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(3RS,6RS)-3,6-dimethoxy-cyclohexene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21410-29-7

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21410-29-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21410-29-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,1 and 0 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 21410-29:
(7*2)+(6*1)+(5*4)+(4*1)+(3*0)+(2*2)+(1*9)=57
57 % 10 = 7
So 21410-29-7 is a valid CAS Registry Number.

21410-29-7Downstream Products

21410-29-7Relevant academic research and scientific papers

D-proline derivatives

-

, (2008/06/13)

New compounds have the formula: wherein R, R1, X and Y have the meanings described herein. Methods are set forth for synthesizing these compounds and using these compounds to treat diseases associated with amyloidosis, such as Alzheimer's disease, maturity onset diabetes mellitus, familial amyloid polyneuropathy, scrapie, and Kreuzfeld-Jacob disease.

Regio- and Stereo-Controlled Alkoxyiodination of 1,3-Diene Using Iodine-Cerium(IV) Ammonium Nitrate

Horiuchi, C. Akira,Hosokawa, Haruomi,Kanamori, Miyuki,Muramatsu, Yukiko,Ochiai, Keiko,Takahashi, Eiji

, p. 13 - 14 (2007/10/02)

Reaction of 1,3-cycloalkadienes (cyclopentadiene, cyclohexadiene, and cycloheptadiene) with iodine-cerium(IV) ammonium nitrate in alcohols, gave the corresponding regiospecific trans-2-alkoxy-1-iodo compounds as major products accompanied with 1,4-dialkoxy compounds as by-products.In the case of CH3CN-H2O as solvent, trans-iodohydrins were obtained.Thus the reaction of cyclic and acyclic i671,3-diene derivatives using this synthetic method afforded the 1,2-addition alkoxyiodo compounds preferentially.

VINYL MIGRATION IN THE OXYTHALLATION OF SOME 1,3-DIENES

Murakami, Masashi,Nishida, Shinya

, p. 997 - 1000 (2007/10/02)

The oxythallation of certain 1,3-dienes with thallium (III) nitrate trihydrate in MeOH-CH2Cl2 at 0-20 deg C gave products after vinyl migration .Methyl 1-methylcyclopropyl ketone, obtained in the reaction of 2,3-dimethyl-1,3-butadiene, was presumably derived from a cyclopropylmethyl cation, an intermediate in the vinyl migration.

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