15482-69-6

• 

• Basic information

  1. Product Name: (5-BROMO-1-BENZOFURAN-2-YL)(PHENYL)METHANONE
  2. Synonyms: TIMTEC-BB SBB009936;(5-BROMO-1-BENZOFURAN-2-YL)(PHENYL)METHANONE;2-BENZOYL-5-BROMO BENZOFURAN;BUTTPARK 153\33-79;5-BROMO-2-BENZOYLBENZOFURAN;(5-bromo-2-benzofuranyl)-phenylmethanone;(5-bromobenzofuran-2-yl)-phenyl-methanone
  3. CAS NO:15482-69-6
  4. Molecular Formula: C₁₅H₉BrO₂
  5. Molecular Weight: 301.13
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 15482-69-6.mol
  9. Article Data: 12

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: /
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: (5-BROMO-1-BENZOFURAN-2-YL)(PHENYL)METHANONE(CAS DataBase Reference)
  10. NIST Chemistry Reference: (5-BROMO-1-BENZOFURAN-2-YL)(PHENYL)METHANONE(15482-69-6)
  11. EPA Substance Registry System: (5-BROMO-1-BENZOFURAN-2-YL)(PHENYL)METHANONE(15482-69-6)

• 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: 15482-69-6(Hazardous Substances Data)

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• (5-BROMO-1-BENZOFURAN-2-YL)(PHENYL)METHANONE

  Cas No: 15482-69-6

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• (5-BROMO-1-BENZOFURAN-2-YL)(PHENYL)METHANONE

  Cas No: 15482-69-6

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• ZHEJIANG JIUZHOU CHEM CO.,LTD
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• (5-Bromobenzofuran-2-yl)(phenyl)methanone

  Cas No: 15482-69-6

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• 10 Milligram

• Amadis Chemical Co., Ltd.
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15482-69-6 Usage

General Description

(5-Bromo-1-benzofuran-2-yl)(phenyl)methanone is a chemical compound with a benzofuran ring system and a ketone functionality attached to a phenyl group. It is commonly used in organic synthesis and pharmaceutical research. The presence of the bromine and benzofuran moieties make this compound useful for drug discovery, as they can enhance biological activity and interactions with specific biological targets. Additionally, the phenyl group can provide opportunities for further derivatization and modification of the molecule's properties. The compound has potential applications in the development of new drugs, agrochemicals, and materials science. It is important to handle and use this compound with caution, in accordance with proper safety protocols and regulations.

Check Digit Verification of cas no

The CAS Registry Mumber 15482-69-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,8 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15482-69:
(7*1)+(6*5)+(5*4)+(4*8)+(3*2)+(2*6)+(1*9)=116
116 % 10 = 6
So 15482-69-6 is a valid CAS Registry Number.

15482-69-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name	(5-bromo-1-benzofuran-2-yl)-phenylmethanone

1.2 Other means of identification

Product number	-
Other names	5-bromo-2-benzoyl-benzofuran

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:15482-69-6 SDS

15482-69-6Upstream product

• 1761-61-1 5-bromosalicyclaldehyde 
• 98-86-2 acetophenone 
• 18287-99-5 (E)-3-(5-bromo-2-hydroxyphenyl)-1-phenylprop-2-en-1-one 
• 532-27-4 1-chloroacetophenone 
• 70-11-1 α-bromoacetophenone 
• 4636-16-2 iodoacetophenone 
• 644-78-0 2-hydroxychalcone 

15482-69-6Downstream Products

• 1262243-50-4 (R)-(5-bromobenzofuran-2-yl)(phenyl)methanol 
• 82158-29-0 (5-bromobenzofuran-2-yl)(phenyl)methanol 

15482-69-6Relevant articles and documents

Reaction of chalcones with NBS, a simple one pot synthesis of 2-aroylbenzo[b]furanes

Litkei, Gyoergy,Gulacsi, Katalin,Antus, Sandor,Dinya, Zoltan

, p. 3061 - 3074 (1996)

A simple one pot synthesis of 2-aroylbenzo[b]furanes has been achieved by bromomethoxylation with NBS and subsequent treatment of the appropriately substituted 2-hydroxychalcones with sodium hydroxide.

Copper(I)-Catalyzed Chemoselective Reduction of Benzofuran-2-yl Ketones to Alcohols with B2pin2 via a Domino-Borylation-Protodeboronation Strategy

Xuan, Qingqing,Kong, Weiguang,Song, Qiuling

, p. 7602 - 7607 (2017/07/26)

A novel copper(I)-catalyzed chemoselective reduction of the carbonyls of benzofuran-2-yl ketones over furan rings with B2pin2 has been developed. This reaction proceeded under mild conditions. High valuable secondary alcohol derivatives of benzofurans were obtained in good to excellent yields with a broad substrate scope. The mechanistic studies suggested that a domino-borylation-protodeboronation pathway was involved in this reaction.

Synthesis and antitubercular activity of 4-thiazolidinone derivatives incorporating benzofuran moiety

Basawaraj, Raga,Channamma,Sangmeshwar

, p. 59 - 66 (2019/01/21)

5-Bromo-1-benzofuran-2-yl(substituted phenyl) methanones (2a-e) were prepared by the reaction of 2-bromo-1-(phenyl) ethanones and 5-bromosalicylaldehyde in dimethylformamide in the presence of anhydrous potassium carbonate to maintain basic condition. Con

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