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N-[(4-Bromophenyl)(phenyl)methyl]acetamide is a chemical compound with the molecular formula C15H14BrNO. It is a derivative of acetamide, featuring a 4-bromophenyl group and a phenyl group attached to the methylene bridge. N-[(4-BroMophenyl)(phenyl)Methyl]acetaMide is characterized by its aromatic structure and bromine atom, which can participate in various chemical reactions, such as substitution or addition reactions. It has potential applications in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structure and reactivity.

5580-51-8

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5580-51-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5580-51-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,8 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5580-51:
(6*5)+(5*5)+(4*8)+(3*0)+(2*5)+(1*1)=98
98 % 10 = 8
So 5580-51-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H13NO4S/c1-3-18-9-5-4-8(6-10(9)17-2)7-11-12(15)14-13(16)19-11/h4-7H,3H2,1-2H3,(H,14,15,16)/b11-7-

5580-51-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(4-bromophenyl)-phenylmethyl]acetamide

1.2 Other means of identification

Product number -
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

1.5 Emergency phone number

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More Details:5580-51-8 SDS

5580-51-8Downstream Products

5580-51-8Relevant academic research and scientific papers

Bis-sulfamyl imines: Potent substrates for asymmetric additions of arylboroxines under rhodium catalysis

Crampton, Rosemary,Woodward, Simon,Fox, Martin

supporting information; experimental part, p. 903 - 906 (2011/06/19)

Bis-sulfamyl imines are shown to be potentially ideal substrates for rhodium-catalysed asymmetric additions of arylboron nucleophiles as they show: (i) near perfect enantioselectivities (11 examples, 98-99+% ee), (ii) good to excellent diastereoselectivities (10-32:1 rac:meso), and (iii) high functional group tolerance in removal of the low molecular weight protecting group via mild heating in aqueous pyridine.

The ritter reaction under truly catalytic bronsted acid conditions

Sanz, Roberto,Martinez, Alberto,Guilarte, Veronica,Alvarez-Gutierrez, Julia M.,Rodriguez, Felix

, p. 4642 - 4645 (2008/03/12)

Simple organic acids like 2,4-dinitrobenzenesulfonic acid (DNBSA) catalyze the Ritter reaction of secondary benzylic alcohols giving rise to the corresponding N-benzylacetamides in usually high yields. Reactions can be conducted without exclusion of oxygen and without the need of dry solvents. With tertiary α,α-dimethylbenzylic alcohols a different pathway involving a formal dimerization reaction takes place under the acid-catalytic conditions used. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.

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