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N-(8-methoxy-2-oxo-2H-chromen-3-yl)benzamide is a complex organic compound with the molecular formula C17H13NO4. It is a derivative of benzamide, featuring a chromen-3-yl group at the nitrogen atom. This molecule is characterized by a benzene ring attached to a chromene-2-one moiety, which includes an 8-methoxy substituent. The chromene-2-one ring is a heterocyclic compound with a benzene ring fused to a pyran ring, and the 2-oxo group indicates the presence of a carbonyl group at the 2-position. N-(8-methoxy-2-oxo-2H-chromen-3-yl)benzamide is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or materials science due to its unique structure and properties.

7150-00-7

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7150-00-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7150-00-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,5 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7150-00:
(6*7)+(5*1)+(4*5)+(3*0)+(2*0)+(1*0)=67
67 % 10 = 7
So 7150-00-7 is a valid CAS Registry Number.

7150-00-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(8-methoxy-2-oxo-2H-chromen-3-yl)benzamide

1.2 Other means of identification

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Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

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More Details:7150-00-7 SDS

7150-00-7Downstream Products

7150-00-7Relevant academic research and scientific papers

Rhodium-Catalyzed Asymmetric Hydrogenation of 3-Benzoylaminocoumarins for the Synthesis of Chiral 3-Amino Dihydrocoumarins

Xu, Yunnan,Liu, Delong,Deng, Yu,Zhou, Yi,Zhang, Wanbin

supporting information, p. 23602 - 23607 (2021/10/05)

An asymmetric hydrogenation of 3-benzoylaminocoumarins was achieved for the first time using our BridgePhos-Rh catalytic system, providing chiral 3-amino dihydrocoumarins in high yields (up to 98 %) and with excellent enantioselectivities (up to 99.7 % ee). The relationship between the enantioselectivities of the hydrogenations and the dihedral angles and the resulting π-π stacking effects of the BridgePhos-Rh complexes, which were determined by X-ray diffraction analysis, are discussed. The corresponding hydrogenated products allow for many transformations, providing several chiral skeletons with important physiological and pharmacological activities.

A one-pot [Bmim]OH-mediated synthesis of 3-benzamidocoumarins

Yadav, Lal Dhar S.,Singh, Santosh,Rai, Vijai K.

experimental part, p. 2208 - 2212 (2009/08/07)

The first example of an ionic liquid-promoted one-pot synthesis of 3-benzamidocoumarins from salicylaldehydes and 2-pheny-1,3-oxazolan-5-one via Knoevenagel condensation-ring transformation cascades has been reported. No by-product formation, operational

An efficient and facile synthesis of substituted 3-aminocoumarins under mw irradiation in dry media

Valizadeh, Hassan,Shockravi, Abbas

, p. 475 - 478 (2007/10/03)

A variety of 3-aminocoumarins were prepared by reaction of salicylaldehyde derivatives with benzoylglycine catalyzed by piperidine under microwave irradiation (MWI) and subsequent acid hydrolysis. The structure of products was proven by elemental analysis, IR, NMR and Mass spectra. These investigations will contribute to development of environmentally friendly and inexpensive processes in organic synthesis.

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