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17852-28-7

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17852-28-7 Usage

Description

2-amino-5-methylbenzophenone is an aromatic ketone belonging to the class of organic compounds. It is characterized by the molecular formula C14H13NO and a molecular weight of 211.26 g/mol. 2-amino-5-methylbenzophenone is known for its role as an intermediate in the synthesis of various products, including pharmaceuticals, dyes, and other organic compounds.

Uses

Used in Pharmaceutical Industry:
2-amino-5-methylbenzophenone is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs and medicinal compounds.
Used in Dye Industry:
In the dye industry, 2-amino-5-methylbenzophenone is utilized as an intermediate in the production of dyes, where its chemical properties are essential for creating colorants with specific characteristics.
Used in Cosmetic Industry:
2-amino-5-methylbenzophenone is used as a UV filter in sunscreen formulations to protect the skin from harmful UV radiation. It effectively absorbs UVB and short UVA rays, making it a valuable ingredient in sunscreen products. However, its use in cosmetic products is strictly regulated due to potential toxicity and environmental concerns.
Safety and Handling:
It is crucial to handle 2-amino-5-methylbenzophenone with care and adhere to safety guidelines when working with this compound to mitigate any risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 17852-28-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,5 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17852-28:
(7*1)+(6*7)+(5*8)+(4*5)+(3*2)+(2*2)+(1*8)=127
127 % 10 = 7
So 17852-28-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H13NO/c1-10-7-8-13(15)12(9-10)14(16)11-5-3-2-4-6-11/h2-9H,15H2,1H3

17852-28-7 Well-known Company Product Price

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  • Aldrich

  • (JWP00339)  (2-Amino-5-methyl-phenyl)-phenyl-methanone  AldrichCPR

  • 17852-28-7

  • JWP00339-1G

  • 4,186.26CNY

  • Detail

17852-28-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-amino-5-methylphenyl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names 2-Amino-5-methyl-benzophenon

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:17852-28-7 SDS

17852-28-7Relevant articles and documents

One-Pot Synthesis of 2-Aminobenzophenones from 2-Alkynyl Arylazides Catalyzed by Pd and Cu Precursors

Fan, Hui,Xu, Shijie,Yang, Fan,Zhang, Xiaoxiang,Zhao, Xuechun

supporting information, p. 4555 - 4558 (2021/08/30)

We describe a novel one-pot three-step reaction of 2-alkynyl arylazides through palladium-catalyzed formation of 3-hydroxy-3-phenylindolin-2-ones followed by hydrolysis of amide bonds and copper-catalyzed decarboxylation to give 2-aminobenzophenones. This synthetic method works well with various 2-alkynyl arylazides and affords the products in moderate to good yields under mild reaction conditions.

Lactam Compound, Preparation Method and Use thereof

-

Paragraph 0165, (2020/02/14)

Provided is a lactam compound, a tautomer, a stereoisomer, a racemate, a nonequal mixture of enantiomers, a geometric isomer, a solvate, a pharmaceutically acceptable salt thereof, or a solvate of the salt of the compound, and a pharmaceutical composition containing the compound. Also provided are the use of such compounds and their pharmaceutical compositions as drugs, especially as antiviral drugs.

Lewis or Br?nsted acid-catalysed reaction of propargylic alcohol-tethered alkylidenecyclopropanes with indoles and pyrroles for the preparation of polycyclic compounds tethered with indole or pyrrole motif

Wei, Hao-Zhao,Yu, Liu-Zhu,Shi, Min

supporting information, p. 135 - 139 (2019/12/26)

We developed a facile synthetic method to access cyclopenta[b]naphthalene derivatives via the Lewis or Br?nsted acid catalysed cascade nucleophilic addition, electronic cyclization, ring-opening rearrangement of propargylic alcohol-tethered alkylidenecyclopropanes with indole and pyrrole derivatives. The reaction exhibited a broad substrate scope and good functional group tolerance under metal-free conditions, affording the desired products in moderate to good yields.

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