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1151-94-6

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1151-94-6 Usage

Uses

4-Methoxy-4'-nitrobenzophenone is used as an organic chemical synthesis intermediate.

Preparation

Obtained by reaction of p-nitrobenzoyl chloride with anisole,in the presence of MoO? 2Cl2 (20 mol%) at reflux for 20 h (3%) in the presence of perfluorobutane sulfonic acid in the presence of aluminium chloride in carbon disulfide for 1 h at r.t. (72%) in the presence of MoO? 2Cl2 (20 mol%) at reflux for 20 h (31%).

Check Digit Verification of cas no

The CAS Registry Mumber 1151-94-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,5 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1151-94:
(6*1)+(5*1)+(4*5)+(3*1)+(2*9)+(1*4)=56
56 % 10 = 6
So 1151-94-6 is a valid CAS Registry Number.

1151-94-6 Well-known Company Product Price

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  • Alfa Aesar

  • (B22720)  4-Methoxy-4'-nitrobenzophenone, 97%   

  • 1151-94-6

  • 1g

  • 332.0CNY

  • Detail
  • Alfa Aesar

  • (B22720)  4-Methoxy-4'-nitrobenzophenone, 97%   

  • 1151-94-6

  • 5g

  • 1010.0CNY

  • Detail
  • Alfa Aesar

  • (B22720)  4-Methoxy-4'-nitrobenzophenone, 97%   

  • 1151-94-6

  • 25g

  • 3677.0CNY

  • Detail

1151-94-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methoxyphenyl)-(4-nitrophenyl)methanone

1.2 Other means of identification

Product number -
Other names (4-methoxyphenyl)(4-nitrophenyl)methanone

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:1151-94-6 SDS

1151-94-6Relevant articles and documents

Highly selective catalytic Friedel-Crafts acylation and sulfonylation of activated aromatic compounds using indium metal

Jang, Doo Ok,Moon, Kyung Soo,Cho, Dae Hyan,Kim, Joong-Gon

, p. 6063 - 6066 (2006)

The Friedel-Crafts acylation of activated benzenes with various aromatic and aliphatic acid chlorides was studied in the presence of indium metal. The reaction was accomplished in high isolated yields under solvent or solvent-less conditions. The method is also applicable for preparing diaryl sulfones from aromatic compounds and aryl sulfonyl chlorides.

Liquid-Phase Total Synthesis of Plecanatide Aided by Diphenylphosphinyloxyl Diphenyl Ketone (DDK) Derivatives

Chang, Ninghui,Chao, Jie,Li, Haidi,Li, Jun,Qin, Chuanguang,Tian, Guang,Zhang, Zixin

, p. 3323 - 3328 (2020)

Plecanatide is an oral guanylate cyclase-C agonist for the treatment of gastrointestinal disorders. The large-scale supply of plecanatide is restrained primarily by its industrial manufacture. Herein we developed diphenylphosphinyloxyl diphenyl ketone (DD

Inducing apoptosis through upregulation of p53: structure–activity exploration of anthraquinone analogs

Agbowuro, Ayodeji A.,Anifowose, Abiodun,Lu, Wen,Tan, Chalet,Tripathi, Ravi,Wang, Binghe,Yang, Xiaoxiao

, p. 1199 - 1210 (2020/06/17)

We previously reported a series of p53-elevating anthraquinone compounds with considerable cytotoxicity for acute lymphoblastic leukemia (ALL) cells. To further develop this class of compounds, we examined the effect of a few key structural features on the anticancer structure–activity relationship (SAR) in ALL cells. The active analogs showed comparable cytotoxicity and upregulation of p53 but did not induce significant downregulation of MDM2 as seen with the lead compound AQ-101, indicating the importance of the anthraquinone core scaffold for MDM2 regulation. The result from the current study not only contributes to the SAR framework of these anthraquinone derivatives but also opens up new chemical space for further optimization work.

Recyclable polyetheretherketone fiber-supported N-heterocyclic carbene catalysts for nucleophilic acylation of fluorobenzenes

Shi, Xian-Lei,Sun, Benyu,Hu, Qianqian,Liu, Kun,Li, Pengyu,Wang, Juanjuan

supporting information, p. 11390 - 11393 (2020/10/12)

We report for the first time a novel support of polyetheretherketone fiber for the synthesis of recyclable N-heterocyclic carbene (NHC) catalysts. The fiber catalysts were verified in nucleophilic acylation of fluorobenzenes with superior catalytic activities, and successfully recycled by a tiny pair of tweezers over 21 cycles with minimal loss of performance.

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