Reagent M

Reagent M contains an amino acid-derived scaffold presented as a reagent rather than an unmodified free amino acid, and it is supplied for chemical use in peptide- and amino-acid-related workflows. The molecule bears amino and carboxyl functionalities in a form consistent with derivatization or salt/protected-state handling, providing controlled chemoselectivity and compatibility with stepwise coupling or analytical derivatization depending on the exact reagent design. In biochemical supplier applications, Reagent M is typically employed as an intermediate or functionalized amino-acid reagent to enable synthesis of more complex amino acid and peptide derivatives, including labeled, conjugatable, or structurally modified targets.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

CAT No: CP26083

CAS No:87242-92-0

Synonyms/Alias:87242-92-0;[1-(4-METHOXY-BENZYLSULFANYL)-CYCLOHEXYL]-ACETICACID;ReagentM;AmbotzRL-2006;C16H22O3S;CTK8G2914;MolPort-008-268-974;ZINC2526318;KM2497;OR030752;V8415;3B3-062523;2-(1-{[(4-methoxyphenyl)methyl]sulfanyl}cyclohexyl)aceticacid;(1-{[(4-METHOXYPHENYL)METHYL]SULFANYL}CYCLOHEXYL)ACETICACID;beta-(4-Methoxy-benzylsulfanyl)-beta,beta-cyclopentamethylene-propionicacid,S-(4-Methoxybenzyl)-beta-mercapto-beta,beta-cyclopentamethylene-propionicacid

Chemical Name:2-(1-(4-Methoxybenzylthio)cyclohexyl)acetic acid

Custom Peptide Synthesis
cGMP Peptide
  • Registration of APIs
  • CMC information required for an IND
  • IND and NDA support
  • Drug master files (DMF) filing
M.F/Formula
C16H22O3S
M.W/Mr.
294,42 g/mole
Size
1 g;5 g;
InChI
1S/C16H22O3S/c1-19-14-7-5-13(6-8-14)12-20-16(11-15(17)18)9-3-2-4-10-16/h5-8H,2-4,9-12H2,1H3,(H,17,18)
InChI Key
BGXNGARHYXNGPK-UHFFFAOYSA-N
Canonical SMILES
COC1=CC=C(C=C1)CSC2(CCCCC2)CC(=O)O

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