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CAS

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35854-37-6

4-[(3-Methoxyphenyl)methyl]pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 35854-37-6 Structure

  • Basic information

    1. Product Name: 4-[(3-Methoxyphenyl)methyl]pyridine
    2. Synonyms: 4-[(3-Methoxyphenyl)methyl]pyridine
    3. CAS NO:35854-37-6
    4. Molecular Formula: C13H13NO
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 35854-37-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-[(3-Methoxyphenyl)methyl]pyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-[(3-Methoxyphenyl)methyl]pyridine(35854-37-6)
    11. EPA Substance Registry System: 4-[(3-Methoxyphenyl)methyl]pyridine(35854-37-6)

  • 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: 35854-37-6(Hazardous Substances Data)

35854-37-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35854-37-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,8,5 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 35854-37:
(7*3)+(6*5)+(5*8)+(4*5)+(3*4)+(2*3)+(1*7)=136
136 % 10 = 6
So 35854-37-6 is a valid CAS Registry Number.

35854-37-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(3-methoxyphenyl)methyl]pyridine

1.2 Other means of identification

Product number -
Other names Pyridine,4-[(3-methoxyphenyl)methyl]

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:35854-37-6 SDS

35854-37-6Relevant articles and documents

Synthesis of 4-benzylpyridines via Pd-catalyzed CH3-arylation of 4-picoline

Wu, Jing,Wang, Dadian,Chen, Xiang,Gui, Qingwen,Li, Hua,Tan, Ze,Huang, Genping,Wang, Guangwei

supporting information, p. 7509 - 7512 (2017/09/27)

A highly efficient synthesis of 4-benzylpyridines was developed via Pd-catalyzed C(sp3)-H arylation between 4-picoline and aryl halides. It was found that the best yields were achieved with a simple Pd(PPh3)4 catalyst and Cs2CO3 as the base. Compared with the known methods, our reaction does not require the use of a strong organometallic reagent as the base.

3-alkoxybenzylpiperidine derivatives as melatonergic agents

-

, (2008/06/13)

Novel 3-alkoxybenzylpiperidines have melatonergic properties. They are believed useful in treating depression, jet-lag, work-shift syndrome, sleep disorders, glaucoma, some disorders associated with reproduction, cancer, immune disorders and neuroendocrin

PIPERAZINYL-AND PIPERIDINYL-CYCLOHEXANOLS

-

, (2008/06/13)

Novel piperazinyl-and piperidinyl-cyclohexanols of the following formula are useful as anxiolytic agents and have other psychotropic properties STR1

Mercuric acetate cyclization of 4-(arylmethyl)piperidines: Synthesis of indolo[2,3-g]morphans (tetracyclic ring system of strychnos indole alkaloids) and 7,8-benzomorphans

Bosch,Bonjoch,Diez,et al.

, p. 1753 - 1762 (2007/10/02)

A new synthetic route to indolo[2,3-g]morphans and 7,8-benzomorphans is reported. The key step in these syntheses is the mercuric acetate oxidation of appropriate 2-(4-piperidyl-methyl)indoles or 4-benzylpiperidines, respectively. An alternative synthetic

Bridged-ring Nitrogen Compounds. Part 5. Synthesis of 2,6-Methano-3-benzazonine ring-system

Proctor, George R.,Smith, Francis J.

, p. 1754 - 1762 (2007/10/02)

Syntheses of cis- and trans-4-benzyl- and 4-(3-methoxybenzyl)-2-methoxycarbonyl-1-methylpiperidines are described; amino-acids and amino-alcohols obtained from these compounds failed to cyclise. cis-2-Benzyl-4-ethoxycarbonyl-1-methylpiperidine has been ma

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