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2-Chloro-3-benzyloxymethylpyridine, a pyridine derivative with the molecular formula C13H11ClNO, is a chemical compound characterized by the presence of a chlorine atom and a benzyloxy group attached to the second and third positions of the pyridine ring, respectively. It is commonly utilized in organic synthesis as a versatile building block for the preparation of pharmaceutical and agrochemical products, owing to its unique chemical properties and reactivity.

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  • 108082-72-0 Structure
  • Basic information

    1. Product Name: 2-CHLORO-3-BENZYLOXYMETHYLPYRIDINE
    2. Synonyms: 2-CHLORO-3-BENZYLOXYMETHYLPYRIDINE;PYRIDINE,2-CHLORO-3-(PHENYLMETHOXY)-
    3. CAS NO:108082-72-0
    4. Molecular Formula: C12H10ClNO
    5. Molecular Weight: 233.69348
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 108082-72-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 342.8°C at 760 mmHg
    3. Flash Point: 161.1°C
    4. Appearance: /
    5. Density: 1.225g/cm3
    6. Vapor Pressure: 0.000146mmHg at 25°C
    7. Refractive Index: 1.588
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. PKA: -0.54±0.10(Predicted)
    11. CAS DataBase Reference: 2-CHLORO-3-BENZYLOXYMETHYLPYRIDINE(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-CHLORO-3-BENZYLOXYMETHYLPYRIDINE(108082-72-0)
    13. EPA Substance Registry System: 2-CHLORO-3-BENZYLOXYMETHYLPYRIDINE(108082-72-0)
  • 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: 108082-72-0(Hazardous Substances Data)

108082-72-0 Usage

Uses

Used in Pharmaceutical Industry:
2-Chloro-3-benzyloxymethylpyridine is used as a key intermediate in the synthesis of various pharmaceutical compounds for its potential applications in medicine. Its unique chemical structure and reactivity make it a valuable component in the development of new drugs with improved therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Chloro-3-benzyloxymethylpyridine serves as a crucial building block in the preparation of agrochemical products, such as pesticides and herbicides. Its chemical properties contribute to the development of effective and environmentally friendly solutions for agricultural applications.
Used in Organic Synthesis:
2-Chloro-3-benzyloxymethylpyridine is employed as a versatile reagent in organic synthesis, enabling the creation of a wide range of chemical compounds with diverse applications across various industries. Its unique structure and reactivity facilitate the synthesis of complex molecules and contribute to the advancement of chemical research and development.
Used in Research and Development:
This chemical compound is also utilized in research and development settings, where its unique properties and reactivity are harnessed to explore new chemical reactions, mechanisms, and applications. 2-Chloro-3-benzyloxymethylpyridine plays a significant role in advancing scientific knowledge and fostering innovation in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 108082-72-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,0,8 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 108082-72:
(8*1)+(7*0)+(6*8)+(5*0)+(4*8)+(3*2)+(2*7)+(1*2)=110
110 % 10 = 0
So 108082-72-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H10ClNO/c13-12-11(7-4-8-14-12)15-9-10-5-2-1-3-6-10/h1-8H,9H2

108082-72-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-3-(phenylmethoxymethyl)pyridine

1.2 Other means of identification

Product number -
Other names 3-benzyloxy-2-chloropyridine

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:108082-72-0 SDS

108082-72-0Relevant articles and documents

Total synthesis of 4-epi-atpenin A5 as a potent nematode complex II inhibitor

Lee, Daiki,Kondo, Hiroki,Kuwayama, Yui,Takahashi, Kento,Arima, Shiho,Omura, Satoshi,Ohtawa, Masaki,Nagamitsu, Tohru

, p. 3178 - 3185 (2019)

It is clear that atpenins and their analogs are useful chemical tools for elucidation of complex II functionality and that they could act as lead compounds for the development of novel helminth complex II-specific inhibitors. Recently, we discovered 4-epi

METHOD FOR PRODUCING OXYPYRIDINE COMPOUND AND ATPENIN ANALOG

-

Paragraph 0108-0111, (2019/08/06)

PROBLEM TO BE SOLVED: To provide a method for producing an oxypyridine compound at low cost and/or with high efficiency. SOLUTION: A method for producing a compound represented by formula (I) [R1, R2, R3 and R4

TDO2 INHIBITORS

-

Paragraph 2208, (2017/07/14)

Presently provided are inhibitors of cellularly expressed TDO2 and pharmaceutical compositions thereof, useful for modulating an activity of tryptophan 2, 3 dioxygenase; treating immunosuppression; treating a medical conditions that benefit from the inhibition of tryptophan degradation; enhancing the effectiveness of an anti-cancer treatment comprising administering an anti-cancer agent; and treating tumor-specific immunosuppression associated with cancer.

2-AMINOPYRIDINE ANALOGS AS GLUCOKINASE ACTIVATORS

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Page/Page column 120, (2008/12/04)

Provided are compounds that are useful in the treatment and/or prevention of diseases mediated by deficient levels of glucokinase activity, such as diabetes mellitus. Also provided are methods of treating or preventing diseases and disorders characterized by underactivity of glucokinase or which can be treated by activating glucokinase.

3-`(HETERO) ARYLMETHOXY ! PYRIDINES AND THEIR ANALOGUES AS P38 MAP KINASE INHIBITORS

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Page/Page column 63-64; 66, (2010/11/30)

Compounds of the formula (I), wherein: -X=Y- is selected from -CR2=CR3- and -CR2=N-; R1 is selected from H, halo, NRR', NHC(=O)R, NHC(=O)NRR', NH2SO2R, and C(=O)NRR'; R2 and R3 (where present) are independently selected from H, optionally substituted C1-7 alkyl, optionally substituted C5-20 aryl, optionally substituted C3-20 heterocyclyl, halo, amino, amido, hydroxy, ether, thio, thioether, acylamido, ureido and sulfonamino; R4 is an optionally substituted C5-20 aryl or C5-20 heteroaryl group; and R5 is selected from R5’, halo, NHR5’, C(=O)NHR5’, OR5’, SR5’, NHC(=O)R5’, NHC(=O)NHR5’, NHS(=O)R5’, wherein R5’ is H or C1-3 alkyl (optionally substituted by halo, NH2, OH, SH) are disclosed for use in therapy and for treating diseases ameliorated by inhibiting p38 MAP kinase.

8-Piperazinyl-2,3-dihydro-1,4-dioxinopyridine Derivatives: Synthesis and Interaction with 5-HT Serotonin Binding Sites

Joseph, Benoit,Benarab, Abdelhakim,Guillaumet, Gerald

, p. 1355 - 1360 (2007/10/02)

The synthesis of 8-piperazinyl-2,3-dihydro-1,4-dioxinopyridine derivatives (6a-c) are described.Their affinity and selectivity for 5-HT serotoninergic sites were evaluated.

Zwitterionic Analogues of Cimetidine as H2 Receptor Antagonists

Young, Rodney C.,Ganellin, C. Robin,Graham, Michael J.,Mitchell, Robert C.,Roantree, Michael L.,Tashma, Zev

, p. 1150 - 1156 (2007/10/02)

A series of analogues of the H2 receptor histamine antagonist cimetidine have been synthesized in which the dipolar cyanoguanidine group has been replaced by a number of zwitterionic moieties.Although none of the compounds is more effective tha

2-[2-Thiazolyl or 2-guanidino-4-thiazolyl methylthioethyl(or butyl)amino]-3-(hydroxy or carboxy)pyridines, compositions containing same and method of use

-

, (2008/06/13)

This invention relates to 2-amino-3-hydroxy, and 3-carboxy pyridine derivatives, in which the amino group is substituted by a methylthioethyl, butyl or oxypropyl group bearing a terminal heterocyclic group. The compounds have histamine H2 -antagonist activity. A specific compound of this invention is 2-[2-(2-guanidino-4-thiazolylmethylthio)ethyl]amino pyridine 3-carboxylic acid.

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