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2-((S)-2-tert-Butoxycarbonylamino-propionylamino)-benzoic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119422-40-1

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119422-40-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119422-40-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,4,2 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 119422-40:
(8*1)+(7*1)+(6*9)+(5*4)+(4*2)+(3*2)+(2*4)+(1*0)=111
111 % 10 = 1
So 119422-40-1 is a valid CAS Registry Number.

119422-40-1Relevant academic research and scientific papers

Efficient synthesis of biologically important chiral 2-alkylamino benzoxazinones

Mohapatra, Debendra K.,Datta, Apurba

, p. 2527 - 2530 (1997)

A novel general method has been developed for the synthesis of various amino acid derived chiral 2-substituted benzoxazinones, known inhibitors of standard serine proteases of the chymotrypsin superfamily.

First total synthesis of versicotide A, B and C

Posada, Laura,Davyt, Danilo,Serra, Gloria

, p. 43653 - 43659 (2020)

The syntheses of versicotides A-C, natural products containing anthranilic acid and NMe-Ala, were achieved by solid phase peptide synthesis on 2-chlorotrityl resin followed by solution phase macrocyclization. Using an oxyma additive, the difficult coupling reactions to the deactivated aromatic amine of o-aminobenzoic acid, were performed in high yield, avoiding anthranilic rearrangements or side reactions. This journal is

Synthesis and anticancer activity of conformationally constrained Smac mimetics containing pseudo β turns

Baravkar, Sachin B.,Wagh, Mahendra A.,Paul, Debasish,Santra, Manas,Sanjayan, Gangadhar J.

supporting information, p. 3473 - 3476 (2018/08/24)

Herein, we report synthesis and in vitro anticancer activity of conformationally constrained Smac mimetics containing reverse turn inducing motifs “Ant-Pro” and “sAnt-Pro”. The synthesis of Smac analogs with diverse hydrophobic groups at the C-

New routes to 1,4-benzodiazepin-2,5-diones

Akssira,Boumzebra,Kasmi,Dahdouh,Roumestant,Viallefont

, p. 9051 - 9060 (2007/10/02)

1,4-benzodiazepin-2,5-diones have been synthesized in good overall yields by two routes, the first one by cyclisation of dipeptides prepared from Boc anthranilic acid and α-amino acid methyl esters, the second one by reaction of N-carboxy α-amino acid anhydrides with Boc anthranilic acid.

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