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4-(bromoacetyl)phenyl benzoate is a chemical compound with the molecular formula C15H11BrO3. It is the ester of 4-(bromoacetyl)phenol and benzoic acid, characterized by its white to off-white powder form and sparing solubility in water, but solubility in organic solvents. Due to its structural composition, it holds potential for use in pharmaceutical and agrochemical applications.

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  • 3-hydroxy-N-[(5-methoxy-2-nitro-4-phenylmethoxy-phenyl)methylideneamino]naphthalene-2-carboxamide

    Cas No: 5324-15-2

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  • 5324-15-2 Structure
  • Basic information

    1. Product Name: 4-(bromoacetyl)phenyl benzoate
    2. Synonyms: 4-(Bromoacetyl)phenyl benzoate; ethanone, 1-[4-(benzoyloxy)phenyl]-2-bromo-
    3. CAS NO:5324-15-2
    4. Molecular Formula: C15H11BrO3
    5. Molecular Weight: 319.15
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5324-15-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 433.5°C at 760 mmHg
    3. Flash Point: 216°C
    4. Appearance: N/A
    5. Density: 1.466g/cm3
    6. Vapor Pressure: 1.02E-07mmHg at 25°C
    7. Refractive Index: 1.612
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 4-(bromoacetyl)phenyl benzoate(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-(bromoacetyl)phenyl benzoate(5324-15-2)
    12. EPA Substance Registry System: 4-(bromoacetyl)phenyl benzoate(5324-15-2)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 5324-15-2(Hazardous Substances Data)

5324-15-2 Usage

Uses

Used in Organic Synthesis:
4-(bromoacetyl)phenyl benzoate is utilized as a solvent or intermediate in organic synthesis processes, facilitating the creation of various complex organic compounds.
Used in Pharmaceutical Applications:
Due to its structural properties, 4-(bromoacetyl)phenyl benzoate is considered for use in the pharmaceutical industry, potentially contributing to the development of new drugs or drug formulations.
Used in Agrochemical Applications:
4-(bromoacetyl)phenyl benzoate's potential extends to agrochemicals, where it may be employed in the development of pesticides or other agricultural chemicals to improve crop protection and yield.
It is important to handle 4-(bromoacetyl)phenyl benzoate with care, storing it in a cool, dry place away from heat and flame to ensure safety and maintain its properties.

Check Digit Verification of cas no

The CAS Registry Mumber 5324-15-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,2 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5324-15:
(6*5)+(5*3)+(4*2)+(3*4)+(2*1)+(1*5)=72
72 % 10 = 2
So 5324-15-2 is a valid CAS Registry Number.

5324-15-2SDS

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 BENZOIC ACID, 4-(2-BROMOACETYL)PHENYL ESTER

1.2 Other means of identification

Product number -
Other names 4-Bromacetyl-benzolsulfonsaeure-dimethylamid

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:5324-15-2 SDS

5324-15-2Relevant articles and documents

Cascade Functionalization of C(sp3)-Br/C(sp2)-H Bonds: Access to Fused Benzo[ e]isoindole-1,3,5-trione via Visible-Light-Induced Reductive Radical Relay Strategy

Zhu, Jia-Nan,Wang, Wen-Kang,Zhu, Yuan,Hu, Yin-Qiu,Zhao, Sheng-Yin

, p. 6270 - 6274 (2019)

A reductive radical relay strategy for the construction of fused benzo[e]isoindole-1,3,5-trione through a reaction of α-bromo ketones with maleimides in the presence of Ir(ppy)3 under visible-light irradiation is described. The protocol employs very mild reaction conditions and offers satisfactory yields. Moreover, the reaction proceeds through a cascade C(sp3)-Br/C(sp2)-H functionalization, double C-C bond formation, and oxidative aromatization sequence.

Design, synthesis and anti-HIV evaluation of 5-alkyl- 6-(benzo[d][1,3]dioxol-5-alkyl)-2-mercaptopyrimidin-4(3H)-ones as potent HIV-1 NNRTIs

Cui, Yi-Man,He, Yan-Ping,Huang, Si-Ming,Li, Sui-Yuan,Li, Xiao-Li,Li, Yi-Ming,Luo, Rong-Hua,Ni, Dong-Xuan,Tang, E.,Xiao, Wei-Lie,Yang, Liu-Meng,Zhang, Hong-Bin,Zhang, Rui-Han,Zhang, Xing-Jie,Zheng, Yong-Tang,Zheng, Yu-Gui

, (2020/07/21)

In order to discover and develop the new HIV-1 NNRTIs, a series of 5-alkyl-6-(benzo[d][1,3]dioxol-5-ylalkyl)-2-mercaptopyrimidin-4(3H)-ones was synthesized and screened for their in vitro cytotoxicity against HIV-1. Most of the compounds we synthetized sh

Stereoselective synthesis of cis-2,6-disubstituted morpholines and 1,4-oxathianes by intramolecular reductive etherification of 1,5-diketones

Gharpure, Santosh J.,Anuradha, Dandela,Prasad, Jonnalagadda V. K.,Rao, Pidugu Srinivasa

, p. 86 - 90 (2015/01/16)

A simple and efficient, Lewis acid catalysed reductive etherification strategy for the stereoselective synthesis of cis-2,6- disubstituted morpholines and 1,4-oxathianes starting from readily available 1,5-diketones has been developed. The strategy is used in the total synthesis of morpholine-based natural products (±)-chelonin A and formal total synthesis of (±)-chelonin C.

USE OF NOVEL COMPOUND HAVING AFFINITY FOR AMYLOID, AND PROCESS FOR PRODUCTION OF THE SAME

-

, (2010/08/18)

The invention provides a reagent for detecting amyloid in a biological tissue which can detect amyloid in vitro and in vivo with high sensitivity using a compound which has affinity with amyloid and is suppressed in toxicity such as mutagenicity. The reagent for detecting amyloid deposited in a biological tissue comprises the compound represented by the following formula (1) or a salt thereof: wherein A1, A2, A3 and A4 independently represent a carbon or a nitrogen, and R3 is a group represented by the following formula: wherein R1 is a radioactive halogen substituent; m is an integer of 0 to 4; and n is an integer of 0 or 1, provided that at least one of A1, A3, A3 and A4 represents a carbon, and R5 binds to a carbon represented by A1, A2, A3 or A4.

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