Welcome to LookChem.com Sign In|Join Free
  • or
(3S)-3-(tert-butyldimethylsilanyloxy)-4-trityloxybutyraldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

950588-69-9

Post Buying Request

950588-69-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

950588-69-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 950588-69-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,0,5,8 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 950588-69:
(8*9)+(7*5)+(6*0)+(5*5)+(4*8)+(3*8)+(2*6)+(1*9)=209
209 % 10 = 9
So 950588-69-9 is a valid CAS Registry Number.

950588-69-9Relevant academic research and scientific papers

Total synthesis and absolute configuration of koshikalide

Kunifuda, Kazuki,Iwasaki, Arihiro,Nagamoto, Masashi,Suenaga, Kiyotake

, p. 3121 - 3123 (2016)

The first total synthesis of koshikalide, a 14-membered macrolide that contains three olefins, was achieved. The skipped diene in the cyclic system was efficiently constructed by very mild Stille coupling at low temperature. The absolute stereochemistry was established by comparison of the specific optical rotations of natural and synthesized koshikalide.

Total synthesis of solandelactones A, B, E, and F exploiting a tandem petasis-claisen lactonization strategy

White, James D.,Lincoln, Christopher M.,Yang, Jongtae,Martin, William H. C.,Chan, David B.

, p. 4139 - 4150 (2008/09/20)

(Chemical Equation Presented) Solandelactones A, B, E, and F were synthesized using Nozaki-Hiyama-Kishi coupling of iododiene 13 with aldehydes 14 and 99 obtained by oxidation of alcohols 92 and 94. Key steps in the synthesis of 92 and 94 were (i) a Nagao asymmetric acetate aldol reaction of aldehyde 77 with thionothiazolidine 78 to set in place an alcohol that becomes the (75) lactone center of solandelactones, (ii) a Simmons-Smith cyclopropanation of 80 directed by this alcohol, and (iii) Petasis methylenation of cyclic carbonate 90 in tandem with a Claisen rearrangement that generates the octenalactone portion of solandelactones. Synthesis of solandelactones A, B, E, and F confirmed their gross structure and absolute configuration at C7, 8, 10, and 14 but showed that alcohol configuration at C11 must be reversed in pairs, A/B and E/F, from the previous assignment made to these hydroid metabolites. Thus, solandelactones A and B are correctly represented by 2 and 1, respectively, whereas solandelactones E and F are 6 and 5. A biogenesis of solandelactones is proposed for these C22 oxylipins that parallels a hypothesis put forward previously to explain the origin of C20 cyclopropane-containing algal products.

Total synthesis of solandelactones E and F, homoeicosanoids from the hydroid Solanderia secunda

White, James D.,Martin, William H.C.,Lincoln, Christopher,Yang, Jongtae

, p. 3481 - 3483 (2008/02/12)

Asymmetrie total syntheses of solandelactones E and F confirmed that hydroxyl configuration at C11 in these oxylipins had been misassigned and that the stereochemistry at this center should be reversed. Key steps in the synthesis involved a Nagao asymmetr

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 950588-69-9