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tert-butyl (2-{4-[5-(2-aminoethyl)-3-bromo-2-hydroxyphenoxy]-3,5-dibromophenyl}ethyl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

210880-82-3

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210880-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 210880-82-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,8,8 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 210880-82:
(8*2)+(7*1)+(6*0)+(5*8)+(4*8)+(3*0)+(2*8)+(1*2)=113
113 % 10 = 3
So 210880-82-3 is a valid CAS Registry Number.

210880-82-3Downstream Products

210880-82-3Relevant academic research and scientific papers

Efficient total synthesis of bastadin 6, an anti-angiogenic brominated tyrosine-derived metabolite from marine sponge

Kotoku, Naoyuki,Tsujita, Hiroaki,Hiramatsu, Atsushi,Mori, Chinatsu,Koizumi, Noriko,Kobayashi, Motomasa

, p. 7211 - 7218 (2007/10/03)

An efficient total synthesis of bastadin 6 (1), a cyclic tetramer of brominated tyrosine derivatives from the marine sponge, Ianthella basta, with selective anti-angiogenic activity, was accomplished. We developed a novel Ce(IV)-mediated oxidative couplin

Total synthesis of bastadins 2, 3, and 6

Guo, Zhi-Wei,Machiya, Koji,Salamonczyk, Grzegorz M.,Sih, Charles J.

, p. 4269 - 4276 (2007/10/03)

A chemoenzymatic strategy has been developed for the synthesis of bastadins 2, 3, and 6. The requisite dimeric dityrosine and isodityrosine building blocks were successfully prepared by oxidative C - C and C - O phenolic coupling of mono- and dihalogenated derivatives of tyrosine and tyramine using horseradish and soybean peroxidases. By carefully controlling the experimental parameters, the requisite synthons may now be prepared in synthetically useful yields without the exhaustive protection and deprotection of the sensitive functional groups.

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