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15150-25-1

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15150-25-1 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 77, p. 5440, 1955 DOI: 10.1021/ja01625a085

Check Digit Verification of cas no

The CAS Registry Mumber 15150-25-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,5 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15150-25:
(7*1)+(6*5)+(5*1)+(4*5)+(3*0)+(2*2)+(1*5)=71
71 % 10 = 1
So 15150-25-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N2O/c9-6-10-8(11)7-4-2-1-3-5-7/h1-5H,(H,10,11)

15150-25-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-cyanobenzamide

1.2 Other means of identification

Product number -
Other names N-cyano-benzamide

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:15150-25-1 SDS

15150-25-1Relevant articles and documents

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Ambelang,Johnson

, p. 632 (1939)

-

-

Skinner,Vogt

, p. 5440 (1955)

-

COMPOSITIONS AND METHODS COMPRISING SUBSTITUTED 2-AMINOIMIDAZOLES

-

Paragraph 0208; 0211, (2018/10/25)

The present invention presents 2-(acylamino)imidazoles with therapeutic activity, including selective activity against cancer cells, and compositions comprising them. Methods of using and preparing the 2-(acylamino)imidazoles are also presented.

Copper(I)-catalyzed cascade synthesis of 2-arylsulfanyl-arylcyanamides

Sahoo, Santosh K.,Jamir, Latonglila,Guin, Srimanta,Patel, Bhisma K.

experimental part, p. 2538 - 2548 (2010/12/29)

We have developed a ligand-assisted copper(I)-catalyzed two sequential heteroarylation sequence. An intramolecular S-arylation is followed by an intermolecular N-arylation leading to the direct synthesis of N-aryl-2-aminobenzothiazoles. In most cases however, the 2-arylsulfanyl- arylcyanamide was the major product obtained via an intramolecular C-S bond formation, associated with C-S bond breakage, followed by an intermolecular S-arylation. The selectivity of this ligand-assisted reaction is quite different as compared to that of ligand-free reactions and the rates are much faster giving good yields of products. Various cyanamides can be prepared in excellent yields from their corresponding 1-substituted thioureas with or without the assistance of a ligand with a catalytic quantity of copper(I).

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