenylcysteine carboxy methyltransferase

Ullah, Nisar,Haladu, Shamsuddeen A.,Mosa, Basem A.

experimental part, p. 212 - 214 (2011/02/26)

An improved total synthesis of spermatinamine, an inhibitor of the anticancer target, isoprenylcysteine carboxy methyltransferase (Icmt) was accomplished from the commercially available 3,4-dibromo-4-hydroxybenzaldehyde via a high yielding reaction sequen

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