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(1-deuteriobutyl)benzene is an organic compound consisting of a benzene ring with a 1-deuteriobutyl group attached to it. The 1-deuteriobutyl group is a butyl chain with one deuterium atom (an isotope of hydrogen with one proton and one neutron) replacing a hydrogen atom at the first carbon position. (1-deuteriobutyl)benzene can be represented as C6H5-CH2-CD2-CH2-CH3, where the deuterium atom is indicated by the symbol "D" or "2H". It is a derivative of toluene, with a deuterium atom incorporated into the alkyl chain, which can be useful in various chemical reactions and studies, particularly in the field of isotope labeling and tracer experiments.

4397-69-7

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4397-69-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4397-69-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,9 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4397-69:
(6*4)+(5*3)+(4*9)+(3*7)+(2*6)+(1*9)=117
117 % 10 = 7
So 4397-69-7 is a valid CAS Registry Number.

4397-69-7Downstream Products

4397-69-7Relevant academic research and scientific papers

Method for constructing carbon-hydrogen bond by catalyzing alcohol dehydroxylation with palladium/platinum

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Paragraph 0114-0117, (2019/12/25)

The invention discloses a method for constructing a carbon-hydrogen (deuterium) bond. The method comprises the following step: in the presence of a palladium/platinum catalyst and aryl halide, an alcohol hydroxyl group of an alcohol and hydrogen (deuterium) gas is replaced by hydrogen (deuterium) to construct the carbon-hydrogen (deuterium) bond. According to the method, the palladium/platinum catalyst is used as a catalyst, the green hydrogen (deuterium) gas is used as a hydrogen (deuterium) source, efficient alcohol dehydroxylation is performed at room temperature to construct the carbon-hydrogen (deuterium) bond, and the method is particularly suitable for constructing the carbon-deuterium bond and can be widely applied to synthesis of deuterated drugs.

Alkylation of pyridines at their 4-positions with styrenes plus yttrium reagent or benzyl grignard reagents

Mizumori, Tomoya,Hata, Takeshi,Urabe, Hirokazu

supporting information, p. 422 - 426 (2015/02/19)

A new regioselective alkylation of pyridines at their 4-position was achieved with styrenes in the presence of yttrium trichloride, BuLi, and diisobutylaluminium hydride (DIBAL-H) in THF. Alternatively, similar products were more simply prepared from pyridines and benzyl Grignard reagents. These reactions are not only a useful preparation of 4-substituted pyridines but are also complementary to other relevant reactions usually giving 2-substituted pyridines.

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