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(Z)-4-methyl-3-decen-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82235-24-3

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82235-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82235-24-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,2,3 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82235-24:
(7*8)+(6*2)+(5*2)+(4*3)+(3*5)+(2*2)+(1*4)=113
113 % 10 = 3
So 82235-24-3 is a valid CAS Registry Number.

82235-24-3Downstream Products

82235-24-3Relevant academic research and scientific papers

PALLADIUM-CATALYZED ACYLATION OF ORGANOZINCS AND OTHER ORGANOMETALLICS AS A CONVENIENT ROUTE TO KETONES

Negishi, Ei-ichi,Bagheri, Vahid,Chatterjee, Sugata,Luo, Fen-Tair,Miller, Joseph A.,Stoll, A. Timothy

, p. 5181 - 5184 (1983)

The reaction of organozincs with acyl chlorides catalyzed by palladium-phosphine complexes, e.g., Pd(PPh3)4, provides a highly general and convinient route to ketones.

An entry to non-racemic β-tertiary-β-amino alcohols, building blocks for the synthesis of aziridine, piperazine, and morpholine scaffolds

Narczyk, Aleksandra,Stecko, Sebastian

supporting information, p. 5972 - 5981 (2020/08/21)

A method for the preparation of enantiopure β-tert-amino alcohols bearing a tetrasubstituted C-stereocenter, as well as their conversion into selected medicinally privileged heterocyclic systems (morpholines, aziridines, piperazines) is reported. These co

ALDOL-TYPE REACTIONS BETWEEN TRIMETHYLSILYL ENOL ETHERS AND ACETALS WITH THE AID OF RHODIUM COMPLEX

Sato, Susumu,Matsuda, Isamu,Izum, Yusuke

, p. 6657 - 6660 (2007/10/02)

Aldol type reactions of trimethylsilyl enol ethers with acetals, ketals and orthoesters are successfully performed with the aid of a catalytic amount of rhodium complex Rh4(CO)12 or (Rh(COD)(DPPB))(1+)*ClO4(1-), under neutral conditions.

A NEW PROCEDURE FOR DESULFONYLATION: PREPARATION OF β-SUBSTITUTED α,β-UNSATURATED KETONES AND ALDEHYDES

Yoshida, Takashi,Saito, Shojiro

, p. 165 - 168 (2007/10/02)

The treatment of the tert-alkyl sulfones bearing carbonyl group at the β-position with 5 percent hydrochloric acid in THF at 30 - 65 deg C afforded β-substituted α,β-unsaturated ketones and aldehydes in excellent yields.

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