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3-chloro-2-cyclopropylpyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1355066-87-3 Structure
  • Basic information

    1. Product Name: 3-chloro-2-cyclopropylpyridine
    2. Synonyms: 3-chloro-2-cyclopropylpyridine
    3. CAS NO:1355066-87-3
    4. Molecular Formula: C8H8ClN
    5. Molecular Weight: 153.60882
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1355066-87-3.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: 3-chloro-2-cyclopropylpyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-chloro-2-cyclopropylpyridine(1355066-87-3)
    11. EPA Substance Registry System: 3-chloro-2-cyclopropylpyridine(1355066-87-3)
  • 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: 1355066-87-3(Hazardous Substances Data)

1355066-87-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1355066-87-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,5,0,6 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1355066-87:
(9*1)+(8*3)+(7*5)+(6*5)+(5*0)+(4*6)+(3*6)+(2*8)+(1*7)=163
163 % 10 = 3
So 1355066-87-3 is a valid CAS Registry Number.

1355066-87-3Relevant articles and documents

Chemoselective sp 2-sp3 cross-couplings: Iron-catalyzed alkyl transfer to dihaloaromatics

Malhotra, Sushant,Seng, Pamela S.,Koenig, Stefan G.,Deese, Alan J.,Ford, Kevin A.

supporting information, p. 3698 - 3701 (2013/08/23)

The chemoselective functionalization of a range of dihaloaromatics with methyl, cyclopropyl, and higher alkyl Grignard reagents via iron-catalyzed cross-coupling is described. The site selectivity of C-X (X = halogen) activation is determined by factors such as the position of the halogen on the ring, the solvent, and the nucleophile. A one-pot protocol for the chemoselective synthesis of mixed dialkyl heterocycles is achieved solely employing iron catalysis.

CHEMICAL COMPOUNDS

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Page/Page column 87-88, (2012/02/02)

PC71695A Abstract Chemical Compounds The invention relates to sulfonamide derivatives, to their use in medicine, to 5 compositions containing them, to processes for their preparation and to intermediates used in such processes. More particularly the invention relates to a new sulfonamide Nav1.7 inhibitors of formula (I):10 X NH O S O O R1 R2 R5 R4 R3 Het1 (I) or a pharmaceutically acceptable salt thereof, wherein X, Het1, R1, R2, R3, R4 and R5 are as defined in the description. 15 Nav 1.7 inhibitors are potentially useful in the treatment of a wide range of disorders, particularly pain.

CHEMICAL COMPOUNDS

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Page/Page column 76-77, (2012/02/02)

The invention relates to sulfonamide derivatives, to their use in medicine, to compositions containing them, to processes for their preparation and to intermediates used in such processes. More particularly the invention relates to a new sulfonamide Nav1.7 inhibitors of formula 10 (I): (I) or a pharmaceutically acceptable salt thereof, wherein Z, R 1, R2, R3, R4 and R5 are as defined in the description. Nav 1.7 inhibitors are potentially useful in the treatment of a wide range of disorders, particularly pain.

CHEMICAL COMPOUNDS

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Page/Page column 52, (2012/01/15)

The invention relates to sulfonamide derivatives, to their use in medicine, to compositions containing them, to processes for their preparation and to intermediates used in such processes. More particularly the invention relates to a new sulfonamide Nav1.7 inhibitors of formula (I): or a pharmaceutically acceptable salt thereof, wherein Het1, X, R1, R2, R3, R4 and R5 are as defined in the description. Nav 1.7 inhibitors are potentially useful in the treatment of a wide range of disorders, particularly pain

INDAZOLE DERIVATIVES AS SODIUM CHANNEL INHIBITORS

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Page/Page column 109-110, (2012/07/28)

The invention relates to acyl sulfonamide derivatives, to their use in medicine, to compositions containing them, to processes for their preparation and to intermediates used in such processes. More particularly the invention relates to a new acyl sulfona

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