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N-(2,2,3,3,3-pentafluoropropyl)benzamide is a synthetic chemical compound with the molecular formula C10H8F5NO. It is a derivative of benzamide, where a pentafluoropropyl group is attached to the nitrogen atom. N-(2,2,3,3,3-pentafluoropropyl)benzamide is characterized by its fluorinated side chain, which can influence its physical and chemical properties, such as solubility, reactivity, and stability. The presence of fluorine atoms in the molecule can enhance its electronegativity and lipophilicity, making it potentially useful in various applications, including pharmaceuticals and materials science. Due to its unique structure, N-(2,2,3,3,3-pentafluoropropyl)benzamide may exhibit different biological activities compared to its non-fluorinated counterparts, and it could be a subject of interest in the development of new drugs or chemical intermediates.

785-33-1

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785-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 785-33-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,8 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 785-33:
(5*7)+(4*8)+(3*5)+(2*3)+(1*3)=91
91 % 10 = 1
So 785-33-1 is a valid CAS Registry Number.

785-33-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2,2,3,3,3-pentafluoro-propyl)-benzamide

1.2 Other means of identification

Product number -
Other names N-(2,2,3,3,3-Pentafluor-propyl)-benzamid

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:785-33-1 SDS

785-33-1Relevant academic research and scientific papers

NaOTs-promoted transition metal-free C-N bond cleavage to form C-X (X = N, O, S) bonds

Chen, Wei,Liu, Sicheng,Liu, Tingting,Majeed, Irfan,Ye, Xiaojing,Zeng, Zhuo,Zhang, Yuqi,Zhu, Yulin

, p. 8566 - 8571 (2021/10/20)

Multifunctional transformation of amide C-N bond cleavage is reported. The protocol applies to benzamide, thioamide, alcohols, and mercaptan under similar reaction conditions catalyzed by NaOTs. It is noteworthy that NaOTs can not only be recycled and reused for up to three cycles without significant loss in catalytic activity, but also catalyze gram-grade reactions. This study provides a novel solution with mild conditions and a simple procedure for transformation of multiple amides.

Biomimetic reductive amination of perfluoroalkylcarboxylic acids to α,α-dihydroperfluoroalkylamines

Soloshonok, Vadim A,Ohkura, Hironari,Uneyama, Kenji

, p. 5449 - 5452 (2007/10/03)

The first general method for the reducing reagent-free, biomimetic transformation of perfluorocarboxylic acids to the α,α-dihydroperfluoroalkyl amines is reported. High chemical yields and simplicity of the experimental procedure render this method immediately useful and synthetically superior to the conventional approaches relying on application of reducing reagents.

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