Welcome to LookChem.com Sign In|Join Free
  • or
(2R,3R)-2,3-Bis-[2-(2-benzyloxy-ethoxy)-ethoxy]-2,3-bis-[2-(2-benzyloxy-ethoxy)-ethyl]-succinic acid diethyl ester is a complex organic compound with a molecular formula of C42H62O12. It is a chiral molecule, meaning it has a non-superimposable mirror image, and is characterized by its 2R,3R configuration. (2R,3R)-2,3-Bis-[2-(2-benzyloxy-ethoxy)-ethoxy]-2,3-bis-[2-(2-benzyloxy-ethoxy)-ethyl]-succinic acid diethyl ester features a succinic acid core, which is esterified with diethyl groups, and has four ethoxy chains, each terminated with a benzyloxy group. The presence of these benzyloxy-ethoxy-ethoxy chains suggests that (2R,3R)-2,3-Bis-[2-(2-benzyloxy-ethoxy)-ethoxy]-2,3-bis-[2-(2-benzyloxy-ethoxy)-ethyl]-succinic acid diethyl ester may be used in applications where solubility or reactivity with other molecules is desired, such as in pharmaceuticals or materials science. The specific arrangement of these functional groups could influence its physical properties and potential uses, although further context or application details would be needed to fully understand its significance.

88475-84-7

Post Buying Request

88475-84-7 Suppliers

Recommended suppliers

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

88475-84-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88475-84-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,7 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88475-84:
(7*8)+(6*8)+(5*4)+(4*7)+(3*5)+(2*8)+(1*4)=187
187 % 10 = 7
So 88475-84-7 is a valid CAS Registry Number.

88475-84-7Downstream Products

88475-84-7Relevant academic research and scientific papers

Synthesis of Lipophilic 18-Crown-6 Diacids for the Membrane Transport of Alkaline-Earth Cations

Fyles, Thomas M.,McGavin, Cynthia A.,Whitfield, Dennis M.

, p. 753 - 761 (2007/10/02)

The synthesis of three different types of lipophilic 18-crown-6 diacids is described.A didecyl crown ether 2,3-diacid (1) was prepared as a minor product from a diiodide precursor (12) and threo-11,12-docosanediol by thallous ethoxide cyclization.The major nonpolymeric products resulted from elimination followed by cyclization to give 15-crown-5-derivatives.A crown ether 11,12-diamide 2,3-diacid (4) was prepared by a similar route involving cyclization of a benzyl protected precursor (26) and N,N,N',N'-tetramethyltartaramide (9).Isomeric syn and anti 2,11(12)-diamide 3,12(11)-diacid derivatives 6 and 7 were prepared from the known crown ether bisanhydride 8 and alkylamines.The product mixture was separated by chromatography, and the isomers were identified by comparison of acidity and stability constants for complexation with those of closely related syn/anti crown ether acids.

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 88475-84-7