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Filtered Search Results
eMolecules 78767-55-2 | Benzyl 4-formylbenzoate | Combi-Blocks, Inc. | MFCD00447122 | 240.258 | C15H12O3 | 98.000 | O=Cc1ccc(cc1)C(=O)OCc1ccccc1 | 5g | 808883312
Benzyl 4-formylbenzoate | Combi-Blocks, Inc. | 78767-55-2 | MFCD00447122 | 240.258 | C15H12O3 | 98.000 | O=Cc1ccc(cc1)C(=O)OCc1ccccc1 | 5g | 808883312
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eMolecules 83948-53-2 | tert-butyl N-(3-bromopropyl)carbamate | Pharmablock | MFCD02683429 | 238.125 | C8H16BrNO2 | 97.000 | CC(C)(C)OC(=O)NCCCBr | 10g | 594229723
tert-butyl N-(3-bromopropyl)carbamate | Pharmablock | 83948-53-2 | MFCD02683429 | 238.125 | C8H16BrNO2 | 97.000 | CC(C)(C)OC(=O)NCCCBr | 10g | 594229723
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eMolecules 81927-55-1 | Benzyl-2,2,2-trichloroacetamide | Ambeed | MFCD00000805 | 252.520 | C9H8Cl3NO | 98.000 | ClC(Cl)(Cl)C(=N)OCc1ccccc1 | 100g | 490502485
Benzyl-2,2,2-trichloroacetamide | Ambeed | 81927-55-1 | MFCD00000805 | 252.520 | C9H8Cl3NO | 98.000 | ClC(Cl)(Cl)C(=N)OCc1ccccc1 | 100g | 490502485
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eMolecules 81927-55-1 | Benzyl-2,2,2-trichloroacetamide | Ambeed | MFCD00000805 | 252.520 | C9H8Cl3NO | 98.000 | ClC(Cl)(Cl)C(=N)OCc1ccccc1 | 25g | 490502484
Benzyl-2,2,2-trichloroacetamide | Ambeed | 81927-55-1 | MFCD00000805 | 252.520 | C9H8Cl3NO | 98.000 | ClC(Cl)(Cl)C(=N)OCc1ccccc1 | 25g | 490502484
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eMolecules 53844-02-3 | Benzyl (2-bromoethyl)carbamate | Synthonix - Stock | MFCD09909490 | 258.115 | C10H12BrNO2 | 95.000 | BrCCNC(=O)OCc1ccccc1 | 25g | 448042478
Benzyl (2-bromoethyl)carbamate | Synthonix - Stock | 53844-02-3 | MFCD09909490 | 258.115 | C10H12BrNO2 | 95.000 | BrCCNC(=O)OCc1ccccc1 | 25g | 448042478
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Medchemexpress LLC L-Glutamate-γ-benzyl ester | 1676-73-9 | 99.88% | 237.25 | 100 G
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L-Glutamate-γ-benzyl ester is a glutamic acid derivative. Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances.
- Glutamic acid derivative
- For research use only
- Influences anabolic hormone secretion
- Supplies fuel during exercise
- Enhances mental performance during stress
- Prevents exercise-induced muscle damage
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eMolecules 30379-58-9 | Benzyl 2-Hydroxyacetate | Accela ChemBio (ASD) | MFCD00191776 | 166.176 | C9H10O3 | 95.000 | OCC(=O)OCc1ccccc1 | 5g | 527373443
Benzyl 2-Hydroxyacetate | Accela ChemBio (ASD) | 30379-58-9 | MFCD00191776 | 166.176 | C9H10O3 | 95.000 | OCC(=O)OCc1ccccc1 | 5g | 527373443
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eMolecules 1857523-19-3 | Benzyl 2-Methylazepane-1-Carboxylate | 250mg
Medchem Express | Avosentan | 5mg | 446265140 | HY-15195 | 290815-26-8 | MFCD23843806 | 479.510 | C23H21N5O5S
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Medchemexpress LLC (R)-2-(((Benzyloxy)carbonyl)amino)-3,3-dimethylbutanoic acid | 70874-05-4 | 96.2% | C₁₄H₁₉NO₄ | 100 MG
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This chemical compound is a leucine derivative, identified by CAS number 70874-05-4. It has a molecular formula of C₁₄H₁₉NO₄ and a molecular weight of 265.30, appearing as a colorless to light yellow liquid with an HPLC purity of 96.17%.
- High purity of 96.17% as determined by HPLC
- Identified as a leucine derivative
- Molecular formula C₁₄H₁₉NO₄
- Molecular weight 265.30
- Appears as a colorless to light yellow liquid
- Defined storage guidelines for pure form and in solvent
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![Medchemexpress LLC 7-Benzyl-2,7-diazaspiro[3.5]nonane dihydrochloride | 1334536-89-8 | 95% | 289.24 | 5 G](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000401221-logo.png-250.jpg){kind=logo}
Medchemexpress LLC 7-Benzyl-2,7-diazaspiro[3.5]nonane dihydrochloride | 1334536-89-8 | 95% | 289.24 | 5 G
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7-Benzyl-2,7-diazaspiro[3.5]nonane dihydrochloride is a drug intermediate for synthesis of various active compounds.
- Molecular formula: C14H22Cl2N2
- Target: Drug intermediate
- Pathway: Others
- Powder storage: -20°C for 3 years, 4°C for 2 years
- In solvent storage: -80°C for 6 months, -20°C for 1 month
- Application: Reference compound
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eMolecules 6063-50-9 | N-Benzyl-2,2-dichloroacetamide | Toronto Research Chemicals | MFCD01124802 | 218.080 | C9H9Cl2NOClC(Cl)C(=O)NCc1ccccc1 | 50mg | 601590039
N-Benzyl-2,2-dichloroacetamide | Toronto Research Chemicals | 6063-50-9 | MFCD01124802 | 218.080 | C9H9Cl2NOClC(Cl)C(=O)NCc1ccccc1 | 50mg | 601590039
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eMolecules 80171-34-2 | 1-Bromo-2-(ethoxymethyl)benzene | Combi-Blocks | MFCD09972176 | 215.090 | C9H11BrO | 97.000 | CCOCc1ccccc1Br | 1g | 117542448
1-Bromo-2-(ethoxymethyl)benzene | Combi-Blocks | 80171-34-2 | MFCD09972176 | 215.090 | C9H11BrO | 97.000 | CCOCc1ccccc1Br | 1g | 117542448
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Cayman Chemical R-TrItyl glycIdyl ether 5g
A synthetic precursor; has been used in the synthesis of glycerophospholipids, as well as compounds with antiviral and antimalarial activities
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Medchemexpress LLC BAY-707 | 2109805-96-9 | 99.6% | 288.34 | 10 MG
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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BAY-707 is a chemical probe that functions as a substrate-competitive, highly potent, and selective inhibitor of MTH1(NUDT1) with an IC50 of 2.3 nM. It exhibits a favorable pharmacokinetic profile compared to other MTH1 compounds and is well-tolerated in mice, though it does not demonstrate in vitro or in vivo anticancer efficacy.
- Substrate-competitive inhibitor of MTH1(NUDT1).
- Highly potent and selective (IC50 of 2.3 nM).
- Good pharmacokinetic profile.
- Well-tolerated in mice.
- Superior cellular target engagement (EC50 of 7.6 nM).
- High cell permeability (Caco-2 assay).
- Favorable physicochemical profile.
- Promising in vitro pharmacokinetic properties.
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Sigma Aldrich Fine Chemicals Biosciences (R)-(−)-α-Methoxy-α-(trifluoromethyl)phenylacetyl chloride, 39637-99-5, MFCD00044400, 500 mg
Linear Formula: C6H5C(OCH3)(CF3)COCl, Molecular Weight: 252.62, for chiral derivatization, LiChropur, ≥99.0%, Synonym: (R)-(−)-MTPA-Cl, Mosher’s acid chloride. It was used for derivatizing D-arabinitol and L-arabinitol samples for high performance thin layer chromatography (HPTLC) analysis for studying resolution of the diastereoisomer. Ready-to-use reagent for the determination of the enantiomeric purity of alcohols and amines after derivatization.
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