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1H-Benzotriazole-5-carbonitrile, a chemical compound with the molecular formula C7H4N4, is a white crystalline solid known for its stability and non-reactivity under normal conditions. It serves as an essential intermediate in the synthesis of various pharmaceuticals and agrochemicals, and its versatile applications extend to the metalworking industry as a corrosion inhibitor and in the production of plastics and rubber.

24611-70-9

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24611-70-9 Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
1H-Benzotriazole-5-carbonitrile is used as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals for its ability to facilitate the production of these compounds.
Used in Metalworking Industry:
1H-Benzotriazole-5-carbonitrile is used as a corrosion inhibitor to protect metal surfaces by forming a protective layer, thereby preventing metal degradation and extending the lifespan of metal components.
Used in Plastics and Rubber Production:
1H-Benzotriazole-5-carbonitrile is used as an additive in the manufacturing process of plastics and rubber, enhancing the properties of these materials and contributing to their performance characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 24611-70-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,1 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24611-70:
(7*2)+(6*4)+(5*6)+(4*1)+(3*1)+(2*7)+(1*0)=89
89 % 10 = 9
So 24611-70-9 is a valid CAS Registry Number.

24611-70-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2H-benzotriazole-5-carbonitrile

1.2 Other means of identification

Product number -
Other names 1H-1,2,3-Benzotriazole-5-carbonitrile

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:24611-70-9 SDS

24611-70-9Downstream Products

24611-70-9Relevant academic research and scientific papers

Synthesis of Structurally Diverse Benzotriazoles via Rapid Diazotization and Intramolecular Cyclization of 1,2-Aryldiamines

Faggyas, Réka J.,Sloan, Nikki L.,Buijs, Ned,Sutherland, Andrew

, p. 5344 - 5353 (2019/05/21)

An operationally simple method has been developed for the preparation of N-unsubstituted benzotriazoles by diazotization and intramolecular cyclization of a wide range of 1,2-aryldiamines under mild conditions, using a polymer-supported nitrite reagent and p-tosic acid. The functional group tolerance of this approach was further demonstrated with effective activation and cyclization of N-alkyl, -aryl, and -acyl ortho-aminoanilines leading to the synthesis of N1-substituted benzotriazoles. The synthetic utility of this one-pot heterocyclization process was exemplified with the preparation of a number of biologically and medicinally important benzotriazole scaffolds, including an α-amino acid analogue.

ARYLOAZOL-2-YL CYANOETHYLAMINO COMPOUNDS, METHOD OF MAKING AND METHOD OF USING THEREOF

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Paragraph 0490; 0505, (2014/04/03)

The present invention relates to novel aryloazol-2-yl-cyanoethylamino derivatives of formula (I): wherein R3, R4, R5, R6, R7, P, Q, V, W, X, Y, Z and a are as defined in the description, compositions thereof, processes for their preparation and their uses as pesticides.

ENANTIOMERICALLY ENRICHED ARYLOAZOL-2-YL CYANOETHYLAMINO COMPOUNDS, METHOD OF MAKING AND METHOD OF USING THEREOF

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Page/Page column 44, (2010/06/13)

The present invention relates to novel aryloazol-2-yl-cyanoethylamino derivatives substantially enriched in an enantiomer of formula (I): and compounds of formula (IH) wherein R3, R4, R5, R6, R7, R13a, R13b, R14a, R14b, P, Q, V, W, X, Y, Z and a are as defined in the description, compositions thereof, processes for their preparation and their uses as pesticides.

ARYLOAZOL-2-YL CYANOETHYLAMINO COMPOUNDS, METHOD OF MAKING AND METHOD OF USING THEREOF

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Page/Page column 54, (2009/01/20)

The present invention relates to novel aryloazol-2-yl-cyanoethylamino derivatives of formula (I):wherein R3, R4, R5, R6, R7, P, Q, V, W, X, Y, Z and a are as defined in the description, compositions thereof, processes for their preparation and their uses as pesticides.

HETERO COMPOUND

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Page/Page column 30, (2009/01/24)

[Problems] To provide a useful compound as an active ingredient for a preventing and/or treating agent for rejection in the transplantation of an organ, bone marrow, or a tissue, an autoimmune disease, or the like, which has an excellent S1P1 a

Novel heteroaryl substituted piperidine derivatives which are L-CPT1 inhibitors

-

Page/Page column 42, (2010/11/27)

The invention is concerned with novel substituted piperidine derivatives of formula (I) wherein R1, R2, R3, R4, R5, R6, R7 and X are as defined in the description and in the claims, as well as physiologically acceptable salts and esters thereof. These compounds inhibit L-CPT1 and can be used as medicaments.

Substituted 2-methyl-benzimidazole respiratory syncytial virus antiviral agents

-

, (2008/06/13)

The present invention concerns antiviral compounds, their methods of preparation and their compositions, and use in the treatment of viral infections. More particularly, the invention provides heterocyclic substituted 2-methylbenzimidazole derivatives for the treatment of respiratory syncytial virus infection.

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