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1-Butanone, 2,3-dibromo-3-methyl-1-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64097-38-7

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64097-38-7 Usage

Physical state

Colorless to pale yellow liquid

Odor

Strong, pungent

Usage

a. Organic synthesis
b. Intermediate in pharmaceuticals and agrochemicals production
c. Reagent in flavors and fragrances production

Hazardous nature

Can cause irritation to skin, eyes, and respiratory system

Safety precautions

Handle with care due to its hazardous nature

Check Digit Verification of cas no

The CAS Registry Mumber 64097-38-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,0,9 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 64097-38:
(7*6)+(6*4)+(5*0)+(4*9)+(3*7)+(2*3)+(1*8)=137
137 % 10 = 7
So 64097-38-7 is a valid CAS Registry Number.

64097-38-7Relevant academic research and scientific papers

Synthesis of α,β-dibromo ketones by photolysis of α-bromo ketones with N-bromosuccinimide: Photoinduced β-bromination of α-bromo ketones

Moon, Da Yoon,An, Sejin,Park, Bong Ser

, (2019/10/28)

Irradiation of α-bromopropiophenones in the presence of NBS results in the formation of α,β-dibromopropiophenones, which can be viewed as β-bromination of α-bromopropiophenones. The reaction is believed to go through a series of reactions; photoinduced C–Br bond cleavage, elimination of HBr to give α,β-unsaturated ketone intermediates, and addition of Br2, which are formed by the reaction between HBr and NBS. From mechanistic studies of the reaction, we have also found a very convenient method for α-debromination of the α,β-dibromopropiophenones which is by simple irradiation of the dibromo ketones in acetone or 2-propanol without the use of any additives. Our results demonstrate that bromine can be added into or eliminated from the alpha, beta, or both positions to the carbonyl group by photochemical methods, which make synthetic options of bromine containing carbonyl compounds versatile.

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