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{tert-butoxycarbonylmethyl-[1-hydroxymethyl-4-(4-nitrophenyl)butyl]amino}acetic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1142811-83-3

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1142811-83-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1142811-83-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,2,8,1 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1142811-83:
(9*1)+(8*1)+(7*4)+(6*2)+(5*8)+(4*1)+(3*1)+(2*8)+(1*3)=123
123 % 10 = 3
So 1142811-83-3 is a valid CAS Registry Number.

1142811-83-3Relevant academic research and scientific papers

Bimodal ligands with macrocyclic and acyclic binding moieties, complexes and compositions thereof, and methods of using

-

, (2015/09/23)

Substituted 1,4,7-triazacyclononane-N,N′,N″-triacetic acid and 1,4,7,10-tetraazacyclcododecane-N,N′,N″,N′″-tetraacetic acid compounds with a pendant amino or hydroxyl group, metal complexes thereof, compositions thereof, and methods of making and use in diagnostic imaging and treatment of cellular disorders.

A highly effective bifunctional ligand for radioimmunotherapy applications

Chong, Hyun-Soon,Song, Hyun A.,Kang, Chi Soo,Le, Thien,Sun, Xiang,Dadwal, Mamta,Lee, Hyunbeom,Lan, Xiaoli,Chen, Yunwei,Dai, Anzhi

, p. 5584 - 5586 (2011/06/21)

A novel bifunctional ligand (3p-C-NETA) for antibody-targeted radioimmunotherapy (RIT) of β-emitting radioisotopes 90Y and 177Lu was efficiently synthesized via an unexpected regiospecific ring opening of an aziridinium ion. 3p-C-NET

Bimodal ligands with macrocyclic and acyclic binding moieties, complexes and compositions thereof, and methods of using

-

, (2010/12/31)

Substituted 1,4,7-triazacyclononane-N,N′,N″-triacetic acid and 1,4,7,10-tetraazacyclcododecane-N,N′,N″,N′″-tetraacetic acid compounds with a pendant amino or hydroxyl group, metal complexes thereof, compositions thereof, and methods of making and use in diagnostic imaging and treatment of cellular disorders.

Stable aziridinium salts as versatile intermediates: Isolation and regio- and stereoselective ring-opening and rearrangement

Song, Hyun A.,Dadwal, Mamta,Lee, Yeseul,Mick, Emily,Chong, Hyun-Soon

supporting information; experimental part, p. 1328 - 1330 (2009/06/30)

Rock trapping and exploration: Aziridinium bromide salts were discovered serendipitously during bromination of N,N-dicarboxymethylated β-amino alcohols. Regiospecific ring-opening and rearrangement of the isolated, surprisingly stable aziridinium salts produces useful molecules including C-functionalized oxomorpholines and α,β-unsaturated amines. 2009 Wiley-VCH Verleg GmbH & Co. KGaA, Weinheim.

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