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Benzamide, N-cyclopropyl(8CI,9CI) is a chemical compound with the molecular formula C9H9NO. It is a derivative of benzamide that features a cyclopropyl group attached to the nitrogen atom. This unique structure and its potential properties make it a compound of interest for organic synthesis and pharmaceutical research. The distinct physiological and biochemical effects it may exhibit compared to other benzamides highlight its value for further investigation and development across various scientific disciplines.

15205-35-3

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15205-35-3 Usage

Uses

Used in Organic Synthesis:
Benzamide, N-cyclopropyl(8CI,9CI) is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of chemical products, making it a valuable component in the field of organic chemistry.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Benzamide, N-cyclopropyl(8CI,9CI) is used as a potential active pharmaceutical ingredient (API). Its distinct properties may lead to the development of new drugs with novel mechanisms of action, offering potential therapeutic benefits in various medical conditions.
Used in Scientific Investigations:
Benzamide, N-cyclopropyl(8CI,9CI) is employed as a research tool in various scientific studies. Its unique characteristics make it an interesting subject for exploring new chemical reactions, understanding molecular interactions, and advancing our knowledge in chemistry and related fields.

Check Digit Verification of cas no

The CAS Registry Mumber 15205-35-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,0 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15205-35:
(7*1)+(6*5)+(5*2)+(4*0)+(3*5)+(2*3)+(1*5)=73
73 % 10 = 3
So 15205-35-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO/c12-10(11-9-6-7-9)8-4-2-1-3-5-8/h1-5,9H,6-7H2,(H,11,12)

15205-35-3SDS

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 N-cyclopropylbenzamide

1.2 Other means of identification

Product number -
Other names Benzoesaeure-cyclopropylamid

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:15205-35-3 SDS

15205-35-3Downstream Products

15205-35-3Relevant academic research and scientific papers

Synthesis of thiochromans via [3+3] annulation of aminocyclopropanes with thiophenols

Wang, Ming-Ming,Jeon, Seongmin,Waser, Jer?me

, p. 9123 - 9127 (2020)

We report the one-pot synthesis of 4-amino thiochromans using simple aminocyclopropanes and thiophenols through a formal [3+3] annulation reaction. This reaction proceeds under mild conditions with good functional group tolerance. The thiochroman core was

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

supporting information, 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.

Benzyne-Mediated Esterification Reaction

Zhao, Jinlong,Shi, Jiarong,Li, Yang

supporting information, p. 7274 - 7278 (2021/10/01)

A benzyne-mediated esterification of carboxylic acids and alcohols under mild conditions has been realized, which is made possible via a selective nucleophilic addition of carboxylic acid to benzyne in the presence of alcohol. After a subsequent transesterification with alcohol, the corresponding esters can be produced efficiently. This benzyne-mediated protocol can be used on the modification of Ibuprofen, cholesterol, estradiol, and synthesis of nandrolone phenylpropionate. In addition, benzyne can also be used to promote lactonization and amidation reaction.

Diamine Synthesis via the Nitrogen-Directed Azidation of σ- And π-C-C Bonds

Nguyen, Tin V. T.,Wang, Ming-Ming,Waser, Jerome

supporting information, p. 11969 - 11975 (2021/08/24)

Diamines are essential building blocks for the synthesis of agrochemicals, drugs, and organic materials, yet their synthesis remains challenging, as both nitrogens need to be differentiated and diverse substitution patterns (1,2, 1,3, or 1,4) are required. We report herein a new strategy giving access to 1,2, 1,3, and 1,4 amido azides as orthogonally protected diamines based on the nitrogen-directed diazidation of alkenes, cyclopropanes, and cyclobutanes. Commercially available copper thiophene-2-carboxylate (CuTc, 2 mol %) as catalyst promoted the diazidation of both πand σ C-C bonds within 10 min in the presence of readily available oxidants and trimethylsilyl azide. Selective substitution of the formed α-amino azide by carbon nucleophiles (electron-rich aromatic, malonate, organosilicon, organoboron, organozinc, and organomagnesium compounds) was then achieved in a one-pot fashion, leading to the formation of 1,2-, 1,3-, and 1,4-diamines with the amino groups protected orthogonally as an amide/carbamate and an azide.

Photocatalyzed Triplet Sensitization of Oximes Using Visible Light Provides a Route to Nonclassical Beckmann Rearrangement Products

Zhang, Xiao,Rovis, Tomislav

supporting information, p. 21211 - 21217 (2021/12/27)

Oximes are valuable synthetic intermediates for the preparation of a variety of functional groups. To date, the stereoselective synthesis of oximes remains a major challenge, as most current synthetic methods either provide mixtures of E and Z isomers or furnish the thermodynamically preferred E isomer. Herein we report a mild and general method to achieve Z isomers of aryl oximes by photoisomerization of oximes via visible-light-mediated energy transfer (EnT) catalysis. Facile access to (Z)-oximes provides opportunities to achieve regio- and chemoselectivity complementary to those of widely used transformations employing oxime starting materials. We show an enhanced one-pot protocol for photocatalyzed oxime isomerization and subsequent Beckmann rearrangement that enables novel reactivity with alkyl groups migrating preferentially over aryl groups, reversing the regioselectivity of the traditional Beckmann reaction. Chemodivergent N- or O- cyclizations of alkenyl oximes are also demonstrated, leading to nitrones or cyclic oxime ethers, respectively.

Synthesis of 1,4-Dihydropyridines and Related Heterocycles by Iodine-Mediated Annulation Reactions of N-Cyclopropyl Enamines

Chang, Junbiao,Fang, Yingchao,Wang, Manman,Wei, Lanlan,Xia, Biao,Yu, Wenquan,Zhao, Yifei,Zhao, Zongxiang

, p. 9625 - 9630 (2021/12/14)

The annulation of N-cyclopropyl enamines to produce 1,4-dihydropyridine (1,4-DHP) derivatives is described. In the presence of molecular iodine (I2), an N-cyclopropyl enamine substrate undergoes iodination, opening of the cyclopropyl ring, and

UV-Light-Induced N-Acylation of Amines with α-Diketones

Xu, Zhihui,Yang, Tianbao,Tang, Niu,Ou, Yifeng,Yin, Shuang-Feng,Kambe, Nobuaki,Qiu, Renhua

supporting information, p. 5329 - 5333 (2021/07/21)

Herein, we develop a mild method for N-acylation of primary and secondary amines with α-diketones induced by ultraviolet (UV) light. Forty-six examples with various functional groups are explored at room temperature with irradiation by three 26 W UV lamps (350-380 nm). The yield reaches 97%. The gram scale experiment product yield is 76%. Moreover, this system can be applied to the synthesis of several amino acid derivatives. Mechanistic studies show that benzoin is generated in situ from benzil under UV irradiation.

Nickel-Catalyzed Photodehalogenation of Aryl Bromides

Higginson, Bradley,Sanjosé-Orduna, Jesus,Gu, Yiting,Martin, Ruben

supporting information, p. 1633 - 1636 (2021/04/23)

Herein, we describe a Ni-catalyzed photodehalogenation of aryl bromides under visible-light irradiation that utilizes tetrahydrofuran as hydrogen source. The protocol obviates the need for exogeneous amine reductants or photocatalysts and is characterized by its simplicity and broad scope, including challenging substrate combinations.

Graphene oxide: A convenient metal-free carbocatalyst for facilitating amidation of esters with amines

Patel, Khushbu P.,Gayakwad, Eknath M.,Shankarling, Ganapati S.

, p. 2661 - 2668 (2020/02/20)

Herein, we report a graphene oxide (GO) catalyzed condensation of non-activated esters and amines, that can enable diverse amides to be synthesized from abundant ethyl esters forming only volatile alcohol as a by-product. GO accelerates ester to amide conversion in the absence of any additives, unlike other catalysts. A wide range of ester and amine substrates are screened to yield the respective amides in good to excellent yields. The improved catalytic activity can be ascribed to the oxygenated functionalities present on the graphene oxide surface which forms H-bonding with the reactants accelerating the reaction. Improved yields and a wide range of functional group tolerance are some of the important features of the developed protocol.

Oxidative Fluorination of Cyclopropylamides through Organic Photoredox Catalysis

Wang, Ming-Ming,Waser, Jér?me

supporting information, p. 16420 - 16424 (2020/07/30)

We report an oxidative ring-opening strategy to transform cyclopropylamides and cyclobutylamides into fluorinated imines. The imines can be isolated in their more stable hemiaminal form, with the fluorine atom installed selectively at the γ or δ position. Both inexpensive benzophenone with UVA light or organic and inorganic dyes with blue light could be used as photoredox catalysts to promote this process. Various fluorinated amines were then obtained by nucleophilic attack on the hemiaminals in one pot, giving access to a broad range of useful building blocks for medicinal chemistry.

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