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1182190-94-8

2-(2-chloro-6-methoxyphenyl)pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1182190-94-8 Structure

  • Basic information

    1. Product Name: 2-(2-chloro-6-methoxyphenyl)pyridine
    2. Synonyms: 2-(2-chloro-6-methoxyphenyl)pyridine
    3. CAS NO:1182190-94-8
    4. Molecular Formula:
    5. Molecular Weight: 219.671
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1182190-94-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(2-chloro-6-methoxyphenyl)pyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2-chloro-6-methoxyphenyl)pyridine(1182190-94-8)
    11. EPA Substance Registry System: 2-(2-chloro-6-methoxyphenyl)pyridine(1182190-94-8)

  • 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: 1182190-94-8(Hazardous Substances Data)

1182190-94-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1182190-94-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,2,1,9 and 0 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1182190-94:
(9*1)+(8*1)+(7*8)+(6*2)+(5*1)+(4*9)+(3*0)+(2*9)+(1*4)=148
148 % 10 = 8
So 1182190-94-8 is a valid CAS Registry Number.

1182190-94-8Relevant articles and documents

Copper(II)-Promoted Mono-Selective ortho C-H Chlorination of Arenes by Using Trimethyl(trichloromethyl)silane

Zhu, Zhaobin,Xu, Changming,Wang, Yongchang,Zhao, Li

, p. 1122 - 1124 (2018/02/26)

The first example of a Cu-promoted ortho -chlorination of aryl C-H bonds by using TMSCCl 3 as chlorinating agent is reported. This reaction features a high selectivity toward monochlorination over dichlorination, compatibility with a variety of

Ligandless Nickel-Catalyzed Ortho-Selective Directed Trifluoromethylthiolation of Aryl Chlorides and Bromides Using AgSCF3

Nguyen, Tin,Chiu, Weiling,Wang, Xinying,Sattler, Madeleine O.,Love, Jennifer A.

supporting information, p. 5492 - 5495 (2016/11/17)

A mild protocol for Ni-catalyzed trifluoromethylthiolation of aryl chlorides and bromides is described herein. The method utilizes AgSCF3 as an easily accessible nucleophilic trifluoromethylthiolating reagent and does not require any ligands or additives. Ortho-selectivity is achieved using a variety of directing groups such as imines, pyridines, and oxazolines for 24 examples in up to 95% yield.

Arylmethyl chlorides: New bifunctional reagents for palladium-catalyzed ortho -chlorination and acylation of 2-arylpyridines

Zhang, Guodong,Sun, Suyan,Yang, Fan,Zhang, Qian,Kang, Jianxun,Wu, Yusheng,Wu, Yangjie

, p. 443 - 450 (2015/02/19)

A chemoselective, palladium-catalyzed, ligand-directed ortho-C-H chlorination and acylation process has been developed, exhibiting high regioselectivity for 2-arylpyridines bearing a meta-substituent. Worthy of note is the fact that arylmethyl chlorides a

Copper(II)-catalyzed ortho-functionalization of 2-arylpyridines with acyl chlorides

Wang, Wenhui,Pan, Changduo,Chen, Fan,Cheng, Jiang

supporting information; experimental part, p. 3978 - 3980 (2011/05/02)

Copper-catalyzed ortho-benzoxylation of 2-arylpyridine sp2 C-H bonds with acyl chloride is described. Notably, switching the base from t-BuOK to Li2CO3 causes chlorination of the C-H bond to take place. The Royal Society of Chemistry.

Palladium-catalyzed aromatic C-H halogenation with hydrogen halides by means of electrochemical oxidation

Kakiuchi, Fumitoshi,Kochi, Takuya,Mutsutani, Hitoshi,Kobayashi, Noboru,Urano, Seiya,Sato, Mitsuo,Nishiyama, Shigeru,Tanabe, Takamasa

supporting information; experimental part, p. 11310 - 11311 (2011/02/26)

(Chemical Equation Presented) A new strategy for catalytic functionalization of C-H bonds by means of electrochemical oxidation is described. Combination of palladium-catalyzed aromatic C-H bond cleavage and halogenation with electrochemically generated h

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