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Benzeneacetonitrile, 4-amino-2-cyano- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

853910-50-6

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853910-50-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 853910-50-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,3,9,1 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 853910-50:
(8*8)+(7*5)+(6*3)+(5*9)+(4*1)+(3*0)+(2*5)+(1*0)=176
176 % 10 = 6
So 853910-50-6 is a valid CAS Registry Number.

853910-50-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-amino-2-(cyanomethyl)benzonitrile

1.2 Other means of identification

Product number -
Other names 5-amino-2-cyanomethyl-benzonitrile

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:853910-50-6 SDS

853910-50-6Downstream Products

853910-50-6Relevant articles and documents

Reductive domino reaction to access chromeno[2,3-c]isoquinoline-5-amines with antiproliferative activities against human tumor cells

Yue, Xiaoyi,Festa, Alexey A.,Storozhenko, Olga A.,Varlamov, Alexey V.,Subramani, Karthikeyan,Boccarelli, Angelina,Purgatorio, Rosa,Altomare, Cosimo D.,Voskressensky, Leonid G.

, (2020)

An interaction of homophthalonitrile with salicylaldehydes proceeds as a novel domino reaction and results in the formation of nineteen 12H-chromeno[2,3-c]isoquinoline-5-amine derivatives. Four new bonds and two cycles are forged in a single synthetic operation, employing cheap and eco-friendly ammonium formate, acting both as a catalyst and a reducing agent. The in vitro cytotoxicity tests revealed antiproliferative activities against five human tumor cell lines, including the cisplatin-resistant ovarian carcinoma one (A2780cp8), with inhibitory potency data (IC50) in the low micromolar range in most cases. Molecular docking calculations and fluorescence quenching studies revealed possible binding properties with DNA of the active compounds.

1H-IMIDAZO[4,5-C]QUINOLINE DERIVATIVES IN THE TREATMENT OF PROTEIN KINASE DEPENDENT DISEASES

-

Page/Page column 109, (2010/02/12)

The invention relates to the use of imidazoquinolines and salts thereof in the treatment of protein kinase diseases and for the manufacture of pharmaceutical preparations for the treatment of said diseases, imidazoquinolines for use in the treatment of protein kinase dependent diseases, a method of treatment against said diseases, comprising administering the imidazoquinolines to a warm-blooded animal, especially a human, pharmaceutical preparations comprising an imidazoquinoline, especially for the treatment of a protein kinase dependent disease, novel imidazoquinolines, and a process for the preparation of the novel imidazoquinolines.

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