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1225432-54-1

(Z)-2-bromo-1-phenyl-n-hept-1-en-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1225432-54-1 Structure

  • Basic information

    1. Product Name: (Z)-2-bromo-1-phenyl-n-hept-1-en-3-one
    2. Synonyms: (Z)-2-bromo-1-phenyl-n-hept-1-en-3-one
    3. CAS NO:1225432-54-1
    4. Molecular Formula:
    5. Molecular Weight: 267.166
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1225432-54-1.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: (Z)-2-bromo-1-phenyl-n-hept-1-en-3-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (Z)-2-bromo-1-phenyl-n-hept-1-en-3-one(1225432-54-1)
    11. EPA Substance Registry System: (Z)-2-bromo-1-phenyl-n-hept-1-en-3-one(1225432-54-1)

  • 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: 1225432-54-1(Hazardous Substances Data)

1225432-54-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1225432-54-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,5,4,3 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1225432-54:
(9*1)+(8*2)+(7*2)+(6*5)+(5*4)+(4*3)+(3*2)+(2*5)+(1*4)=121
121 % 10 = 1
So 1225432-54-1 is a valid CAS Registry Number.

1225432-54-1Downstream Products

1225432-54-1Relevant articles and documents

Vanadium-Catalyzed Synthesis of Geometrically Defined Acyclic Tri- and Tetrasubstituted Olefins from Propargyl Alcohols

Trost, Barry M.,Tracy, Jacob S.

, p. 1584 - 1594 (2019/02/05)

A highly selective formation of geometrically defined acyclic tri- and tetrasubstituted alkenes from inexpensive and readily available propargyl alcohols is described. Through vanadium oxo catalysis, tri- and tetrasubstituted α-chloro-, bromo-, and iodo-e

"Silver effect" in gold(I) catalysis: An overlooked important factor

Wang, Dawei,Cai, Rong,Sharma, Sripadh,Jirak, James,Thummanapelli, Sravan K.,Akhmedov, Novruz G.,Zhang, Hui,Liu, Xingbo,Petersen, Jeffrey L.,Shi, Xiaodong

scheme or table, p. 9012 - 9019 (2012/07/02)

Clear experimental evidence from X-ray photoelectron spectroscopy and 31P NMR spectroscopy has been obtained for the first time to confirm that the combination of Ag+ cation with [L-Au]+ results in the formation of different complexes in solution. Re-evaluation of literature-reported gold-catalyzed reactions revealed a significant difference in the reactivities with and without silver. In extreme cases (more than "rare"), the conventional [L-Au]+ catalysts could not promote the reaction without the presence of silver. This investigation has therefore revealed a long-overlooked "silver effect" in gold catalysis and should lead to revision of the actual mechanism.

Efficient synthesis of e -α-haloenones through chemoselective alkyne activation over allene with triazole-Au catalysts

Wang, Dawei,Ye, Xiaohan,Shi, Xiaodong

supporting information; experimental part, p. 2088 - 2091 (2010/07/03)

Figure presented The E-α-haloenones were prepared through a triazole-Au complex (TriA-Au) catalyzed propargyl acetate rearrangement and sequential allene halogenation. The reactions proceeded with only 1% catalyst loading, giving the challenging kinetic p

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