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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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Boiling Point

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Search Within Results
Keyword Search:
1,171 – 1,185 of 1,673 results
1,171

eMolecules​ 270596-39-9 | Boc-(S)-3-amino-4-(3-chloro-phenyl)-butyric acid | Combi-Blocks, Inc. | MFCD01860999 | 313.780 | C15H20ClNO4 | 97.000 | CC(C)(C)OC(=O)N[C@H](CC(O)=O)Cc1cccc(Cl)c1 | 5g | 796999294

Boc-(S)-3-amino-4-(3-chloro-phenyl)-butyric acid | Combi-Blocks, Inc. | 270596-39-9 | MFCD01860999 | 313.780 | C15H20ClNO4 | 97.000 | CC(C)(C)OC(=O)N[C@H](CC(O)=O)Cc1cccc(Cl)c1 | 5g | 796999294

ENCOMPASS_PREFERRED
1,172

eMolecules​ 516-12-1 | N-Iodosuccinimide | ChemScene | MFCD00005512 | 224.985 | C4H4INO2 | 97.000 | IN1C(=O)CCC1=O | 10g | 665615973

N-Iodosuccinimide | ChemScene | 516-12-1 | MFCD00005512 | 224.985 | C4H4INO2 | 97.000 | IN1C(=O)CCC1=O | 10g | 665615973

ENCOMPASS_PREFERRED
1,173

eMolecules​ 288154-18-7 | 1-Boc-4-amino-4-(aminocarbonyl)piperidine | Acrotein ChemBio Inc. | MFCD04114477 | 243.307 | C11H21N3O3 | 97.000 | CC(C)(C)OC(=O)N1CCC(N)(CC1)C(N)=O | 25g | 625591641

1-Boc-4-amino-4-(aminocarbonyl)piperidine | Acrotein ChemBio Inc. | 288154-18-7 | MFCD04114477 | 243.307 | C11H21N3O3 | 97.000 | CC(C)(C)OC(=O)N1CCC(N)(CC1)C(N)=O | 25g | 625591641

ENCOMPASS_PREFERRED
1,174

eMolecules​ 288154-18-7 | 1-Boc-4-amino-4-(aminocarbonyl)piperidine | Acrotein ChemBio Inc. | MFCD04114477 | 243.307 | C11H21N3O3 | 97.000 | CC(C)(C)OC(=O)N1CCC(N)(CC1)C(N)=O | 5g | 625591640

1-Boc-4-amino-4-(aminocarbonyl)piperidine | Acrotein ChemBio Inc. | 288154-18-7 | MFCD04114477 | 243.307 | C11H21N3O3 | 97.000 | CC(C)(C)OC(=O)N1CCC(N)(CC1)C(N)=O | 5g | 625591640

ENCOMPASS_PREFERRED
1,175

eMolecules​ 114653-19-9 | (E)-3-(tert-Butyldimethylsilyloxy)propene-1-yl-boronic acid pinacol ester | Combi-Blocks, Inc. | MFCD15144803 | 298.310 | C15H31BO3Si | 97.000 | CC(C)(C)[Si](C)(C)OC\C=C\B1OC(C)(C)C(C)(C)O1 | 10g | 603198745

(E)-3-(tert-Butyldimethylsilyloxy)propene-1-yl-boronic acid pinacol ester | Combi-Blocks, Inc. | 114653-19-9 | MFCD15144803 | 298.310 | C15H31BO3Si | 97.000 | CC(C)(C)[Si](C)(C)OC\C=C\B1OC(C)(C)C(C)(C)O1 | 10g | 603198745

ENCOMPASS_PREFERRED
1,176

Medchemexpress LLC N-Benzyllinoleamide | 18286-71-0 | 1 ML
SDP

N-Benzyllinoleamide is a compound isolated from Lepidium meyenii Walp. It is known for its pharmaceutical properties that combat exercise-induced fatigue and is intended for research use only.

  • Isolated from Lepidium meyenii Walp.
  • Possesses anti-fatigue properties
  • Intended for research use only
  • Inhibits LPS-induced TNFalpha production in THP-1 cells (IC50: 14.2 μM)
  • Inhibits AEA uptake in U-937 cells (IC50: 0.67 μM)
  • Inhibits FAAH-mediated AEA hydrolysis in U-937 cells (IC50: 4.07 μM)
  • Molecular weight: 369.58
  • Formula: C25H39NO
  • Appearance: White to off-white solid
  • Soluble in DMSO (100 mg/mL)

ENCOMPASS_PREFERRED
1,177

Aobchem AOBCHEM

5000924716 5-CHLORO-3- METHTHIO PHENYLBOR

ENCOMPASS_PREFERRED
1,178

Medchemexpress LLC N-chlorosuccinimide | 128-09-6 | MFCD00005511 | 99.1% | 133.53 g/mol | C4H4ClNO2 | 1mL
SDP

N-Chlorosuccinimide is a five-membered N-containing heterocyclic molecule N-Chlorosuccinimide is a versatile reagent and can be used for different types of reactions such as aliphatic and aromatic chlorination N-Chlorosuccinimide can enhance the antimicrobial effect of Benzalkonium chloride (HY-B2232) on biofilm Pseudomonas aeruginosa[1][2]

ENCOMPASS_PREFERRED
1,179

Medchemexpress LLC Boc-C14-COOH | 843666-27-3 | 97.0% | 342.51 g·mol⁻¹ | C20H38O4 | 10 G
SDP

Boc-C14-COOH is a Boc-protected C14 alkyl carboxylic acid used as a non-cleavable linker in antibody-drug conjugate (ADC) synthesis and as an alkyl-chain linker for PROTAC design.

  • Non-cleavable ADC linker for conjugation chemistry.
  • Alkyl-chain PROTAC linker for targeted protein degradation.
  • Molecular formula C20H38O4, molecular weight 342.51 g·mol⁻¹.
  • Purity typically 97.0% as supplied.
  • Available in laboratory pack sizes, including 10 G.

ENCOMPASS_PREFERRED
1,180

Medchemexpress LLC N-Boc-nortropinone | 185099-67-6 | 225.29 | 25 G
SDP

N-Boc-nortropinone is a biochemical reagent intended for life science related research. It is an organic compound that contains a Boc group, which can be deprotected under mild acidic conditions to yield a free amine. This makes it applicable to research involving the synthesis of peptide compounds.

  • Biochemical reagent for life science research
  • Contains a Boc group for deprotection
  • Suitable for synthesis of peptide compounds
  • For research use only

ENCOMPASS_PREFERRED
1,181

Medchemexpress LLC Acid-PEG3-C2-Boc | 1807539-06-5 | ≥97.0% | 50 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 consist of two different ligands connected by a linker; one ligand is for an E3 ubiquitin ligase and the other is for the target protein. PROTACs function by utilizing the intracellular ubiquitin-proteasome system to selectively degrade target proteins.

  • Peg- and alkyl/ether-based PROTAC linker
  • Used in the synthesis of PROTACs for the degradation of EGFR
  • Used in the synthesis of PROTACs for the inhibition of mTOR
  • Utilizes the intracellular ubiquitin-proteasome system to selectively degrade target proteins

ENCOMPASS_PREFERRED
1,182

eMolecules​ 516-12-1 | N-Iodosuccinimide | AA Blocks LLC | MFCD00005512 | 224.985 | C4H4INO2 | 0.000 | IN1C(=O)CCC1=O | 10g | 784389342

N-Iodosuccinimide | AA Blocks LLC | 516-12-1 | MFCD00005512 | 224.985 | C4H4INO2 | 0.000 | IN1C(=O)CCC1=O | 10g | 784389342

ENCOMPASS_PREFERRED
1,183

eMolecules​ 98-80-6 | Phenylboronic acid | Ambeed | MFCD00002103 | 121.930 | C6H7BO2 | 98.000 | OB(O)c1ccccc1 | 1000g | 490494397

Phenylboronic acid | Ambeed | 98-80-6 | MFCD00002103 | 121.930 | C6H7BO2 | 98.000 | OB(O)c1ccccc1 | 1000g | 490494397

ENCOMPASS_PREFERRED
1,184

Medchemexpress LLC SULT1A3 Human N-Hi 50ug
SDP

Recombinant human SULT1A3 protein with an N-terminal 6xHis tag, expressed in Escherichia coli and supplied lyophilized for biochemical and enzymatic studies. The enzyme catalyzes PAPS-dependent sulfate conjugation of phenolic monoamines (for example dopamine, norepinephrine, and serotonin) and is provided with high purity and a stabilized formulation for storage and handling.

  • Recombinant human sequence, full-length isoform 1.
  • N-terminal 6xHis tag for affinity purification and detection.
  • Expressed in E. coli for efficient production.
  • Lyophilized formulation for improved shelf stability.
  • Formulated in PBS with trehalose, mannitol, and Tween 80 for protection during storage.
  • Purity greater than 95% as determined by reducing SDS-PAGE.
  • Supplied in microgram quantities suitable for biochemical assays.
  • Recommended storage at -20 °C to -80 °C; aliquot after reconstitution.

ENCOMPASS_PREFERRED
1,185

eMolecules​ 843666-40-0 | Boc-C16-COOH | ChemScene | MFCD09991735 | 370.574 | C22H42O4 | 97.000 | CC(C)(C)OC(=O)CCCCCCCCCCCCCCCCC(O)=O | 5g | 572174034

Boc-C16-COOH | ChemScene | 843666-40-0 | MFCD09991735 | 370.574 | C22H42O4 | 97.000 | CC(C)(C)OC(=O)CCCCCCCCCCCCCCCCC(O)=O | 5g | 572174034

ENCOMPASS_PREFERRED