185996-33-2 Usage
General Description
(S)-2,2-Dimethyl-1,3-dioxolane-4-acetamide, also known as DMDOA, is a chemical compound with the molecular formula C8H15NO2. It is an acetamide derivative with a cyclic structure, containing a dioxolane group. (S)-2,2-DIMETHYL-1,3-DIOXOLANE-4-ACETAMIDE is used in organic synthesis and pharmaceutical research as a building block for the synthesis of various pharmaceutical compounds and other organic molecules. It is also used as a reagent in chemical reactions and as a chiral auxiliary in asymmetric synthesis. Additionally, DMDOA has potential applications in the production of drugs and other bioactive compounds due to its unique chemical structure and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 185996-33-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,9,9 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 185996-33:
(8*1)+(7*8)+(6*5)+(5*9)+(4*9)+(3*6)+(2*3)+(1*3)=202
202 % 10 = 2
So 185996-33-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H13NO3/c1-7(2)10-4-5(11-7)3-6(8)9/h5H,3-4H2,1-2H3,(H2,8,9)/t5-/m0/s1
185996-33-2Relevant articles and documents
PROCESS FOR THE PREPARATION OF PROTECTED DIHYDROXYPROPYL TRIALKYLAMMONIUM SALTS AND DERIVATIVES THEREOF
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Page/Page column 7; 8-9, (2008/06/13)
A process for the preparation of protected dihydroxypropyl trialkylammonium salts, particularly in chiral form is described. In particular, a process for the preparation of (2,2-dimethyl-1,3-dioxolan-4-ylmethyl)trialkylammonium salts, particularly in chiral form is described. Furthermore, a process is described wherein the (2,2-dimethyl-1,3-dioxolan-4ylmethyl)trialkylammonium salts is a 2,2-dimethyl-1,3-dioxolan-4-ylmethyl trimethylammonium salt, preferably in chiral form. The protected dihydroxypropyl trialkylammonium salts lead to L-carnitine (9) when in chiral form (5).
Synthetic studies towards pateamine, a novel thiazole-based 19-membered bis-lactone from Mycale sp
Critcher, Douglas J.,Pattenden, Gerald
, p. 9107 - 9110 (2007/10/03)
A concise synthesis of the 19-membered bis-lactone core 2b present in pateamine 1 using chiral pool starling materials and featuring an intramolecular Stille coupling reaction as a key stratagem, is described. Copyright (C) 1996 Elsevier Science Ltd.
