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β,β-Dideutero-3-phenylpropionylchlorid is a chemical compound with the molecular formula C9H8D2OCl. It is a deuterated analog of 3-phenylpropionyl chloride, where two hydrogen atoms are replaced by deuterium atoms. β,β-Dideutero-3-phenylpropionylchlorid is primarily used in organic synthesis, particularly in the preparation of isotopically labeled compounds for research purposes. The presence of deuterium atoms can provide valuable information about the reaction mechanisms and the stability of the resulting products. β,β-Dideutero-3-phenylpropionylchlorid is a colorless liquid with a pungent odor and is sensitive to moisture and light, requiring proper storage conditions to maintain its stability.

61233-29-2

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61233-29-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61233-29-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,3 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61233-29:
(7*6)+(6*1)+(5*2)+(4*3)+(3*3)+(2*2)+(1*9)=92
92 % 10 = 2
So 61233-29-2 is a valid CAS Registry Number.

61233-29-2Downstream Products

61233-29-2Relevant academic research and scientific papers

Ligand-Assisted Palladium(II)/(IV) Oxidation for sp3C H Fluorination

Sun, Huan,Zhang, Yi,Chen, Ping,Wu, Yun-Dong,Zhang, Xinhao,Huang, Yong

, p. 1946 - 1957 (2016)

The direct functionalization of inert sp3C H bonds is limited to a few bond types. Although the activation of sp3C H bonds can be accomplished under mild conditions using palladium catalysts, the subsequent functionalization is not trivial due to the high energy required to convert palladium(II) to palladium(IV). We have systematically studied the palladium oxidation using computation-guided experiments for reactions involving strong chelation control. We find that a mild external ligand could significantly accelerate the oxidation of palladium(II) to palladium(IV) for strong bidentate directing groups. The acceleration is believed to be a result of ligand stabilization of both the palladium(II) and palladium(IV) intermediates. (Figure presented.) .

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