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1-isopropylhydrazinecarbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58605-87-1

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58605-87-1 Usage

Hydrazine derivative

The compound contains a central nitrogen atom bonded to two hydrogen atoms, and another carbon atom bonded to nitrogen and a carbonitrile group.

Pharmaceutical industry use

1-isopropylhydrazinecarbonitrile is primarily used as an intermediate in the synthesis of various drugs.

Research and development

The compound can be used in research and development processes for the creation of new pharmaceutical compounds.

Versatile chemical compound

1-isopropylhydrazinecarbonitrile has a wide range of potential applications in various fields due to its unique properties and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 58605-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,6,0 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 58605-87:
(7*5)+(6*8)+(5*6)+(4*0)+(3*5)+(2*8)+(1*7)=151
151 % 10 = 1
So 58605-87-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H9N3/c1-4(2)7(6)3-5/h4H,6H2,1-2H3

58605-87-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-dimethyl-2-(1-phenyltetrazol-5-yl)sulfanylpyridine-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 4,6-dimethyl-2-[(1-phenyl-1h-tetrazol-5-yl)sulfanyl]nicotinonitrile

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:58605-87-1 SDS

58605-87-1Relevant academic research and scientific papers

METHODS OF TREATMENT WITH AMINOLEVULINIC ACID SYNTHASE 2 (ALAS2) MODULATORS

-

Paragraph 00164, (2020/12/29)

Described herein is a compound of Formula I or a pharmaceutically acceptable salt thereof: wherein Ring A R1, R2, a, b, and n are as defined herein. Also described is a method of treating a subject having a disorder in need of treatment, comprising inhibiting aminolevulinic acid synthase 2 (ALAS2) in the subject by administering a compound of Formula (I) or a pharmaceutically acceptable salt thereof. Disorders that are of particular interest are blood disorders, such as porphyria and anemia.

Acyclic cyanamide-based inhibitors of cathepsin K

Barrett, David G.,Deaton, David N.,Hassell, Anne M.,McFadyen, Robert B.,Miller, Aaron B.,Miller, Larry R.,Payne, J. Alan,Shewchuk, Lisa M.,Willard Jr., Derril H.,Wright, Lois L.

, p. 3039 - 3043 (2007/10/03)

Conversion of the proline-derived cyanamide lead to an acyclic cyanamide capable of forming an additional hydrogen bond with cathepsin K resulted in a large increase in inhibitory activity. An X-ray structure of a co-crystal of a cyanamide with cathepsin K confirmed the enzyme interaction. Furthermore, a representative acyclic cyanamide inhibitor 6r was able to attenuate bone resorption in the rat calvarial model.

Process for the production of 1,2,4-triazole derivatives

-

, (2008/06/13)

Process for the production of 1-alkyl-3-hydroxy-5-chloro-1,2,4-triazoles wherein an alkylhydrazine is reacted in an inert solvent in the presence of an acid binding agent with cyanogen chloride to 1-alkyl-1-cyanohydrazine which is subsequently cyclized with phosgene.

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