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1,6-Heptadiene-3,5-dione, 4-(1,3-dithiolan-2-ylidene)-1,7-bis(4-methoxyphenyl)-, (1E,6E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

439661-91-3

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439661-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 439661-91-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,9,6,6 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 439661-91:
(8*4)+(7*3)+(6*9)+(5*6)+(4*6)+(3*1)+(2*9)+(1*1)=183
183 % 10 = 3
So 439661-91-3 is a valid CAS Registry Number.

439661-91-3Downstream Products

439661-91-3Relevant academic research and scientific papers

Highly facile and stereoselective intramolecular [2+2]photocycloadditions of bis(alkenoyl)ketenedithioacetals

Joseph, Bubbly K.,Verghese, Babu,Sudarsanakumar,Deepa,Viswam, Dhanya,Chandran, Prakash,Asokan

, p. 736 - 737 (2002)

The conformational change induced by the introduction of a ketenedithioacetal moiety at C-4 of 1,7-substituted-1,6-heptadiene-3,5-diones results in favorable spatial relationships between the alkenoyl groups to effect efficient intramolecular cycloadditio

Synthesis and crystal structure of 1,7-bis(4-methoxyphenyl)-4-(1,3- dithiolan-2-ylidene)-1,6-heptadiene-3,5-dione

Bubbly,Gudennavar,Viswam,Sudarsanakumar

, p. 175 - 179 (2011)

The synthesis and crystal structure of 1,7-bis(4-methoxyphenyl)-4-(1,3- dithiolan-2-ylidene)-1,6-heptadiene-3,5-dione is described. This compound crystallizes in the space group P21 with unit cell parameters a = 14.207 A, b = 7.752(1) A, c = 19

Efficient synthesis of substituted tetrahydrothiopyrano[2,3-b]thiopyran-4, 5-diones by a double annulation strategy from dialkenoylketene dithioacetals

Pan, Wei,Dong, Dewen,Ouyang, Yan,Wu, Rigenhada,Yang, Yang,Liu, Qun

, p. 2115 - 2120 (2008/03/12)

An efficient synthetic procedure for substituted 2,3,6,7- tetrahydrothiopyrano[2,3-b]thiopyran-4,5-diones by a double annulation strategy is described. The ring systems are made in good yields from readily available dialkenoylketene dithioacetals in the p

Facile and clean synthesis of α-alkenoyl ketene-(S,S)-acetals via the aldol condensation reactions in water

Ouyang, Yan,Dong, Dewen,Pan, Wei,Zhang, Jie,Liu, Qun

, p. 10111 - 10116 (2007/10/03)

The aldol condensation reactions of α,α-diacetyl ketene-(S,S)-acetals, 1a and 1b, with aromatic aldehydes 2 in the presence of NaOH in water have been investigated. At room temperature, the base-mediated condensations proceed smoothly to afford the corres

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