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5-Amino-2-hydroxybenzonitrile, with the chemical formula C7H6N2O, is a white solid chemical compound that serves as a crucial intermediate in the synthesis of various pharmaceuticals and organic compounds. Known by the trade name Potent, it is utilized in the manufacturing of drugs such as olverembatinib. Classified as a hazardous substance, it requires careful handling and the implementation of proper safety measures to mitigate potential health hazards.

87029-84-3

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87029-84-3 Usage

Uses

Used in Pharmaceutical Industry:
5-Amino-2-hydroxybenzonitrile is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with therapeutic potential.
Used in Organic Synthesis:
In the field of organic chemistry, 5-Amino-2-hydroxybenzonitrile is employed as a versatile building block for the creation of a wide range of organic compounds, highlighting its utility in chemical research and development.
Used in Drug Manufacturing:
Specifically, 5-Amino-2-hydroxybenzonitrile is used in the manufacturing process of olverembatinib, a drug with specific therapeutic applications, underlining its importance in the pharmaceutical sector for drug production.
Safety Measures:
When working with 5-Amino-2-hydroxybenzonitrile, it is imperative to adhere to safety protocols, including the use of protective clothing and gloves, and to ensure that the work environment is well-ventilated to minimize health risks associated with exposure to this hazardous substance.

Check Digit Verification of cas no

The CAS Registry Mumber 87029-84-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,0,2 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87029-84:
(7*8)+(6*7)+(5*0)+(4*2)+(3*9)+(2*8)+(1*4)=153
153 % 10 = 3
So 87029-84-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N2O/c8-4-5-3-6(9)1-2-7(5)10/h1-3,10H,9H2

87029-84-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Amino-2-hydroxybenzonitrile

1.2 Other means of identification

Product number -
Other names BENZONITRILE, 5-AMINO-2-HYDROXY-

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:87029-84-3 SDS

87029-84-3Relevant academic research and scientific papers

Synthesis of functionalized analogs of pyochelin, a siderophore of Pseudomonas aeruginosa and Burkholderia cepacia

Rivault, Freddy,Schons, Viviane,Liébert, Clémence,Burger, Alain,Sakr, Elias,Abdallah, Mohamed A.,Schalk, Isabelle J.,Mislin, Ga?tan L.A.

, p. 2247 - 2254 (2007/10/03)

Using an improved synthesis of pyochelin, a siderophore common to several pathogenic Pseudomonas species, three functionalized pyochelin analogs were efficiently synthesized starting from appropriate 2-hydroxybenzonitriles.

NOVEL AMIDE COMPOUNDS WITH MCH ANTAGONISTIC EFFECT AND MEDICAMENTS COMPRISING SAID COMPOUNDS

-

Page/Page column 88-89, (2008/06/13)

The invention relates to amide compounds of general formula (I), in which the groups and residues A, B, b, W, X, Y, Z, R1, R2 and R3 have the meanings given in claim 1. The invention further relates to medicaments comprising at least one of said amides. Said medicaments are suitable for the treatment of metabolic disorders and/or eating disorders, in particular, obesity, bulimia, anorexia, hyperphagia, and diabetes as a result of the MCH receptor antagonism.

Bacterial siderophores: Synthesis and biological activities of novel pyochelin analogues

Zamri,Schalk,Pattus,Abdallah

, p. 1147 - 1150 (2007/10/03)

The synthesis and biological activities of four pyochelin analogues substituted in different parts of the molecule are reported: 5-NHBoc-pyochelin, 3″N-Boc-pyochelin, 3″-nor-NH-pyochelin and neopyochelin II, the enantiomer of natural pyochelin. All these

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