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Phenylcarbamic acid esters

Organic compounds that consist of a phenylcarbamic acid where the hydrogen atom bonded to the oxygen atom is replaced with an organic group; phenylcarbamic acid a carboxylic acid bonded to an amino group with a phenyl group substitution.
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Physical Form

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Boiling Point

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Search Within Results
Keyword Search:
736 – 750 of 1,673 results
736

eMolecules​ 501015-22-1 | Boc-(r)-3-amino-3-(4-cyano-phenyl)-propionic acid | Combi-Blocks | MFCD03427968 | 290.319 | C15H18N2O4 | 98.000 | CC(C)(C)OC(=O)N[C@H](CC(O)=O)c1ccc(cc1)C#N | 1g | 232332032

Boc-(r)-3-amino-3-(4-cyano-phenyl)-propionic acid | Combi-Blocks | 501015-22-1 | MFCD03427968 | 290.319 | C15H18N2O4 | 98.000 | CC(C)(C)OC(=O)N[C@H](CC(O)=O)c1ccc(cc1)C#N | 1g | 232332032

ENCOMPASS_PREFERRED
737

Aobchem AOBCHEM

5001086108 2- METHYLTHIO PHENYLBORONIC AC

ENCOMPASS_PREFERRED
738

Aobchem AOBCHEM

5001073435 N N-DIETHYLBENZENEPROPANAMIDE

ENCOMPASS_PREFERRED
739

GRAINGER INC N-LAURYLDIETHANOLAMINE 25G

502781175 N-LAURYLDIETHANOLAMINE 25G

ENCOMPASS_PREFERRED
740

eMolecules​ EMOLECULES INC

5000841237 N-BOC-4-IODOPIPERIDINE 25G

ENCOMPASS_PREFERRED
741

eMolecules​ 137076-22-3 | N-Boc-4-piperidinecarboxaldehyde | Oakwood Chemicals | MFCD02179019 | 213.277 | C11H19NO3 | 97.000 | CC(C)(C)OC(=O)N1CCC(CC1)C=O | 5g | 480128115

N-Boc-4-piperidinecarboxaldehyde | Oakwood Chemicals | 137076-22-3 | MFCD02179019 | 213.277 | C11H19NO3 | 97.000 | CC(C)(C)OC(=O)N1CCC(CC1)C=O | 5g | 480128115

ENCOMPASS_PREFERRED
742

Medchemexpress LLC (R)-1-Boc-3-methyl-piperazine | 163765-44-4 | 99.86% | 200.28 | 100 G
SDP

(R)-1-Boc-3-methyl-piperazine is a chemical intermediate. It can be used for the preparation of Compound I3.

  • Exhibits anticancer activity against colorectal adenocarcinoma with BRCA2 gene deletion.

ENCOMPASS_PREFERRED
743

eMolecules​ 98-80-6 | Phenylboronic acid | Chem-Impex | MFCD00002103 | 121.930 | C6H7BO2 | 99.000 | OB(O)c1ccccc1 | 100g | 112766136

Phenylboronic acid | Chem-Impex | 98-80-6 | MFCD00002103 | 121.930 | C6H7BO2 | 99.000 | OB(O)c1ccccc1 | 100g | 112766136

ENCOMPASS_PREFERRED
744

eMolecules​ 639091-78-4 | 2-(Boc-amino)-4-(aminomethyl)pyridine | Accela ChemBio (ASD) | MFCD06213871 | 223.276 | C11H17N3O2 | 95.000 | CC(C)(C)OC(=O)Nc1cc(CN)ccn1 | 0.25g | 512018508

2-(Boc-amino)-4-(aminomethyl)pyridine | Accela ChemBio (ASD) | 639091-78-4 | MFCD06213871 | 223.276 | C11H17N3O2 | 95.000 | CC(C)(C)OC(=O)Nc1cc(CN)ccn1 | 0.25g | 512018508

ENCOMPASS_PREFERRED
745

Bioss Unphosphorylated N-Cadherin Ty

Unphosphorylated N-Cadherin Tyr-820 Antibody

ENCOMPASS_PREFERRED
746

Medchemexpress LLC Acid-PEG3-C2-Boc | 1807539-06-5 | ≥97.0% | 100 MG
SDP

Acid-PEG3-C2-Boc is a PEG- and Alkyl/ether-based PROTAC linker. It can be used in the synthesis of PROTACs for the degradation of EGFR and inhibition of mTOR. PROTACs utilize the intracellular ubiquitin-proteasome system to selectively degrade target proteins.

  • Peg- and alkyl/ether-based protac linker
  • Can be used in the synthesis of protacs
  • Potential for degradation of egfr
  • Potential for inhibition of mtor

ENCOMPASS_PREFERRED
747

Aobchem AOBCHEM

5001088807 N-CYCLOHEXYLCYCLOHEXANECARBOXA

ENCOMPASS_PREFERRED
748

Medchemexpress LLC N-nitrosodicyclohexylamine | 947-92-2 | MFCD00021331 | 99.0% | 210.32 g/mol | C12H22N2O | 1 ML
SDP

N-Nitrosodicyclohexylamine (NDCHA) is provided as a 10 mM solution in dimethyl sulfoxide (DMSO) for research use. It is reported to have anti-androgenic activity and is supplied at high purity for in vitro pharmacology and biochemical studies.

  • 10 mM solution in DMSO.
  • Packaged as a 1 mL vial.
  • Purity ≥99.0%.
  • Molecular weight 210.32 g/mol.
  • For research use only; not for human use.

ENCOMPASS_PREFERRED
749

Aobchem AOBCHEM

5001092078 3- N-BOC-AMINOMETHYL PHENYLBOR

ENCOMPASS_PREFERRED
750

Medchemexpress LLC Bromo-PEG8-Boc | 1623792-00-6 | 99.9% | C23H45BrO10 | 100 MG
SDP

Bromo-PEG8-Boc is a PEG-based PROTAC linker designed for use in the synthesis of PROTACs. PROTACs function by leveraging the intracellular ubiquitin-proteasome system to selectively degrade target proteins.

  • Utilized in the synthesis of PROTACs.
  • Leverages the intracellular ubiquitin-proteasome system.
  • Facilitates selective degradation of target proteins.

ENCOMPASS_PREFERRED