65854-72-0
65854-72-0
Chemical Structure
2-Amino-5-Chlorobenzophenone-d5
- CAS No.: 65854-72-0
- Formula:C13H5D5ClNO
- Molecular Weight:236.71
IUPAC Name: (2-amino-5-chlorophenyl)(phenyl-d5)methanone
InChIKey: ZUWXHHBROGLWNH-RALIUCGRSA-N
SMILES: O=C(C1=C([2H])C([2H])=C([2H])C([2H])=C1[2H])C2=C(C=CC(Cl)=C2)N
Biological Activity: 2-Amino-5-Chlorobenzophenone-d5 is the deuterium labeled 2-Amino-5-Chlorobenzophenone[1].
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2-Amino-5-Chlorobenzophenone-d5 | 2-Amino-5-Chlorobenzophenone-d5 is the deuterium labeled 2-Amino-5-Chlorobenzophenone. | |||||||||||||||||||||
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2-Amino-5-chlorobenzophenone (Standard) | ≥98% | 2-Amino-5-chlorobenzophenone (Standard) is the analytical standard of 2-Amino-5-chlorobenzophenone. This product is intended for research and analytical applications. 2-Amino-5-chlorobenzophenone is a substituted benzophenone and can be used in the synthesis of benzodiazepines. The 2-Amino-5-chlorobenzophenone derivative has skeletal muscle relaxation activity. | ||||||||||||||||||||
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2-Amino-5-chlorobenzophenone | 99.98% | 2-Amino-5-chlorobenzophenone (5-Chloro-2-aminobenzophenone) is a chemical intermediate. Derivatives of 2-Amino-5-chlorobenzophenone serve as skeletal muscle relaxants. 2-Amino-5-chlorobenzophenone acts as a starting material for the synthesis of anti-biofilm 2-amino-5-chlorobenzophenone Schiff bases. 2-Amino-5-chlorobenzophenone is applicable to research related to bacterial infections.\n |
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G256 | G256 is a cytochrome P450 substrate with antiarrhythmic properties. In recombinant monooxygenase systems, G256 undergoes N-hydroxylation of the terminal aminoguanidine nitrogen, as well as ring hydroxylation catalyzed by cytochrome P4502C3. G256 generates N-hydroxyaminoguanidine metabolites via N-hydroxylation in liver microsomal fractions. G256 produces phenol metabolites through ring hydroxylation in both liver microsomal fractions and recombinant cytochrome P450 systems. G256 can be used for research on arrhythmias. | |||||||||||||||||||||
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2-Amino-5-nitrobenzophenone | 98.43% | 2-Amino-5-nitrobenzophenone (Ro-7-19990) is a degradation of benzodiazepines. 2-Amino-5-nitrobenzophenone can be used for research and forensic applications. | ||||||||||||||||||||
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2-Amino-5-chloro-2'-fluorobenzophenone | 2-Amino-5-chloro-2'-fluorobenzophenone is a precursor in the synthesis of Midazolam. | |||||||||||||||||||||
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2-Amino-2',5-dichlorobenzophenone | 99.95% | (2-Amino-5-chlorophenyl)(2-chlorophenyl)methanone is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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2,4'-Dichlorobenzophenone | 98.52% | 2,4'-Dichlorobenzophenone is a dichlorinated benzophenone and intermediate in the synthesis of selected fungicides and other agricultural products. | ||||||||||||||||||||
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5-Chloro-2-(methylamino)benzophenone | 99.21% | (5-Chloro-2-(methylamino)phenyl)(phenyl)methanone is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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2,4-Dihydroxybenzophenone-13C6 | 2,4-Dihydroxybenzophenone-13C6 (Ultraviolet absorber UV-0-13C6) is the 13C- and deuterium labeled (2,4-Dihydroxyphenyl)(phenyl)methanone. | |||||||||||||||||||||
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2-Amino-5-bromobenzophenone | 99.82% | 2-Amino-5-bromobenzophenone (2-Benzoyl-4-bromoaniline) is a derivative of benzophenone (HY-Y0546) that can be used in the synthesis of pharmaceutical compounds. | ||||||||||||||||||||
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2-Amino-5-bromo-2’-chlorobenzophenone | 98.81% | 2-Amino-5-bromo-2’-chlorobenzophenone is a precursor in the synthesis of Phenazepam.1 2-Amino-5-bromo-2’-chlorobenzophenone is also an active metabolite of Phenazepam. | ||||||||||||||||||||
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Nordiazepam uncyclized intermediate hydrochloride | 99.32% | Nordiazepam uncyclized intermediate hydrochloride is a prodrug form of Nordiazepam. | ||||||||||||||||||||
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