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Benzamide
Benzamide
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name Benzamide
Price:
CAS No.: 55-21-0
Catalog No.: CFN98925
Molecular Formula: C7H7NO
Molecular Weight: 121.1 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The herbs of Berberis pruinosa
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF
Similar structural: Comparison (Web)  (SDF)
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Size /Price /Stock 10 mM * 1 mL in DMSO / Inquiry
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Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries
Biological Activity
Description: Reference standards.
Benzamide Description
Source: The herbs of Berberis pruinosa
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 8.2576 mL 41.2882 mL 82.5764 mL 165.1528 mL 206.441 mL
5 mM 1.6515 mL 8.2576 mL 16.5153 mL 33.0306 mL 41.2882 mL
10 mM 0.8258 mL 4.1288 mL 8.2576 mL 16.5153 mL 20.6441 mL
50 mM 0.1652 mL 0.8258 mL 1.6515 mL 3.3031 mL 4.1288 mL
100 mM 0.0826 mL 0.4129 mL 0.8258 mL 1.6515 mL 2.0644 mL
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Protocol
Structure Identification:
Inorg Chem. 2015 Apr 20;54(8):3958-69.
Density functional theory study of Rh(III)-catalyzed C-H activations and intermolecular annulations between benzamide derivatives and allenes.[Pubmed: 25856513]

METHODS AND RESULTS:
Density functional theory has been applied to gain insight into the Cp*Rh(OAc)2-catalyzed C-H activation and intermolecular annulation of Benzamide derivatives with allenes. The study shows that the reactions proceed in three steps: (1) C-H activation induced by Rh catalyst reacting with Benzamide derivatives, (2) carborhodation of allene, and (3) regeneration of Rh catalyst. The results indicate that the N-H deprotonation makes the following C-H activation much easier. The regio- and stereoselectivities of 1a (N-pivaloyloxy Benzamide)/2a (cyclohexylallene) and 1b (N-pivaloyloxy-4-methyl-Benzamide)/2b (1,1-dimethyl allene) depend on the allene carborhodation step. The steric hindrance effect is the dominant factor. We also discuss the reaction mechanism of 1c (N-methoxy Benzamide)/2a.
CONCLUSIONS:
The chemoselectivity between 1c/2a is determined by the N-O cleavage step. Replacement of OPiv by OMe leads to loss of the stabilization effect provided by C=O in OPiv. Additionally, Cp*Rh(OAc)(OPiv) is produced in the Cp*Rh(OAc)2 regeneration step, which can work as catalyst as well.
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CAS No: 580-72-3
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Isosilybin

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CAS No: 72581-71-6
Price: $138/20mg
Berberine hydrochloride

Catalog No: CFN99562
CAS No: 633-65-8
Price: $30/20mg
Ginsenoside Rg1

Catalog No: CFN99967
CAS No: 22427-39-0
Price: $40/20mg
Honokiol

Catalog No: CFN99902
CAS No: 35354-74-6
Price: $30/20mg
Kaempferol-3-O-(2',6'-di-O-trans-p...

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CAS No: 121651-61-4
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3-oxo-Olean-12-en-28-oic acid

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5'-Guanylic acid

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Ginkgolide A

Catalog No: CFN99638
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Price: $40/20mg
Cucurbitacin A

Catalog No: CFN90324
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