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17174-98-0

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17174-98-0 Usage

General Description

2-Cyanobenzamide is a chemical compound with the formula C8H6N2O. It is a benzamide derivative with a cyano group attached to the benzene ring. 2-CYANOBENZAMIDE is a white solid at room temperature, and it is sparingly soluble in water but soluble in organic solvents. 2-Cyanobenzamide has been widely used as a building block in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It is also used as a precursor in the synthesis of various organic compounds due to its reactivity and versatility. Additionally, 2-Cyanobenzamide has been studied for its potential biological and pharmacological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 17174-98-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,7 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17174-98:
(7*1)+(6*7)+(5*1)+(4*7)+(3*4)+(2*9)+(1*8)=120
120 % 10 = 0
So 17174-98-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N2O/c9-5-6-3-1-2-4-7(6)8(10)11/h1-4H,(H2,10,11)

17174-98-0 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (B21596)  2-Cyanobenzamide, 98%   

  • 17174-98-0

  • 1g

  • 317.0CNY

  • Detail
  • Alfa Aesar

  • (B21596)  2-Cyanobenzamide, 98%   

  • 17174-98-0

  • 5g

  • 1227.0CNY

  • Detail

17174-98-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-CYANOBENZAMIDE

1.2 Other means of identification

Product number -
Other names ortho-cyanobenzamide

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:17174-98-0 SDS

17174-98-0Relevant articles and documents

Gordon,Ehrenkaufer

, p. 44 (1971)

Method for preparing derivatives of benzamide under microwave condition in aqueous phase

-

Paragraph 0018; 0102, (2019/03/28)

The invention discloses a method for preparing derivatives of benzamide under a microwave condition in an aqueous phase. A coupling reaction is carried out between substituted benzoic acid and amine under the microwave condition in the aqueous phase. The method for preparing the derivatives of benzamide is environmentally friendly, easy and convenient to operate, safe, low in cost and efficient. Compared with the prior art, the method can be applicable to a large number of functional groups, is high in yield, produces fewer by-products, and further is easy to operate, safe, low in cost and environmentally friendly. A formula is shown in the description.

Modulation of Nitrile Hydratase Regioselectivity towards Dinitriles by Tailoring the Substrate Binding Pocket Residues

Cheng, Zhongyi,Cui, Wenjing,Xia, Yuanyuan,Peplowski, Lukasz,Kobayashi, Michihiko,Zhou, Zhemin

, p. 449 - 458 (2017/12/15)

The regioselective hydration of dinitriles is one of the most attractive approaches to prepare ω-cyanocarboxamides or diamides and such regioselectivity is often beyond the capability of chemical catalysts. The use of nitrile hydratase to biotransform dinitriles selectively would be highly desirable. Molecular docking of two aliphatic dinitriles and two aromatic dinitriles into the active site of a nitrile hydratase (NHase) from Rhodococcus rhodochrous J1 allowed the identification of proximal NHase substrate binding pocket residues. Four residues (βLeu48, βPhe51, βTyr68, and βTrp72) were selected for single- and double-point mutations to modulate the NHase regioselectivity towards dinitriles. Several NHase mutants with an altered regioselectivity were obtained, and the best one was Y68T/W72Y. Docking experiments further indicated that the poor binding affinity of aliphatic and aromatic ω-cyanocarboxamides to the NHase variants resulted in distinct regioselectivity between wild-type and mutated NHases.

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