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2-bromo-1-cyclohexene-1-carbonyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 159389-47-6 Structure
  • Basic information

    1. Product Name: 2-bromo-1-cyclohexene-1-carbonyl chloride
    2. Synonyms: 2-bromo-1-cyclohexene-1-carbonyl chloride
    3. CAS NO:159389-47-6
    4. Molecular Formula:
    5. Molecular Weight: 223.497
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 159389-47-6.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-bromo-1-cyclohexene-1-carbonyl chloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-bromo-1-cyclohexene-1-carbonyl chloride(159389-47-6)
    11. EPA Substance Registry System: 2-bromo-1-cyclohexene-1-carbonyl chloride(159389-47-6)
  • 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: 159389-47-6(Hazardous Substances Data)

159389-47-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 159389-47-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,3,8 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 159389-47:
(8*1)+(7*5)+(6*9)+(5*3)+(4*8)+(3*9)+(2*4)+(1*7)=186
186 % 10 = 6
So 159389-47-6 is a valid CAS Registry Number.

159389-47-6Relevant articles and documents

Access to Cyclopropyl-Fused Azacycles via a Palladium-Catalyzed Direct Alkenylation Strategy

Ladd, Carolyn L.,Charette, André B.

, p. 6046 - 6049 (2016)

Palladium-catalyzed direct alkenylation of cyclopropyl C-H bonds proceeds in high efficiency. This transformation provides access to novel cyclopropyl-fused azacycles. Ligand studies suggest that bisphosphine monoxide analogues of dppf and rac-BINAP are t

Palladium(0)-catalyzed asymmetric C-H alkenylation for efficient synthesis of planar chiral ferrocenes

Gao, De-Wei,Gu, Yiting,Wang, Shao-Bo,Gu, Qing,You, Shu-Li

, p. 3227 - 3233 (2016)

Pd(0)-catalyzed intramolecular C-H alkenylation was achieved with excellent yields and enantioselectivity for the construction of planar chiral ferrocenes. It is compatible with a broad range of substrates and various functional groups. Notably, the enant

A general strategy for visible-light decaging based on the quinone: Cis -alkenyl lock

Walton, David P.,Dougherty, Dennis A.

supporting information, p. 4965 - 4968 (2019/05/21)

Combining the fast thermal cyclization of o-coumaric acid derivatives with the intramolecular photoreduction of quinones gives new visible-light photoremovable protecting groups absorbing well above 450 nm.

Diastereoselective palladium-catalyzed arylcyanation/heteroarylcyanation of enantioenriched N -allylcarboxamides

Yoon, Hyung,Petrone, David A.,Lautens, Mark

supporting information, p. 6420 - 6423 (2015/02/05)

A diastereoselective Pd-catalyzed arylcyanation/heteroarylcyanation of chiral N-allylcarboxamides using Zn(CN)2 as the cyanide source is reported. Nitrile-containing dihydroisoquinolinone products are obtained in good to excellent yields with u

CuI/amino acid-catalyzed coupling and cyclization of β-bromo-α, β-unsaturated amides with terminal alkynes leading to (3Z)-3- alkylidenepyrrol-1-ones

Son, Jong Ik,Cho, Chan Sik,Choi, Heung-Jin

, p. 380 - 386 (2013/07/26)

β-Bromo-α,β-unsaturated amides are coupled and cyclized with terminal alkynes in DMF at 110 °C in the presence of a catalytic amount of CuI and amino acid along with a base to give the corresponding (3Z)-3-alkylidenepyrrol-1-ones in moderate to good yield

Chemoselective benzylic C-H activations for the preparation of condensed N-heterocycles

Ren, Hongjun,Knochel, Paul

, p. 3462 - 3465 (2007/10/03)

Buttoning up: A chemoselective domino reaction including one or two successive C-H activations serves to convert a range of readily available N-arylpyrroles into complex polycondensed N-heterocycles. The reaction is catalyzed by Pd(OAc)2 (5 mol%), and p-Tol3P (10 mol%) is added as the ligand (see scheme; Tol = tolyl).

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