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Carbamic acid, (1-cyano-2-phenylethyl)-, 9H-fluoren-9-ylmethyl ester, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

193086-69-0

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193086-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 193086-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,0,8 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 193086-69:
(8*1)+(7*9)+(6*3)+(5*0)+(4*8)+(3*6)+(2*6)+(1*9)=160
160 % 10 = 0
So 193086-69-0 is a valid CAS Registry Number.

193086-69-0Downstream Products

193086-69-0Relevant academic research and scientific papers

A simple preparation of N-protected chiral α-aminonitriles from N-protected α-amino acid amides

Maetz, Philippe,Rodriguez, Marc

, p. 4221 - 4222 (1997)

N-protected α-amino-acid amides are dehydrated to N-protected α-aminonitriles in good yields and with excellent purities by reaction of the corresponding primary amides with cyanuric chloride in DMF.

Dehydration of Chiral α-Amides to Chiral α-Nitriles Under the Appel Reaction Conditions

Shekharappa,Roopesh Kumar,Srinivasulu,Sureshbabu, Vommina V.

, p. 497 - 502 (2020/07/30)

An efficient synthesis of Nα-protected amino nitriles from Nα-protected amino acid amides employing Ph3P, I2 and NMM was described. Various amino acid amides, protected by Fmoc, Z and Boc were conveniently conve

One-pot synthesis of orthogonally protected dipeptide selenazoles employing Nα-amino selenocarboxamides and α-bromomethyl ketones

Madhu, Chilakapati,Panguluri, Nageswara Rao,Narendra,Panduranga,Sureshbabu, Vommina V.

, p. 6831 - 6835 (2015/01/09)

A simple and efficient protocol for the synthesis of selenazole containing dipeptidomimetics using Nα-amino selenocarboxamides and α-bromomethyl ketones is described. All the compounds made were isolated in good yields and fully characterized.

A novel approach to the solid-phase synthesis of peptides with a tetrazole at the C-terminus

Gunn, Sarah J.,Baker, Alison,Bertram, Richard D.,Warriner, Stuart L.

, p. 2643 - 2646 (2008/02/12)

Peptidomimetics containing a C-terminal tetrazole can be easily prepared using modifications to traditional peptide synthesis protocols. Georg Thieme Verlag Stuttgart.

Syntheses of Fmoc-α-aminoalkyltetrazoles and tetrazole analogue of Leu-enkephalin

Manturewicz,Kosson,Grzonka

, p. 1327 - 1334 (2008/09/18)

Five Fmoc-α-aminoalkyltetrazoles were synthesized starting from Fmoc-α-amino acids. Fmoc-LeuT was applied in synthesis of tetrazole analogue of Leu-enkephalin by solid phase peptide synthesis (SPPS), as well as in solution. Radioreceptor assays showed hig

Synthesis of tetrazole analogues of amino acids using Fmoc chemistry: isolation of amino free tetrazoles and their incorporation into peptides

Sureshbabu, Vommina V.,Venkataramanarao, Rao,Naik, Shankar A.,Chennakrishnareddy

, p. 7038 - 7041 (2008/03/12)

An efficient synthesis of tetrazole analogues of amino acids starting from Nα-Fmoc amino acid in a three-step protocol is reported. The free amino tetrazoles were obtained in good yields and with excellent purity after removal of the Fmoc group

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