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3-(4-bromophenyl)propionamide is a chemical compound with the molecular formula C9H10BrNO. It is a derivative of propionamide, featuring a 4-bromophenyl group attached to the third carbon of the propionamide chain. 3-(4-bromophenyl)propionamide is characterized by its amide functional group, which consists of a carbonyl group (C=O) and a nitrogen atom (N) with a single hydrogen atom and an alkyl group attached. The presence of the bromine atom in the 4-position of the phenyl ring introduces a significant change in the compound's physical and chemical properties, such as increased molecular weight, altered reactivity, and potential applications in various chemical reactions. 3-(4-bromophenyl)propionamide is often used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals due to its versatile structure and reactivity.

57775-11-8

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57775-11-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57775-11-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,7,7 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 57775-11:
(7*5)+(6*7)+(5*7)+(4*7)+(3*5)+(2*1)+(1*1)=158
158 % 10 = 8
So 57775-11-8 is a valid CAS Registry Number.

57775-11-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-bromophenyl) propanamide

1.2 Other means of identification

Product number -
Other names 42759 3-(4-BROMOPHENYL)PROPANAMIDE

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:57775-11-8 SDS

57775-11-8Relevant academic research and scientific papers

Visible-Light Decatungstate/Disulfide Dual Catalysis for the Hydro-Functionalization of Styrenes

Prieto, Alexis,Taillefer, Marc

supporting information, p. 1484 - 1488 (2021/03/08)

We describe an efficient photoredox system, relying on decatungstate/disulfide catalysts, for the hydrofunctionalization of styrenes. In this methodology the use of disulfide as a cocatalyst was shown to be crucial for the reaction efficiency. This photoredox system was employed for the hydro-carbamoylation, -acylation, -alkylation, and -silylation of styrenes, giving access to a large variety of useful building blocks and high-value molecules such as amides and unsymmetrical ketones from simple starting materials.

FERROPTOSIS INHIBITORS–DIARYLAMINE PARA-ACETAMIDES

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Paragraph 01365-01366, (2021/09/11)

Provided are compounds that inhibit ferroptosis activity, or modulate or inhibit a disease associated with ferroptosis dysregulation, such as neuropathy, ischemia reperfusion injury, acute kidney failure and cancer, including corresponding sulfonamides, and pharmaceutically acceptable salts, hydrates and stereoisomers thereof. The compounds are employed in pharmaceutical compositions, and methods of making and use, including treating a person in need thereof with an effective amount of the compound or composition, and detecting a resultant improvement in the person's health or condition.

Diketopyrrolopyrrole derivative and application thereof

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Paragraph 0078; 0079; 0080, (2018/12/05)

The invention provides a diketopyrrolopyrrole derivative and application thereof as well as relates to a diketopyrrolopyrrole derivative. The structural formula of the diketopyrrolopyrrole derivativeis as shown in a formula (I): the formula (I) is as shown in the description; in the formula (I), R1 is selected from a group as shown in a formula (I-a), a formula (I-b), a formula (I-c), a formula (I-d) or a formula (I-e) (the formulas are as shown in the description); and in the formula (I-a), the formula (I-b), the formula (I-c), the formula (I-d) and the formula (I-e), * shows connection position. The diketopyrrolopyrrole derivative has excellent photoelectric property and can be applied in the field of organic photoelectric functional devices.

Niacin Receptor Agonists, Compositions Containing Such Compounds and Methods of Treatment

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Page/Page column 38, (2009/04/24)

The present invention encompasses compounds of Formula I: as well as pharmaceutically acceptable salts and hydrates thereof, that are useful for treating atherosclerosis, dyslipidemias and the like. Pharmaceutical compositions and methods of use are also included.

Aminoalcohol derivatives

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Page/Page column 19, (2010/02/12)

The present invention relates to a compound formula[I]: wherein X is bond, —CH2—, —O— or —NH—, R1 and R12 are each independently hydrogen, halogen, lower alkyl, etc., R2 is hydrogen or optionally substituted lower alkyl, R3 is hydrogen or an amino protective group, R4, R5 and R6 are each independently hydrogen or optionally substituted lower alkyl, R7 is -Z-R13, in which Z is bond, etc., and R13 is carboxy, lower alkoxycarbonyl, (lower alkylsulfonyl)carbamoyl or lower alkanoylsulfamoyl, R8 is —Y—R9, in which Y is bond, —CH2—, —O—, —S—, etc., and R9 is hydrogen, lower alkyl, cyclo(lower)alkyl, etc., and R11 is hydrogen, lower alkyl, lower alkoxy, etc., or a salt thereof. The compound [I] of the present invention and pharmaceutically acceptable salts thereof are useful for the prophylactic and/or the therapeutic treatment of pollakiurea or urinary incontinence.

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