192642-94-7

• 

• Basic information

  1. Product Name: (4-Bromopyridin-2-yl)methyl acetate
  2. Synonyms: (4-Bromopyridin-2-yl)methyl acetate
  3. CAS NO:192642-94-7
  4. Molecular Formula: C₈H₈BrNO₂
  5. Molecular Weight: 230.06
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 192642-94-7.mol
  9. Article Data: 5

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: 275.5°C at 760 mmHg
  3. Flash Point: 120.4°C
  4. Appearance: /
  5. Density: 1.517g/cm³
  6. Vapor Pressure: 0.00508mmHg at 25°C
  7. Refractive Index: 1.545
  8. Storage Temp.: 2-8°C
  9. Solubility: N/A
  10. PKA: 2.39±0.10(Predicted)
  11. CAS DataBase Reference: (4-Bromopyridin-2-yl)methyl acetate(CAS DataBase Reference)
  12. NIST Chemistry Reference: (4-Bromopyridin-2-yl)methyl acetate(192642-94-7)
  13. EPA Substance Registry System: (4-Bromopyridin-2-yl)methyl acetate(192642-94-7)

• 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: 192642-94-7(Hazardous Substances Data)

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• (4-BROMOPYRIDIN-2-YL)METHYL ACETATE

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• 2-Pyridinemethanol,4-bromo-, 2-acetate

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192642-94-7 Usage

General Description

The chemical (4-Bromopyridin-2-yl)methyl acetate is a compound consisting of a bromine-substituted pyridine ring linked to a methyl acetate group. It is commonly used as a building block in organic synthesis, particularly in the pharmaceutical industry for the production of various drug compounds. This chemical is known for its potential as a versatile intermediate for the synthesis of various biologically active molecules. Its unique structure and reactivity make it valuable for the creation of new compounds with potential therapeutic effects. Additionally, (4-Bromopyridin-2-yl)methyl acetate has been studied for its potential use in the field of agrochemicals and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 192642-94-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,6,4 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 192642-94:
(8*1)+(7*9)+(6*2)+(5*6)+(4*4)+(3*2)+(2*9)+(1*4)=157
157 % 10 = 7
So 192642-94-7 is a valid CAS Registry Number.

InChI:InChI=1/C8H8BrNO2/c1-6(11)12-5-8-4-7(9)2-3-10-8/h2-4H,5H2,1H3

192642-94-7SDS

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	(4-bromopyridin-2-yl)methyl acetate

1.2 Other means of identification

Product number	-
Other names	acetic acid 4-bromopyridin-2-ylmethyl ester

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:192642-94-7 SDS

192642-94-7Upstream product

• 100367-74-6 4-bromo-2-methylpyridine N-oxide 
• 108-24-7 acetic anhydride 
• 22282-99-1 4-bromo-2-methylpyridine 
• 502509-20-8 4-bromo-2-vinylpyridine 
• 1120-87-2 4-bromopyridin 
• 131747-45-0 4-bromo-2-(hydroxymethyl)pyridine 

192642-94-7Downstream Products

• 502509-29-7 acetic acid 4-(2-{2-[5-[2-(2-aza-bicyclo[2.2.2]oct-2-yl)-1,1-dimethyl-2-oxo-ethyl]-2-(3,5-dimethyl-phenyl)-1H-indol-3-yl]-propylamino}-ethyl)-pyridin-2-ylmethyl ester 
• 192642-79-8 4-bromopyridine-2-carboxaldehyde tosylhydrazone 
• 192642-77-6 5-bromo-[1,2,3]triazolo[1,5-a]pyridine 
• 131747-63-2 4-bromo-2-pyridinecarboxaldehyde 
• 131747-45-0 4-bromo-2-(hydroxymethyl)pyridine 
• 959756-37-7 acetic acid 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)pyridin-2-ylmethyl ester 

192642-94-7Relevant articles and documents

GPR52 MODULATORS AND METHODS OF USE

-

Page/Page column 56; 58; 95, (2021/10/30)

The present disclosure relates to compounds of Formula (I) that modulate the activity of G-protein coupled receptor 52 (GPR52), pharmaceutically acceptable salts of compounds of Formula (I), and pharmaceutical compositions thereof. Compounds, pharmaceutic

TRIAZOLOPYRAZINE COMPOUNDS USEFUL FOR THE TREATMENT OF DEGENERATIVE & INFLAMMATORY DISEASES

-

, (2008/06/13)

Novel [1.2.4]triazolo[1,5-a]pyrazine compounds are disclosed that have a formula represented by the following (formula I). The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, arthritis, inflammation, and others.

Triazolopyridines. 18.1 nucleophilic substitution reactions on triazolopyridines; a new route to 2,2'-Bipyridines

Jones, Gurnos,Pitman, Mark A.,Lunt, Edward,Lythgoe, David J.,Abarca, Belen,Ballesteros, Rafael,Elmasnaouy, Mostafa

, p. 8257 - 8268 (2007/10/03)

The synthesis of some 5-, 6-, and 7-halogenotriazolopyridines is described and their reactions with nucleophiles. The formation or 7,7'-bitriazolopyridines provides a new synthesis of 2,2'-bipyridines.

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