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50372-61-7

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50372-61-7 Usage

Description

2,3-Dibromo-5-benzoylpyrrole is an organic compound characterized by its unique molecular structure, featuring a pyrrole ring with two bromine atoms at the 2nd and 3rd positions, and a benzoyl group attached at the 5th position. 2,3-Dibromo-5-benzoylpyrrole is known for its potential applications in various fields due to its chemical properties.

Uses

Used in Pharmaceutical Industry:
2,3-Dibromo-5-benzoylpyrrole is used as an intermediate compound for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs with potential therapeutic applications.
Used in Chemical Synthesis:
In the field of organic chemistry, 2,3-Dibromo-5-benzoylpyrrole is used as a building block for the creation of more complex molecules. Its reactive sites, such as the bromine atoms and the benzoyl group, can be further modified to produce a wide range of chemical products.
Used in Research and Development:
2,3-Dibromo-5-benzoylpyrrole is also utilized in research and development settings, where it can be employed to study various chemical reactions and mechanisms. Its unique properties make it an interesting subject for scientific investigation, potentially leading to new discoveries and advancements in the field of chemistry.
In the provided materials, 2,3-Dibromo-5-benzoylpyrrole is specifically used in the preparation of another compound, 4,5-Dibromo-2-benzoylpyrrole, through a series of chemical reactions involving amidation, Friedel-Crafts reaction, and substitution with Br2. This demonstrates its utility as a starting material in the synthesis of complex organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 50372-61-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,3,7 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 50372-61:
(7*5)+(6*0)+(5*3)+(4*7)+(3*2)+(2*6)+(1*1)=97
97 % 10 = 7
So 50372-61-7 is a valid CAS Registry Number.

50372-61-7SDS

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 (4,5-Dibromo-1H-pyrrol-2-yl)(phenyl)methanone

1.2 Other means of identification

Product number -
Other names (4,5-dibromo-1H-pyrrol-2-yl)-phenylmethanone

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:50372-61-7 SDS

50372-61-7Synthetic route

phenyl(1H-pyrrol-2-yl)methanone
7697-46-3

phenyl(1H-pyrrol-2-yl)methanone

2,3-dibromo-5-benzoylpyrrole
50372-61-7

2,3-dibromo-5-benzoylpyrrole

Conditions
ConditionsYield
With copper(ll) bromide In acetonitrile for 48h; Ambient temperature;85%
With bromine In dichloromethane 0 deg C to RT, 2.5 h;77%
With bromine In dichloromethane76.5%
cycl-isopropylidene cyclopropane-1,1-dicarboxylate
5617-70-9

cycl-isopropylidene cyclopropane-1,1-dicarboxylate

2,3-dibromo-5-benzoylpyrrole
50372-61-7

2,3-dibromo-5-benzoylpyrrole

C19H16Br2NO5(1-)*Na(1+)
80965-17-9

C19H16Br2NO5(1-)*Na(1+)

Conditions
ConditionsYield
With sodium hydride 1.) DMF, RT, 1 h, 2.) 75-80 deg C, 4 h; Multistep reaction;
2,3-dibromo-5-benzoylpyrrole
50372-61-7

2,3-dibromo-5-benzoylpyrrole

Ketorolac
74103-06-3

Ketorolac

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: 1.) NaH / 1.) DMF, RT, 1 h, 2.) 75-80 deg C, 4 h
2: HCl / 5 h / 0 deg C to RT
4: magnesium oxide, H2 / 5percent Pd/C / H2O; methanol / 2 h / 760 Torr / Ambient temperature
View Scheme
2,3-dibromo-5-benzoylpyrrole
50372-61-7

2,3-dibromo-5-benzoylpyrrole

5-benzoyl-7-bromo-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid
84023-60-9

5-benzoyl-7-bromo-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acid

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 1.) NaH / 1.) DMF, RT, 1 h, 2.) 75-80 deg C, 4 h
2: HCl / 5 h / 0 deg C to RT
View Scheme
2,3-dibromo-5-benzoylpyrrole
50372-61-7

2,3-dibromo-5-benzoylpyrrole

methyl 5-benzoyl-7-bromo-1,2-dihydro-3H-pyrrolo<1,2-a>pyrrole-1-carboxylate
80965-19-1

methyl 5-benzoyl-7-bromo-1,2-dihydro-3H-pyrrolo<1,2-a>pyrrole-1-carboxylate

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 1.) NaH / 1.) DMF, RT, 1 h, 2.) 75-80 deg C, 4 h
2: HCl / 5 h / 0 deg C to RT
3: 1.) NaH / 1.) DMF, 20 min, 2.) 75 deg C, 1.5 h
View Scheme
2,3-dibromo-5-benzoylpyrrole
50372-61-7

2,3-dibromo-5-benzoylpyrrole

dimethyl 5-benzoyl-7-bromo-1,2-dihydro-3H-pyrrolo<1,2-a>pyrrole-1,1-dicarboxylate
80965-20-4

dimethyl 5-benzoyl-7-bromo-1,2-dihydro-3H-pyrrolo<1,2-a>pyrrole-1,1-dicarboxylate

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 1.) NaH / 1.) DMF, RT, 1 h, 2.) 75-80 deg C, 4 h
2: HCl / 5 h / 0 deg C to RT
3: 1.) NaH / 1.) DMF, 20 min, 2.) 75 deg C, 1.5 h
View Scheme
2,3-dibromo-5-benzoylpyrrole
50372-61-7

2,3-dibromo-5-benzoylpyrrole

dimethyl[2-(2,3-dibromo-5-benzoylpyrrol-1-yl)ethyl]malonate
80965-18-0

dimethyl[2-(2,3-dibromo-5-benzoylpyrrol-1-yl)ethyl]malonate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 1.) NaH / 1.) DMF, RT, 1 h, 2.) 75-80 deg C, 4 h
2: HCl / 5 h / 0 deg C to RT
View Scheme
spiro[2.5]-5,7-dioxa-6,6-dimethyloctane-4,8-dione

spiro[2.5]-5,7-dioxa-6,6-dimethyloctane-4,8-dione

flurosil

flurosil

2,3-dibromo-5-benzoylpyrrole
50372-61-7

2,3-dibromo-5-benzoylpyrrole

dimethyl[2-(2,3-dibromo-5-benzoylpyrrol-1-yl)ethyl]malonate
80965-18-0

dimethyl[2-(2,3-dibromo-5-benzoylpyrrol-1-yl)ethyl]malonate

Conditions
ConditionsYield
With hydrogenchloride In N-methyl-acetamide; methanol; diethyl ether; mineral oil

50372-61-7Relevant articles and documents

Oxidative Halogenation of Substituted Pyrroles with Cu(II). Part III. Bromination and Chlorination of 2-Benzoylpyrrole

Petruso, S.,Caronna, S.

, p. 355 - 357 (2007/10/02)

The bromination of 2-benzoylpyrrole with copper (II) bromide in the homogenous and heterogenous phase is described, giving 4- and 5-monobromo derivatives whose ratio decreases as the temperature is increased.The same reaction with copper(II) chloride in acetonitrile at 60 deg C produces 5-chloro-2-benzoylpyrrole as the major product. 4,5-Dihalopyrroles in good yields are obtained with an excess of halogenating agent.

Processes for preparing 5-benzoyl-7-halo-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acids

-

, (2008/06/13)

5-benzoyl-7-halo-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acids, represented by the formula STR1 and the pharmaceutically acceptable non-toxic esters and salts thereof, wherein: R is hydrogen or lower alkyl; X is hydrogen, lower alkyl, lower alkoxyl, lower alkoxycarbonyl, carboxyl, lower alkylcarbonyl, sulfonic acid, sulfonic acid alkyl ester, fluoro, chloro, or bromo; and Y is chloro or bromo, which are novel, and 5-benzoyl-1,2-dihydro-3H-pyrrolo[1,2-a]pyrrole-1-carboxylic acids which are represented by the formula STR2 wherein X and R are as above defined except that X cannot be chloro or bromo, are prepared by decarboxylation of the corresponding 1,1 dicarboxylates. Intermediates in said preparation are also disclosed.

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