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2-Hydroxy-3-(aminomethyl)pyridine hydrochloride is an organic compound that serves as an intermediate in the synthesis of pharmaceuticals. It is characterized by the presence of a hydroxyl group and an aminomethyl group attached to a pyridine ring, with a hydrochloride counterion. 2-Hydroxy-3-(aminomethyl)pyridine hydrochloride plays a crucial role in the development of therapeutic agents targeting specific receptors.

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  • 85468-38-8 Structure
  • Basic information

    1. Product Name: 2-Hydroxy-3-(aminomethyl)pyridine hydrochloride
    2. Synonyms: 2-Hydroxy-3-(aminomethyl)pyridine hydrochloride;3-(aminomethyl)pyridin-2(1H)-onehydrochloride;3-(AMINOMETHYL)PYRIDIN-2(1H)-ONE HYDROCHLORIDE,PURITY:95% MIN(HPLC);2-HYDROXY-3-(AMINOMETHYL)PYRIDINE HCL;3-(aminomethyl)pyridine-2(1H)-one hydrochloride;3-(AMinoMethyl)-2(1H)-pyridinone Hydrochloride;3-(aMinoMethyl)pyridin-2-ol hydrochloride;3-(AMinoMethyl)-2(1H)-pyridinone Monohydrochloride
    3. CAS NO:85468-38-8
    4. Molecular Formula: C6H9ClN2O
    5. Molecular Weight: 160.6
    6. EINECS: N/A
    7. Product Categories: pyridine;Amines;Aromatics;Heterocycles;Intermediates;Intermediates & Fine Chemicals;Pharmaceuticals
    8. Mol File: 85468-38-8.mol
  • Chemical Properties

    1. Melting Point: 181-184 °C
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: Inert atmosphere,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Hydroxy-3-(aminomethyl)pyridine hydrochloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Hydroxy-3-(aminomethyl)pyridine hydrochloride(85468-38-8)
    11. EPA Substance Registry System: 2-Hydroxy-3-(aminomethyl)pyridine hydrochloride(85468-38-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 85468-38-8(Hazardous Substances Data)

85468-38-8 Usage

Uses

Used in Pharmaceutical Industry:
2-Hydroxy-3-(aminomethyl)pyridine hydrochloride is used as a key intermediate in the synthesis of dihydroindenyl piperazinediones, which are Oxytocin receptor antagonists. These antagonists are valuable for the treatment of various gynecological conditions, such as dysmenorrhea, pre-term labor, and endometriosis. By targeting the Oxytocin receptors, these antagonists help regulate the hormonal balance and alleviate the symptoms associated with these conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 85468-38-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,4,6 and 8 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 85468-38:
(7*8)+(6*5)+(5*4)+(4*6)+(3*8)+(2*3)+(1*8)=168
168 % 10 = 8
So 85468-38-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H8N2O.ClH/c7-4-5-2-1-3-8-6(5)9;/h1-3H,4,7H2,(H,8,9);1H

85468-38-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(aminomethyl)-1H-pyridin-2-one,hydrochloride

1.2 Other means of identification

Product number -
Other names -

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:85468-38-8 SDS

85468-38-8Relevant articles and documents

Reaction of N-(2-Pyridylmethyl)-3,5-dimethylbenzamide and N-(3-Pyridylmethyl)-3,5-dimethylbenzamide N-Oxides with Acetic Anhydride

Brana, Miguel F.,Rodriguez, Maria Luz Lopez

, p. 1297 - 1300 (2007/10/02)

As a continuation of our work on the reaction of N-pyridylmethyl-3,5-dimethylbenzamide N-oxides with acetic anhydride, we now report a study of the reaction of N-(2-pyridylmethyl)-3,5-dimethylbenzamide N-oxide (5) and N-(3-pyridylmethyl)-3,5-dimethylbenzamide N-oxide (6) with acetic anhydride.Compound 5 gave N,N'-di(3,5-dimethylbenzoyl)-1,2-di(2-pyridyl)ethenediamine (7) and 3,5-dimethylbenzamide (8).Compound 6 afforded three products formulated as 2-acetoxy-3-(3,5-dimethylbenzoylaminomethyl)pyridine (12), 3-(3,5-dimethylbenzoylaminomethyl)-2-pyridone (13) and 5-(3,5-dimethylbenzoylaminomethyl)-2-pyridone (14).Analytical and spectral data are presented which support the structures proposed.

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