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(S)-2-(((cyclohexyloxy)carbonyl)amino)-3-methylbutanoic acid is a complex organic compound with the molecular formula C14H23NO4. It is a chiral molecule, with the "S" indicating that it is the (S)-enantiomer, which means it has a specific three-dimensional arrangement of atoms. (S)-2-(((cyclohexyloxy)carbonyl)amino)-3-methylbutanoic acid features a cyclohexyloxycarbonyl group, which is a cyclic structure attached to a carbonyl group, and an amino group connected to a 3-methylbutanoic acid moiety. The molecule is characterized by its unique arrangement of functional groups, which can influence its reactivity and potential applications in various chemical or pharmaceutical contexts.

3514-03-2

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3514-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3514-03-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,1 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3514-03:
(6*3)+(5*5)+(4*1)+(3*4)+(2*0)+(1*3)=62
62 % 10 = 2
So 3514-03-2 is a valid CAS Registry Number.

3514-03-2Downstream Products

3514-03-2Relevant academic research and scientific papers

NOVEL HEPATITIS C VIRUS INHIBITORS

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Page/Page column 63; 65, (2013/07/05)

The invention provides compounds of formula (I): wherein Rings A and A' are independently 5-membered optionally substituted aromatic heterocycles; Q is C(=O)NR1R1' or formula U is C(R4)2, O, S, S(=O)2, C(R4)2C(R4)2, CH2O, OCH2, CH2S, SCH2, CH2S(=O)2, S(=O)CH2 or C=C(Ru )2; X is CH2, CHR12, CR12R12, O, S, S(=O)2 or NRx; m is 0, 1, 2 or 3; n is 0, 1, 2 or 3; the other variables are as defined in the claims, which are of use in the treatment or prophylaxis of hepatitis C virus infection, and related aspects.

Cyclohexyloxycarbonyl based orthogonal solid phase peptide synthesis in Boc chemistry

Mezo, Gabor,Mihala, Nikolett,Koczan, Gyoergy,Hudecz, Ferenc

, p. 6757 - 6766 (2007/10/03)

Application of N-cyclohexyloxocarbonyl (Choc) protection in Boc chemistry on solid phase provides a new possibility for the preparation of protected peptide fragments. A Choc/OcHex protection scheme allows also the assembly of cyclic lactam peptides linked to the resin through the C- terminus. Choc protection is stable under the 1M TMSOTf-thioanisole/TFA cleavage condition at 0°C, but it is removable by anhydrous HF. We have utilized cyclohexyloxycarbonyl as an orthogonal protecting group for the synthesis of a i) bicyclic epitope peptide of glycoprotein D of HSV 1 on BHA resin and ii) fully protected hexapeptide involved in protein transport on Merrifield resin.

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