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56108-12-4

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56108-12-4 Usage

General Description

4-tert-Butylbenzamide is a chemical compound with the molecular formula C11H15NO. It is a white to light brown crystalline solid that is commonly used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. 4-TERT-BUTYLBENZAMIDE is known for its use as a reagent in organic synthesis and as a starting material in the preparation of functionalized derivatives of benzamides. It has applications in the production of pesticides, dyes, and pharmaceuticals, and is also used as a building block for the manufacture of other organic chemicals. 4-tert-Butylbenzamide is considered to be non-toxic and is generally regarded as safe for use in the specified applications.

Check Digit Verification of cas no

The CAS Registry Mumber 56108-12-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,1,0 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 56108-12:
(7*5)+(6*6)+(5*1)+(4*0)+(3*8)+(2*1)+(1*2)=104
104 % 10 = 4
So 56108-12-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO/c1-11(2,3)9-6-4-8(5-7-9)10(12)13/h4-7H,1-3H3,(H2,12,13)

56108-12-4 Well-known Company Product Price

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  • Alfa Aesar

  • (A15380)  4-tert-Butylbenzamide, 98%   

  • 56108-12-4

  • 10g

  • 461.0CNY

  • Detail
  • Alfa Aesar

  • (A15380)  4-tert-Butylbenzamide, 98%   

  • 56108-12-4

  • 50g

  • 1937.0CNY

  • Detail
  • Alfa Aesar

  • (A15380)  4-tert-Butylbenzamide, 98%   

  • 56108-12-4

  • 250g

  • 8229.0CNY

  • Detail

56108-12-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(tert-Butyl)benzamide

1.2 Other means of identification

Product number -
Other names 4-TERT-BUTYLBENZAMIDE

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:56108-12-4 SDS

56108-12-4Relevant articles and documents

A “universal” catalyst for aerobic oxidations to synthesize (hetero)aromatic aldehydes, ketones, esters, acids, nitriles, and amides

Bartling, Stephan,Beller, Matthias,Chandrashekhar, Vishwas G.,Jagadeesh, Rajenahally V.,Rabeah, Jabor,Rockstroh, Nils,Senthamarai, Thirusangumurugan

supporting information, p. 508 - 531 (2022/02/11)

Functionalized (hetero)aromatic compounds are indispensable chemicals widely used in basic and applied sciences. Among these, especially aromatic aldehydes, ketones, carboxylic acids, esters, nitriles, and amides represent valuable fine and bulk chemicals, which are used in chemical, pharmaceutical, agrochemical, and material industries. For their synthesis, catalytic aerobic oxidation of alcohols constitutes a green, sustainable, and cost-effective process, which should ideally make use of active and selective 3D metals. Here, we report the preparation of graphitic layers encapsulated in Co-nanoparticles by pyrolysis of cobalt-piperazine-tartaric acid complex on carbon as a most general oxidation catalyst. This unique material allows for the synthesis of simple, functionalized, and structurally diverse (hetero)aromatic aldehydes, ketones, carboxylic acids, esters, nitriles, and amides from alcohols in excellent yields in the presence of air.

Application of acylthiourea compound in preparation of medicines for resisting enterovirus

-

Paragraph 0053-0056, (2021/11/03)

The invention discloses an application of an acylthiourea compound in preparation of an anti-enterovirus drug, and belongs to the technical field of medicines. The structure of the acylthiourea compound of the present invention is as shown in the general

Unlocking Amides through Selective C–N Bond Cleavage: Allyl Bromide-Mediated Divergent Synthesis of Nitrogen-Containing Functional Groups

Govindan, Karthick,Chen, Nian-Qi,Chuang, Yu-Wei,Lin, Wei-Yu

supporting information, p. 9419 - 9424 (2021/11/30)

We report a new set of reactions based on the unlocking of amides through simple treatment with allyl bromide, creating a common platform for accessing a diverse range of nitrogen-containing functional groups such as primary amides, sulfonamides, primary amines, N-acyl compounds (esters, thioesters, amides), and N-sulfonyl esters. The method has potential industrial applicability, as demonstrated through gram-scale syntheses in batch and in a continuous flow system.

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